New Model Links Brain Aging to Disrupted DNA Repair Rhythm and TyrRS Switch
A theoretical model published 17 September in GeroScience ties together two hallmarks of brain aging: the buildup of DNA damage in neurons and the weakening of circadian rhythms. The authors propose the enzyme tyrosyl‑tRNA synthetase (TyrRS) as a molecular switch that coordinates both processes and explain why they falter together in aging and Alzheimer’s disease.
TyrRS normally charges tyrosine onto tRNA for protein synthesis, but when free tyrosine is low — during the night or fasting — a fraction translocates to the nucleus. There it activates PARP1 to detect DNA breaks, keeps transposable‑element DNA silenced to prevent inflammation, and induces the LIN9 gene. LIN9 joins the DREAM complex, which by day represses 67 DNA‑repair genes (including BRCA1) and releases them at night for repair.
The oscillation amplitude of these three activities matters more than their average level. With age, blood tyrosine rises 15–25%, narrowing the nighttime window for TyrRS action, while suprachiasmatic‑nucleus neuron loss dampens circadian rhythms. Together they lock the cascade in an intermediate state — still active but no longer swinging between peak and trough.
Because the rhythm flattens, Alzheimer’s tissue shows elevated average DREAM activity, which was read as stronger repression of DNA repair. The model argues this reflects a lost oscillation, not deeper suppression. Consequently, drugs with constant release would further blunt the needed swing; a short dose timed to the sleep phase is preferable. Internal time can be measured with the HairTime test, which reads 17 clock genes from a single plucked hair.
The framework aligns with Nedergaard’s findings that sleep‑driven cerebrospinal fluid flow clears amyloid and tau, explaining why lecanemab and donanemab give only modest cognitive gains. If the DNA‑repair clock is broken,
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A theoretical model published 17 September in GeroScience ties together two hallmarks of brain aging: the buildup of DNA damage in neurons and the weakening of circadian rhythms. The authors propose the enzyme tyrosyl‑tRNA synthetase (TyrRS) as a molecular switch that coordinates both processes and explain why they falter together in aging and Alzheimer’s disease.
TyrRS normally charges tyrosine onto tRNA for protein synthesis, but when free tyrosine is low — during the night or fasting — a fraction translocates to the nucleus. There it activates PARP1 to detect DNA breaks, keeps transposable‑element DNA silenced to prevent inflammation, and induces the LIN9 gene. LIN9 joins the DREAM complex, which by day represses 67 DNA‑repair genes (including BRCA1) and releases them at night for repair.
The oscillation amplitude of these three activities matters more than their average level. With age, blood tyrosine rises 15–25%, narrowing the nighttime window for TyrRS action, while suprachiasmatic‑nucleus neuron loss dampens circadian rhythms. Together they lock the cascade in an intermediate state — still active but no longer swinging between peak and trough.
Because the rhythm flattens, Alzheimer’s tissue shows elevated average DREAM activity, which was read as stronger repression of DNA repair. The model argues this reflects a lost oscillation, not deeper suppression. Consequently, drugs with constant release would further blunt the needed swing; a short dose timed to the sleep phase is preferable. Internal time can be measured with the HairTime test, which reads 17 clock genes from a single plucked hair.
The framework aligns with Nedergaard’s findings that sleep‑driven cerebrospinal fluid flow clears amyloid and tau, explaining why lecanemab and donanemab give only modest cognitive gains. If the DNA‑repair clock is broken,
🔗 Read original →
Nature
DREAM repressive activity links somatic mutation, lifespan and disease
Nature Aging - The DREAM complex is a transcriptional repressor of DNA repair. Koch et al. infer DREAM activity via expression of its repressed targets and use DREAM knockout mice to link DREAM...
Mitochondrial Complex I vs IV Damage Extends Worm Life via Distinct Pathways, Metformin Effects Differ
Mahidol University & Ghent University preprint, September 17
Researchers compared the effects of knocking down Complex I (nuo‑6) and Complex IV (cco‑1) in *C. elegans*. Inhibition of Complex I raised median lifespan from 17→19 days, while Complex IV inhibition extended it further to 24 days.
Both knockdowns activated the mitochondrial unfolded‑protein response (UPRmt) via ATFS‑1, but the downstream requirements diverged. Loss of ATFS‑1 collapsed the Complex I benefit to 15 days (below control), whereas Complex IV worms retained a 24‑day median despite lost chaperone production.
The AMPK homolog AAK‑2 showed mirror‑image effects: its removal slightly boosted Complex I longevity to 21 days, but knocked Complex IV lifespan down to about 15 days. Metformin, which inhibits Complex I and activates AAK‑2, added a second hit to Complex I/AAK‑2 worms, dropping median from 21→18 days, yet it markedly prolonged Complex IV worms from 24→30 days and even rescued AAK‑2‑deficient IV worms from 15→20 days.
These findings reconcile earlier contradictory reports: ATFS‑1 was deemed essential for Complex I‑driven longevity in 2018, while 2014 showed Complex IV worms lived long without ATFS‑1. The new work shows both are correct, acting on different respiratory‑chain nodes, and suggests that drugs like metformin must be tested separately for each complex.
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Mahidol University & Ghent University preprint, September 17
Researchers compared the effects of knocking down Complex I (nuo‑6) and Complex IV (cco‑1) in *C. elegans*. Inhibition of Complex I raised median lifespan from 17→19 days, while Complex IV inhibition extended it further to 24 days.
Both knockdowns activated the mitochondrial unfolded‑protein response (UPRmt) via ATFS‑1, but the downstream requirements diverged. Loss of ATFS‑1 collapsed the Complex I benefit to 15 days (below control), whereas Complex IV worms retained a 24‑day median despite lost chaperone production.
The AMPK homolog AAK‑2 showed mirror‑image effects: its removal slightly boosted Complex I longevity to 21 days, but knocked Complex IV lifespan down to about 15 days. Metformin, which inhibits Complex I and activates AAK‑2, added a second hit to Complex I/AAK‑2 worms, dropping median from 21→18 days, yet it markedly prolonged Complex IV worms from 24→30 days and even rescued AAK‑2‑deficient IV worms from 15→20 days.
These findings reconcile earlier contradictory reports: ATFS‑1 was deemed essential for Complex I‑driven longevity in 2018, while 2014 showed Complex IV worms lived long without ATFS‑1. The new work shows both are correct, acting on different respiratory‑chain nodes, and suggests that drugs like metformin must be tested separately for each complex.
🔗 Read original →
bioRxiv
Divergent Retrograde Signaling Pathways Coordinate Longevity and Metformin Responses in Complex I and Complex IV Deficient C. elegans
Mild reductions in mitochondrial electron transport chain (ETC) capacity paradoxically extend organismal lifespan, a conserved phenomenon termed mitohormesis. While the mitochondrial unfolded protein response (UPRmt) and AMP-activated protein kinase (AMPK)…
Frailty Index for House Crickets Shows Rapamycin Reduces Age‑Related Decline
On Sep 17 the lab of geropathologist Warren Ladiges at the University of Washington published a frailty index for the house cricket *Acheta domesticus* in npj Aging, September 17. It is the first quantitative measure of functional aging for this species.
The index combines ten video‑tracked behavioral parameters, each scored 0–4 and summed to a total frailty score from 0 to 1, with higher values indicating greater decline. In young (4–6 weeks) and old (10–12 weeks) crickets the score rose similarly for both sexes, from 0.38 to 0.65 in females and from 0.38 to 0.67 in males.
To test the index, middle‑aged crickets (8 weeks) were fed rapamycin, acarbose or phenylbutyrate for two weeks using doses from the NIA’s Interventions Testing Program. By 10 weeks the frailty index of the rapamycin group had dropped nearly half relative to controls in both sexes, whereas acarbose and phenylbutyrate showed no significant effect.
In humans frailty is a state distinct from chronological age that reflects loss of physiological reserves and predicts risk better than years lived; geriatrics assess it by summing deficits across aging traits. The authors applied the same logic to crickets, creating a tool analogous to a clinical frailty index.
The index is intended as a cheap, fast first screen for geroprotector candidates such as metformin, SGLT2
🔗 Read original →
On Sep 17 the lab of geropathologist Warren Ladiges at the University of Washington published a frailty index for the house cricket *Acheta domesticus* in npj Aging, September 17. It is the first quantitative measure of functional aging for this species.
The index combines ten video‑tracked behavioral parameters, each scored 0–4 and summed to a total frailty score from 0 to 1, with higher values indicating greater decline. In young (4–6 weeks) and old (10–12 weeks) crickets the score rose similarly for both sexes, from 0.38 to 0.65 in females and from 0.38 to 0.67 in males.
To test the index, middle‑aged crickets (8 weeks) were fed rapamycin, acarbose or phenylbutyrate for two weeks using doses from the NIA’s Interventions Testing Program. By 10 weeks the frailty index of the rapamycin group had dropped nearly half relative to controls in both sexes, whereas acarbose and phenylbutyrate showed no significant effect.
In humans frailty is a state distinct from chronological age that reflects loss of physiological reserves and predicts risk better than years lived; geriatrics assess it by summing deficits across aging traits. The authors applied the same logic to crickets, creating a tool analogous to a clinical frailty index.
The index is intended as a cheap, fast first screen for geroprotector candidates such as metformin, SGLT2
🔗 Read original →
Nature
A composite frailty index enables quantification of functional aging and identification of gerotherapeutic drugs in the house cricket
npj Aging - A composite frailty index enables quantification of functional aging and identification of gerotherapeutic drugs in the house cricket
Proteomic map reveals stepwise collapse of protein quality control in human cell senescence
Scientists at the Institute of Molecular Biology in Mainz used mass spectrometry to track how the protein makeup of human IMR90 lung fibroblasts changes across four sequential aging stages of replicative senescence, measuring 5923 proteins per stage. The work was published 16 September in Nature Communications.
They found that nuclear and chromatin proteins are lost first, while DNA‑replication proteins and one histone variant persist longest. About 10% of the changing proteins behave opposite to their RNA levels — accumulating transcripts but disappearing as proteins — a pattern also seen in the brain of the killifish, a model of aging.
The most striking change concerns the cell’s cleanup systems: despite more protein debris, autophagy speed and proteasome
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Scientists at the Institute of Molecular Biology in Mainz used mass spectrometry to track how the protein makeup of human IMR90 lung fibroblasts changes across four sequential aging stages of replicative senescence, measuring 5923 proteins per stage. The work was published 16 September in Nature Communications.
They found that nuclear and chromatin proteins are lost first, while DNA‑replication proteins and one histone variant persist longest. About 10% of the changing proteins behave opposite to their RNA levels — accumulating transcripts but disappearing as proteins — a pattern also seen in the brain of the killifish, a model of aging.
The most striking change concerns the cell’s cleanup systems: despite more protein debris, autophagy speed and proteasome
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Naked mole‑rat microglia hoard fat, shielding the brain from aging
The naked mole‑rat, a mouse‑sized rodent with an almost non‑aging brain and a lifespan of ~40 years, shows almost no typical age‑related diseases such as cancer, cardiovascular illness, or neurodegeneration.
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The naked mole‑rat, a mouse‑sized rodent with an almost non‑aging brain and a lifespan of ~40 years, shows almost no typical age‑related diseases such as cancer, cardiovascular illness, or neurodegeneration.
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Nature
Lipid-droplet-accumulating microglia represent a dysfunctional and proinflammatory state in the aging brain
Nature Neuroscience - Microglia in the aging hippocampus accumulate lipid droplets, and are functionally impaired and inflamed. Lipid droplet formation in microglia is regulated by genes linked to...
Sex differences in immune aging revealed in uncastrated beagles
On 15 September a group from the Southern University of Science and Technology in Shenzhen and co‑authors posted a preprint on bioRxiv. They examined 80 uncastrated laboratory beagles aged 1–11 years and found that age‑related immune remodeling strongly depended on sex.
In both sexes leukocyte numbers declined with age, but in the oldest geriatric subgroup some markers rose again, showing non‑linear blood aging. Cytokine patterns diverged sharply: males showed significant changes in 9 of 40 cytokines (most increasing with age then falling in deep old age), whereas females changed only 2 of the same 40. Similar sex‑dependent shifts appeared for several erythrocytic traits, such as hemoglobin, but not for total leukocyte count.
Dogs share our environment and age‑related diseases while aging faster, making them useful models. However, most companion dogs are neutered, and sex hormones—major regulators of immune cells—mask natural sex differences in those cohorts. By studying uncastrated beagles the authors could observe the underlying divergence.
The classic view of immune aging as a single linear process common to all was contradicted; the data formed two distinct curves depending on sex. In humans, immune aging is also more heritable in men than in women.
To test whether interventions reveal the same sex specificity, the same team treated a separate group of 24 young beagles for 90 days with rapamycin, canagliflozin, or calorie restriction.
Rapamycin produced the broadest response: leukocyte and neutrophil counts rose, while GM‑CSF, IL‑10, MCP‑1 and TNF‑α fell, yet four other cytokines increased, indicating simultaneous suppression and activation of immune signals.
Canagliflozin, chosen because it extended male mouse lifespan by 14% but not female, caused weight loss in males already in the first month and in females
🔗 Read original →
On 15 September a group from the Southern University of Science and Technology in Shenzhen and co‑authors posted a preprint on bioRxiv. They examined 80 uncastrated laboratory beagles aged 1–11 years and found that age‑related immune remodeling strongly depended on sex.
In both sexes leukocyte numbers declined with age, but in the oldest geriatric subgroup some markers rose again, showing non‑linear blood aging. Cytokine patterns diverged sharply: males showed significant changes in 9 of 40 cytokines (most increasing with age then falling in deep old age), whereas females changed only 2 of the same 40. Similar sex‑dependent shifts appeared for several erythrocytic traits, such as hemoglobin, but not for total leukocyte count.
Dogs share our environment and age‑related diseases while aging faster, making them useful models. However, most companion dogs are neutered, and sex hormones—major regulators of immune cells—mask natural sex differences in those cohorts. By studying uncastrated beagles the authors could observe the underlying divergence.
The classic view of immune aging as a single linear process common to all was contradicted; the data formed two distinct curves depending on sex. In humans, immune aging is also more heritable in men than in women.
To test whether interventions reveal the same sex specificity, the same team treated a separate group of 24 young beagles for 90 days with rapamycin, canagliflozin, or calorie restriction.
Rapamycin produced the broadest response: leukocyte and neutrophil counts rose, while GM‑CSF, IL‑10, MCP‑1 and TNF‑α fell, yet four other cytokines increased, indicating simultaneous suppression and activation of immune signals.
Canagliflozin, chosen because it extended male mouse lifespan by 14% but not female, caused weight loss in males already in the first month and in females
🔗 Read original →
bioRxiv
Sex-dimorphic immune trajectories across the canine lifespan and early-life signatures of geroprotective interventions
Canine models are invaluable for translational geroscience, but widespread gonadectomy in companion dogs obscures natural sex-specific aging trajectories. Here, we characterize the age-associated hematologic and serum cytokine profiles of 80 intact laboratory…
Dreaming of a Rationalist-Transhumanist Hearts of Iron 4 Mod
Generally, I dream of a mod for Hearts of Iron 4 built around transforming countries into rationalist-transhumanist societies. It would focus on modeling technological competition.
🔗 Source: @solid_state_humanity
Generally, I dream of a mod for Hearts of Iron 4 built around transforming countries into rationalist-transhumanist societies. It would focus on modeling technological competition.
🔗 Source: @solid_state_humanity
Telegram
Solid State Humanity
Взагалі, я мрію про мод для Hearts of Iron 4, побудований навколо перетворення країн на раціоналістично-трансгуманістичні суспільства і моделювання технологічної конкуренції.
Seven drug targets identified for sarcopenia as first myostatin blocker gains FDA approval
A review published in Nature Reviews Drug Discovery on 7 September 2026 mapped seven pharmacological mechanisms against sarcopenia, the age‑related loss of muscle mass and strength that currently has no approved drugs.
Four days later, on 11 September, the FDA approved apitegromab from Scholar Rock, the first‑ever myostatin‑blocking drug, for spinal muscular atrophy.
In the same week, trial data showed that apitegromab combined with tirzepatide almost halved muscle loss during weight loss, and the EMBRAZE study found the pair preserved 54.9% more muscle mass than tirzepatide alone over 24 weeks.
Sarcopenia is a distinct diagnosis: after age 50 people lose about 10% per decade of muscle, and between 40 and 80 years the loss ranges from one‑third to one‑half. The diagnostic code appeared in 2016 and the clinical definition in 2019, without which there were no insurance coverage or trial criteria.
The review highlights seven independent mechanisms, including declining cellular energy, exhausted stem cells (which drop 24% in women and 37% in men with age, two‑thirds of the remaining cells being poorly functional), loss of nerve‑muscle connections, and vascular inflammation. It also notes the enzyme 15‑PGDH as a “gerozyme” whose inhibition in old mice rejuvenated muscle, intestine, kidney, lung and even memory, and that blocking it restored exercise‑induced muscle growth, boosting strength nearly 50% above untreated animals.
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A review published in Nature Reviews Drug Discovery on 7 September 2026 mapped seven pharmacological mechanisms against sarcopenia, the age‑related loss of muscle mass and strength that currently has no approved drugs.
Four days later, on 11 September, the FDA approved apitegromab from Scholar Rock, the first‑ever myostatin‑blocking drug, for spinal muscular atrophy.
In the same week, trial data showed that apitegromab combined with tirzepatide almost halved muscle loss during weight loss, and the EMBRAZE study found the pair preserved 54.9% more muscle mass than tirzepatide alone over 24 weeks.
Sarcopenia is a distinct diagnosis: after age 50 people lose about 10% per decade of muscle, and between 40 and 80 years the loss ranges from one‑third to one‑half. The diagnostic code appeared in 2016 and the clinical definition in 2019, without which there were no insurance coverage or trial criteria.
The review highlights seven independent mechanisms, including declining cellular energy, exhausted stem cells (which drop 24% in women and 37% in men with age, two‑thirds of the remaining cells being poorly functional), loss of nerve‑muscle connections, and vascular inflammation. It also notes the enzyme 15‑PGDH as a “gerozyme” whose inhibition in old mice rejuvenated muscle, intestine, kidney, lung and even memory, and that blocking it restored exercise‑induced muscle growth, boosting strength nearly 50% above untreated animals.
🔗 Read original →
Nature
Strengthening muscle for healthy ageing: innovative treatments for sarcopenia
Nature Reviews Drug Discovery - There are currently no approved therapies for sarcopenia, the age-related loss of skeletal muscle mass and strength. This Review discusses advances in understanding...
Splice-site disruption extends progeric mouse lifespan 2.4‑fold and restores fertility
On 18 September a preprint from the lab of Zhongjun Zhou at Hong Kong University appeared on bioRxiv, 18 September. The researchers used CRISPR‑Cas9 not to correct the LMNA mutation that causes Hutchinson‑Gilford progeria but to destroy the nearby splice‑site signal that the mutation hyper‑activates.
By cutting the DNA at the splice‑site anchor, the guide RNA preferentially hits the mutant allele and breaks the donor site, which is enough to abolish the aberrant splicing. In patient fibroblasts this reduced progerin production by **92
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On 18 September a preprint from the lab of Zhongjun Zhou at Hong Kong University appeared on bioRxiv, 18 September. The researchers used CRISPR‑Cas9 not to correct the LMNA mutation that causes Hutchinson‑Gilford progeria but to destroy the nearby splice‑site signal that the mutation hyper‑activates.
By cutting the DNA at the splice‑site anchor, the guide RNA preferentially hits the mutant allele and breaks the donor site, which is enough to abolish the aberrant splicing. In patient fibroblasts this reduced progerin production by **92
🔗 Read original →
bioRxiv
Genomic splice-donor disruption rescues systemic disease in progeria
RNA splicing determines which protein isoforms a gene produces, and aberrant splice-site activation can cause severe disease. In Hutchinson–Gilford progeria syndrome, a synonymous LMNA mutation strengthens a cryptic 5' splice donor site to produce progerin…
Longeveron’s stem‑cell therapy fails in infant heart trial, shares plunge
On 16 September Longeveron announced that its cell therapy laromeestrocel did not improve heart function in the phase 2b ELPIS II trial of infants with hypoplastic left heart syndrome. The difference in right‑ventricular ejection fraction after 12 months was –0.7 percentage points, which was not statistically significant.
The news sent the stock down 59% the following day, and it kept falling to close at $2.49 on 18 September, giving the company a market value of about $7.9 million. Longeveron said its cash reserves, reported on 12 August, would last only until the end of the year.
Despite the setback, the company highlighted a 31% reduction in cardiovascular events and a 63.4‑meter gain in a six‑minute walk test from its frailty program, and noted that laromeestrocel remains in the XPRIZE Healthspan finals with a $1 million award. Longeveron is now reviewing strategic options and seeking new investors to keep the frailty program alive.
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On 16 September Longeveron announced that its cell therapy laromeestrocel did not improve heart function in the phase 2b ELPIS II trial of infants with hypoplastic left heart syndrome. The difference in right‑ventricular ejection fraction after 12 months was –0.7 percentage points, which was not statistically significant.
The news sent the stock down 59% the following day, and it kept falling to close at $2.49 on 18 September, giving the company a market value of about $7.9 million. Longeveron said its cash reserves, reported on 12 August, would last only until the end of the year.
Despite the setback, the company highlighted a 31% reduction in cardiovascular events and a 63.4‑meter gain in a six‑minute walk test from its frailty program, and noted that laromeestrocel remains in the XPRIZE Healthspan finals with a $1 million award. Longeveron is now reviewing strategic options and seeking new investors to keep the frailty program alive.
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GlobeNewswire News Room
Longeveron Announces Topline Results from ELPIS II Phase 2b Clinical Trial Evaluating Laromestrocel as a Potential Treatment for…
Longeveron Announces Topline Results from ELPIS II Phase 2b Clinical Trial Evaluating Laromestrocel as a Potential Treatment for HLHS...
ByteDance closed the first external funding round for its AI‑driven drug spin‑off Anew Labs on September 16, 2026, securing $290 million at a $1.5 billion valuation, according to Reuters. The round was led by HSG (formerly
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Karl Pfleger argues aging therapies should be judged by multi‑disease benefit, not lifespan
On 18 September 2026, investor Karl Pfleger responded to Professor João Pedro de Magalhães’ question about how to judge anti‑aging therapies if not by lifespan. Pfleger proposed an alternative criterion and noted that the only organization testing such combinations in practice, the LEV Foundation, ran an experiment where two of three approaches failed and a larger follow‑up remains unfunded due to lack of money.
On 9 August 2026, de Magalhães wrote that humanity is not approaching victory over aging, citing that over the past century the only reliable way to extend mouse lifespan has been caloric restriction. Pfleger replied on 10 August that measuring progress by a single best therapy is mistaken, because aging comprises at least seven distinct molecular breakdowns—such as senescent‑cell accumulation—that require different treatments, just as different cancers need different drugs.
On the same day, de Magalhães disagreed, insisting lifespan remains the only reliable metric; otherwise symptomatic relief could be mistaken for anti‑aging effect. On 7 September Pfleger countered with an analogy to the 1960 Moon landing, arguing that demanding immediate success ignores the needed development time. On 17 September de Magalhães acknowledged the need for combination therapies but asked how to prove they work—or don’t.
The next day Pfleger answered: a therapy validates the “geroscience hypothesis” if it treats, alleviates, or prevents several age‑related diseases at once, even if it does not extend life. Individual interventions may show no effect alone; benefit appears only when combined. He cited the LEV Foundation’s RMR1 experiment on 1,000 mice, which showed a single dose of repair does not last longer than one year. Of the three interventions, two were defective—one “broken,” the other “partially broken.” A second, larger trial with eight interventions still seeks funding.
Pfleger lamented that only one group is testing such combinations, calling it regrettable, and noted that structural incentives discou
🔗 Read original →
On 18 September 2026, investor Karl Pfleger responded to Professor João Pedro de Magalhães’ question about how to judge anti‑aging therapies if not by lifespan. Pfleger proposed an alternative criterion and noted that the only organization testing such combinations in practice, the LEV Foundation, ran an experiment where two of three approaches failed and a larger follow‑up remains unfunded due to lack of money.
On 9 August 2026, de Magalhães wrote that humanity is not approaching victory over aging, citing that over the past century the only reliable way to extend mouse lifespan has been caloric restriction. Pfleger replied on 10 August that measuring progress by a single best therapy is mistaken, because aging comprises at least seven distinct molecular breakdowns—such as senescent‑cell accumulation—that require different treatments, just as different cancers need different drugs.
On the same day, de Magalhães disagreed, insisting lifespan remains the only reliable metric; otherwise symptomatic relief could be mistaken for anti‑aging effect. On 7 September Pfleger countered with an analogy to the 1960 Moon landing, arguing that demanding immediate success ignores the needed development time. On 17 September de Magalhães acknowledged the need for combination therapies but asked how to prove they work—or don’t.
The next day Pfleger answered: a therapy validates the “geroscience hypothesis” if it treats, alleviates, or prevents several age‑related diseases at once, even if it does not extend life. Individual interventions may show no effect alone; benefit appears only when combined. He cited the LEV Foundation’s RMR1 experiment on 1,000 mice, which showed a single dose of repair does not last longer than one year. Of the three interventions, two were defective—one “broken,” the other “partially broken.” A second, larger trial with eight interventions still seeks funding.
Pfleger lamented that only one group is testing such combinations, calling it regrettable, and noted that structural incentives discou
🔗 Read original →
PubMed Central (PMC)
The rodent aging interventions database (RAID): a data visualization tool for all studies reporting rodent lifespan extension
Numerous studies have investigated the effects of various interventions on the lifespans of mice and rats. The design of future rodent lifespan extension experiments might consider experimental parameters used in earlier investigations, but finding ...
Food and anti-parasitic treatment slow epigenetic aging in wild mice
Scientists experimentally tested on wild woodland mice that feeding and anti‑parasite treatment slow the epigenetic clocks that measure aging via DNA methylation marks. A team from Edinburgh and Altos Labs built DNA‑methylation clocks for the woodland mouse and transferred them to a wild population near Edinburgh. In the September 16 version of the study, mice that were simultaneously fed and treated for intestinal parasites showed a significantly slower clock rate than untreated animals of the same chronological age.
Wild animals’ ages are rarely known precisely because they are not caught at birth; body mass, tooth wear or telomere length give only rough estimates or require killing the animal. Epigenetic clocks solve this: with age, methylation changes at specific DNA sites predict age. Sarah Wolf and colleagues first trained the clocks on 74 laboratory woodland mice of known age using 177 such marks. The clocks predicted age with an error of 5.45 days on the training set and 14.64 days on independent validation. This is an order of magnitude more accurate than universal pan‑mammalian clocks trained on 18
🔗 Read original →
Scientists experimentally tested on wild woodland mice that feeding and anti‑parasite treatment slow the epigenetic clocks that measure aging via DNA methylation marks. A team from Edinburgh and Altos Labs built DNA‑methylation clocks for the woodland mouse and transferred them to a wild population near Edinburgh. In the September 16 version of the study, mice that were simultaneously fed and treated for intestinal parasites showed a significantly slower clock rate than untreated animals of the same chronological age.
Wild animals’ ages are rarely known precisely because they are not caught at birth; body mass, tooth wear or telomere length give only rough estimates or require killing the animal. Epigenetic clocks solve this: with age, methylation changes at specific DNA sites predict age. Sarah Wolf and colleagues first trained the clocks on 74 laboratory woodland mice of known age using 177 such marks. The clocks predicted age with an error of 5.45 days on the training set and 14.64 days on independent validation. This is an order of magnitude more accurate than universal pan‑mammalian clocks trained on 18
🔗 Read original →
bioRxiv
Epigenetic Clocks Uncover the Natural History of Ageing in Wild Mice
Environmental stressors are expected to accelerate senescence but demonstrating this requires both a measure of senescence and knowledge of chronological age - data rarely available for most wild animals. Here, we constructed a DNA methylation-based epigenetic…
NUS Reveals PROMETHEUS Pilot Protocol Personalizing Anti‑Aging Supplements by Gerotype
On 18 September Professor Andrea Meyer presented the protocol and eight‑week results of the PROMETHEUS trial at the Academy of Healthy Longevity webinar, National University of Singapore. The study is one of the finalists in the XPRIZE Healthspan competition.
Gerotype combines genomic, epigenetic, microbiome and clinical data to capture uneven organ ageing; it determines both who is enrolled and which supplements each participant receives. Participants aged 50–80 received a uniform base package of sleep, nutrition, whey protein, creatine, counselling and combined physical‑cognitive training.
Supplements were added only when a specific ageing biomarker fell below the 50th percentile for age and sex: urolithin A for low muscle strength, nicotinamide mononucleotide for low endurance, and a multivitamin for weak cognitive performance. At week 4 all measures were repeated and doses were adjusted or supplements changed if there was no response, mirroring clinical drug titration.
Enrollees were drawn from the lower 75% of endurance and NIH Toolbox cognition scores, intentionally excluding the top performers; 20 participants completed the program, with an average age 61. Over 80% adhered to the exercise regimen and took most supplements, and the protocol proved safe.
After eight weeks cognitive scores rose significantly — stronger than expected — muscle strength and mass increased significantly, and visceral fat decreased. Peak oxygen consumption (VO₂) did not change significantly, while the CD4/CD8 T‑cell ratio, a marker of immune ageing, shifted significantly toward the 1.5–2 range.
XPRIZE Healthspan offers a $101 million prize; NUS was named a finalist, while ten other teams received $1 million grants for coordinated trials. Meyer’s team is preparing a 12‑month study with 180 participants that will add omega‑3, vitamin D, zinc and coaching to test whether the pilot effects scale up.
In parallel, Meyer and co‑author Ukhvat are designing a trial frameworks that adapt interventions in real time using hierarchical outcomes, responding to new measurements as they arise.
🔗 Read original →
On 18 September Professor Andrea Meyer presented the protocol and eight‑week results of the PROMETHEUS trial at the Academy of Healthy Longevity webinar, National University of Singapore. The study is one of the finalists in the XPRIZE Healthspan competition.
Gerotype combines genomic, epigenetic, microbiome and clinical data to capture uneven organ ageing; it determines both who is enrolled and which supplements each participant receives. Participants aged 50–80 received a uniform base package of sleep, nutrition, whey protein, creatine, counselling and combined physical‑cognitive training.
Supplements were added only when a specific ageing biomarker fell below the 50th percentile for age and sex: urolithin A for low muscle strength, nicotinamide mononucleotide for low endurance, and a multivitamin for weak cognitive performance. At week 4 all measures were repeated and doses were adjusted or supplements changed if there was no response, mirroring clinical drug titration.
Enrollees were drawn from the lower 75% of endurance and NIH Toolbox cognition scores, intentionally excluding the top performers; 20 participants completed the program, with an average age 61. Over 80% adhered to the exercise regimen and took most supplements, and the protocol proved safe.
After eight weeks cognitive scores rose significantly — stronger than expected — muscle strength and mass increased significantly, and visceral fat decreased. Peak oxygen consumption (VO₂) did not change significantly, while the CD4/CD8 T‑cell ratio, a marker of immune ageing, shifted significantly toward the 1.5–2 range.
XPRIZE Healthspan offers a $101 million prize; NUS was named a finalist, while ten other teams received $1 million grants for coordinated trials. Meyer’s team is preparing a 12‑month study with 180 participants that will add omega‑3, vitamin D, zinc and coaching to test whether the pilot effects scale up.
In parallel, Meyer and co‑author Ukhvat are designing a trial frameworks that adapt interventions in real time using hierarchical outcomes, responding to new measurements as they arise.
🔗 Read original →
Nature
The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in…
Nature Metabolism - Here the authors report the results of a first-in-human trial with urolithin A in healthy elderly individuals, demonstrating that the compound is well tolerated and bioavailable...
Virtual Biotech AI Agents Predict Lung Cancer Target, Later Confirmed by FDA Breakthrough Therapy
A virtual biotech company composed of tens of thousands of AI agents analyzed lung‑cancer data available only up to January 2025 and identified the protein B7‑H3 as a therapeutic target, proposing a strategy against it without seeing newer data.
In August 2025, the antibody ifinatamab deruxtecan from Daiichi Sankyo and Merck received FDA breakthrough‑therapy status for the same target, showing a 48% response rate in patients with small‑cell lung cancer.
The work was peer‑reviewed and published on Science, September 17 2026; an analysis of 566 patients revealed that high B7‑H3 activity correlates with a 62% higher risk of death compared to low activity, and spatial mapping showed B7‑H3 accumulating in cancer‑associated fibroblasts that push immune cells out of the tumor microenvironment.
Because no druggable pocket was found on B7‑H3, the team suggested an antibody‑drug conjugate to deliver toxin directly to B7‑H3‑positive cells; Virtual Biotech grew from the earlier Virtual Lab system that had produced COVID nanobodies outperforming human ones, and its agents now read papers and databases directly through the shared Paperclip filesystem.
In a second case, the MOONGLOW trial of vixarelimab for ulcerative colitis was re‑examined; agents found that non‑responders had elevated OSMRβ in fibroblasts before therapy, recommending patient selection based on fibroblast OSMR levels, and noted that Virtual Biotech’s fibroblast‑focused targets are 48% more likely to reach market than broadly active targets.
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A virtual biotech company composed of tens of thousands of AI agents analyzed lung‑cancer data available only up to January 2025 and identified the protein B7‑H3 as a therapeutic target, proposing a strategy against it without seeing newer data.
In August 2025, the antibody ifinatamab deruxtecan from Daiichi Sankyo and Merck received FDA breakthrough‑therapy status for the same target, showing a 48% response rate in patients with small‑cell lung cancer.
The work was peer‑reviewed and published on Science, September 17 2026; an analysis of 566 patients revealed that high B7‑H3 activity correlates with a 62% higher risk of death compared to low activity, and spatial mapping showed B7‑H3 accumulating in cancer‑associated fibroblasts that push immune cells out of the tumor microenvironment.
Because no druggable pocket was found on B7‑H3, the team suggested an antibody‑drug conjugate to deliver toxin directly to B7‑H3‑positive cells; Virtual Biotech grew from the earlier Virtual Lab system that had produced COVID nanobodies outperforming human ones, and its agents now read papers and databases directly through the shared Paperclip filesystem.
In a second case, the MOONGLOW trial of vixarelimab for ulcerative colitis was re‑examined; agents found that non‑responders had elevated OSMRβ in fibroblasts before therapy, recommending patient selection based on fibroblast OSMR levels, and noted that Virtual Biotech’s fibroblast‑focused targets are 48% more likely to reach market than broadly active targets.
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Antimicrobial K21 extends worm lifespan via macrophage mitophagy
K21 is a synthetic antimicrobial compound sold under the brand FiteBac and has been incorporated into FDA‑approved dental products for over ten years. It is used to treat burns and diabetic wounds, shows broad‑spectrum activity against bacteria, viruses and fungi, and does not damage membranes or harm human cells. Researchers hypothesized that its wound‑healing benefits arise from enhanced macrophage activity.
When human macrophages were treated with K21 and infected with the intracellular pathogen Enterococcus faecalis, bacterial uptake remained unchanged but intracellular survival dropped dramatically. The study was published 17 September in Life Science Alliance. Single‑cell RNA sequencing revealed that K21 stimulates mitochondrial fission and subsequent mitophagy by stabilizing the DRP‑1 protein, independent of oxygen deprivation or membrane damage — a process the authors term mitohormesis. In contrast, smokers with a SIRT3 defect in alveolar macrophages show impaired mitophagy and reduced bacterial clearance.
Feeding Caenorhabditis elegans bacteria expressing K21 induced the same mitochondrial fission/mitophagy in the worm intestine and significantly extended lifespan compared with controls (p<0.0001). No changes were observed in feeding, development, body size or egg count, ruling out caloric restriction. Although mitophagy‑mediated lifespan extension in C. elegans is usually linked to the atfs‑1 gene, K21 prolonged life in atfs‑1 mutants, indicating a distinct pathway. Eight genes showed concordant regulation in humans and worms, providing molecular evidence of a conserved mechanism.
The authors conclude that K21’s enhancement of human macrophage antimicrobial defense and its lifespan‑extending effect in worms stem from a single intervention in mitochondrial quality control, linking infection resistance and longevity. Lifespan was measured only in worms; in humans the assay focused on macrophage antimicrobial activity. Both project leaders received grants from FiteBac, which markets K21. K21 remains principally a topical antimicrobial; the mitophagy activity and worm lifespan extension represent newly discovered properties.
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K21 is a synthetic antimicrobial compound sold under the brand FiteBac and has been incorporated into FDA‑approved dental products for over ten years. It is used to treat burns and diabetic wounds, shows broad‑spectrum activity against bacteria, viruses and fungi, and does not damage membranes or harm human cells. Researchers hypothesized that its wound‑healing benefits arise from enhanced macrophage activity.
When human macrophages were treated with K21 and infected with the intracellular pathogen Enterococcus faecalis, bacterial uptake remained unchanged but intracellular survival dropped dramatically. The study was published 17 September in Life Science Alliance. Single‑cell RNA sequencing revealed that K21 stimulates mitochondrial fission and subsequent mitophagy by stabilizing the DRP‑1 protein, independent of oxygen deprivation or membrane damage — a process the authors term mitohormesis. In contrast, smokers with a SIRT3 defect in alveolar macrophages show impaired mitophagy and reduced bacterial clearance.
Feeding Caenorhabditis elegans bacteria expressing K21 induced the same mitochondrial fission/mitophagy in the worm intestine and significantly extended lifespan compared with controls (p<0.0001). No changes were observed in feeding, development, body size or egg count, ruling out caloric restriction. Although mitophagy‑mediated lifespan extension in C. elegans is usually linked to the atfs‑1 gene, K21 prolonged life in atfs‑1 mutants, indicating a distinct pathway. Eight genes showed concordant regulation in humans and worms, providing molecular evidence of a conserved mechanism.
The authors conclude that K21’s enhancement of human macrophage antimicrobial defense and its lifespan‑extending effect in worms stem from a single intervention in mitochondrial quality control, linking infection resistance and longevity. Lifespan was measured only in worms; in humans the assay focused on macrophage antimicrobial activity. Both project leaders received grants from FiteBac, which markets K21. K21 remains principally a topical antimicrobial; the mitophagy activity and worm lifespan extension represent newly discovered properties.
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PubMed Central (PMC)
Inhibition of DRP1-dependent mitochondrial fission by Mdivi-1 alleviates atherosclerosis through the modulation of M1 polarization
Inflammation and immune dysfunction with classically activated macrophages(M1) infiltration are important mechanisms in the progression of atherosclerosis (AS). Dynamin-related protein 1 (DRP1)-dependent mitochondrial fission is a novel target for ...
DNA methylation variability adds independent aging signal boosting mortality prediction
Researchers from Simon Fraser University, the US National Institute on Aging, and Dalhousie University examined DNA methylation in blood from 1445 Canadians aged 45–85. Besides the usual sites where average methylation shifts with health, they searched for loci where the spread of methylation between people of the same age changes, discovering a largely non‑overlapping set of regions.
A biomarker built from both the average level and the variability predicted all‑cause mortality more accurately than either signal alone and outperformed the Horvath, Hannum, and GrimAge clocks in two independent cohorts. The study appeared September 17 in Journal of Gerontology: Series A.
The concept grew from the team’s 2024 work showing that many physiological traits are linked to an optimal middle value, with deviation in either direction worsening health. Similar patterns had been noted for telomere length variability in healthy centenarians and for rising methylation variability in tumours, indicating a loss of epigenetic stability.
Combining 789 CpG sites into a composite score, the biomarker surpassed each individual signal and five established tools—frailty index, Horvath, Hannum, PhenoAge, and GrimAge v2—in a hold‑out Canadian sample, where none of those tools showed a significant mortality link. Its heritability ≈41% indicates that lifestyle and environment drive most of the variation.
The same advantage held in the independent Baltimore Aging Study (728 participants); the biomarker correlated with smoking and inflammation markers such as C‑reactive protein and interleukin‑6. Among five age‑related diseases tested, it significantly predicted only higher risk of chronic obstructive pulmonary disease after a stricter significance threshold to guard against false positives.
A comparable finding emerged recently from the Generation Scotland cohort, where sites showing age‑related increases in methylation variability alone forecast mortality. While epigenetic clocks have traditionally read methylation on a single axis—average level—this work reveals a second, independent axis—variability—and shows that ignoring it incurs a measurable loss in predictive precision.
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Researchers from Simon Fraser University, the US National Institute on Aging, and Dalhousie University examined DNA methylation in blood from 1445 Canadians aged 45–85. Besides the usual sites where average methylation shifts with health, they searched for loci where the spread of methylation between people of the same age changes, discovering a largely non‑overlapping set of regions.
A biomarker built from both the average level and the variability predicted all‑cause mortality more accurately than either signal alone and outperformed the Horvath, Hannum, and GrimAge clocks in two independent cohorts. The study appeared September 17 in Journal of Gerontology: Series A.
The concept grew from the team’s 2024 work showing that many physiological traits are linked to an optimal middle value, with deviation in either direction worsening health. Similar patterns had been noted for telomere length variability in healthy centenarians and for rising methylation variability in tumours, indicating a loss of epigenetic stability.
Combining 789 CpG sites into a composite score, the biomarker surpassed each individual signal and five established tools—frailty index, Horvath, Hannum, PhenoAge, and GrimAge v2—in a hold‑out Canadian sample, where none of those tools showed a significant mortality link. Its heritability ≈41% indicates that lifestyle and environment drive most of the variation.
The same advantage held in the independent Baltimore Aging Study (728 participants); the biomarker correlated with smoking and inflammation markers such as C‑reactive protein and interleukin‑6. Among five age‑related diseases tested, it significantly predicted only higher risk of chronic obstructive pulmonary disease after a stricter significance threshold to guard against false positives.
A comparable finding emerged recently from the Generation Scotland cohort, where sites showing age‑related increases in methylation variability alone forecast mortality. While epigenetic clocks have traditionally read methylation on a single axis—average level—this work reveals a second, independent axis—variability—and shows that ignoring it incurs a measurable loss in predictive precision.
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OUP Academic
DNA methylation variability provides a complementary epigenetic signature of aging heterogeneity: Findings from the Canadian Longitudinal…
AbstractBACKGROUND. Human aging does not follow a single trajectory. Epigenetic changes offer insight into the heterogeneity in aging by reflecting the com
Stanford shows fore‑ and hindbrain arise from distinct progenitor cells
Researchers from Stanford Medicine, Caltech, and UCSF tracked hundreds of progenitor cells in mouse embryos, finding that descendants stayed almost exclusively in either the fore‑/midbrain or the hindbrain stream. Of the 494 clones examined in 16 embryos, mixing between the two streams was virtually absent.
At the 7.5‑day stage, the genes Otx2 and Gbx2 become active in different zones of the neural tube. Labeling cells with active Gbx2 using a short 12‑hour pulse showed that their progeny contributed only to the hindbrain, without mixing with Otx2‑lineage cells.
Attempts to reverse progenitor fate with signaling cues failed, both alone and in combined culture. Chromatin analysis revealed that the two cell types already had distinct DNA accessibility patterns by the 2‑day stage, locking in their developmental programs.
Using the newly identified hindbrain progenitor, the team generated human hindbrain motor neurons that release acetylcholine and fire action potentials. In the body, these neurons control facial, tongue, and throat muscles for swallowing, speech, facial expression, and eye movements.
Loss of such neurons is likely to impair swallowing in spinal muscular atrophy and amyotrophic lateral sclerosis, leading to choking, pneumonia, and sometimes death. The same developmental split helps explain diffuse pontine glioma—the leading cause of cancer death in children, with a five‑year survival of about 1%. Co‑author Michelle Monje received the Brain Prize in 2025 for discovering that healthy neurons form synapses with glioma cells and electrically stimulate their growth.
The progenitor
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Researchers from Stanford Medicine, Caltech, and UCSF tracked hundreds of progenitor cells in mouse embryos, finding that descendants stayed almost exclusively in either the fore‑/midbrain or the hindbrain stream. Of the 494 clones examined in 16 embryos, mixing between the two streams was virtually absent.
At the 7.5‑day stage, the genes Otx2 and Gbx2 become active in different zones of the neural tube. Labeling cells with active Gbx2 using a short 12‑hour pulse showed that their progeny contributed only to the hindbrain, without mixing with Otx2‑lineage cells.
Attempts to reverse progenitor fate with signaling cues failed, both alone and in combined culture. Chromatin analysis revealed that the two cell types already had distinct DNA accessibility patterns by the 2‑day stage, locking in their developmental programs.
Using the newly identified hindbrain progenitor, the team generated human hindbrain motor neurons that release acetylcholine and fire action potentials. In the body, these neurons control facial, tongue, and throat muscles for swallowing, speech, facial expression, and eye movements.
Loss of such neurons is likely to impair swallowing in spinal muscular atrophy and amyotrophic lateral sclerosis, leading to choking, pneumonia, and sometimes death. The same developmental split helps explain diffuse pontine glioma—the leading cause of cancer death in children, with a five‑year survival of about 1%. Co‑author Michelle Monje received the Brain Prize in 2025 for discovering that healthy neurons form synapses with glioma cells and electrically stimulate their growth.
The progenitor
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Nature
A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer
Nature - A role for Gbx2 in repression of Otx2 and positioning the mid/hindbrain organizer
Scientists Reverse APOE4‑Driven Blood‑Brain Barrier Leak by Targeting Fibronectin
Although the APOE4 variant has recently been linked to longevity, it also triggers a dangerous side‑mechanism that scientists have now deciphered and learned to reverse. In Alzheimer’s disease the blood‑brain barrier becomes leaky because of pathological accumulation of the protein fibronectin. Normally fibronectin acts as a “scaffold” for wound healing, but under the influence of APOE4, inflammation and amyloid plaques astrocytes overproduce it.
Excess fibronectin clogs blood vessels, blocks chemical signals (including VEGF receptors) and destroys tight‑junction contacts, letting blood
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Although the APOE4 variant has recently been linked to longevity, it also triggers a dangerous side‑mechanism that scientists have now deciphered and learned to reverse. In Alzheimer’s disease the blood‑brain barrier becomes leaky because of pathological accumulation of the protein fibronectin. Normally fibronectin acts as a “scaffold” for wound healing, but under the influence of APOE4, inflammation and amyloid plaques astrocytes overproduce it.
Excess fibronectin clogs blood vessels, blocks chemical signals (including VEGF receptors) and destroys tight‑junction contacts, letting blood
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Nature
Fibronectin mediates APOE4-driven blood–brain barrier dysfunction in Alzheimer’s disease
Nature Aging - Bhattarai, Yilmaz and colleagues identify astrocyte-derived fibronectin as a key driver of blood–brain barrier dysfunction in Alzheimer’s disease, linking APOE ε4...
Anthropic Confirms Own Wet Lab for Claude‑Driven Robot Experiments
On 18 September 2026, Eric Cauderer‑Abrams, head of Anthropic’s life sciences division, told Reuters that the company owns and operates its own “wet” laboratory in the San Francisco Bay area. The facility lets Claude direct robots to run experiments with minimal human involvement, though a human operator remains required for safety. A company spokesperson said the lab focuses on fundamental biology, not drug development.
Previously Anthropic was known mainly for providing tools to external labs; in April it bought startup Coefficient Bio for $400 million in stock. In June it launched Claude Science, a workbench for researchers, and announced preclinical programs for diseases that are not profitable for pharma. In August Claude designed 1320 mini‑proteins for 15 targets, and two external contract labs verified the binding while Anthropic itself did not touch the test tubes.
Also in August Anthropic opened the Model Hardware Standard, letting AI agents remotely read and adjust external instruments; in one
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On 18 September 2026, Eric Cauderer‑Abrams, head of Anthropic’s life sciences division, told Reuters that the company owns and operates its own “wet” laboratory in the San Francisco Bay area. The facility lets Claude direct robots to run experiments with minimal human involvement, though a human operator remains required for safety. A company spokesperson said the lab focuses on fundamental biology, not drug development.
Previously Anthropic was known mainly for providing tools to external labs; in April it bought startup Coefficient Bio for $400 million in stock. In June it launched Claude Science, a workbench for researchers, and announced preclinical programs for diseases that are not profitable for pharma. In August Claude designed 1320 mini‑proteins for 15 targets, and two external contract labs verified the binding while Anthropic itself did not touch the test tubes.
Also in August Anthropic opened the Model Hardware Standard, letting AI agents remotely read and adjust external instruments; in one
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Scientific American
Autonomous labs are running science experiments 24/7
Robots and AI are running experiments around the clock, from battery chemistry to cancer therapies. But can they be trusted to get it right?