As we age, our bodies gradually lose their ability to repair and regenerate. Stem cells diminish, making it increasingly difficult for tissues to heal and maintain balance. This reduction in stem cells is a hallmark of aging and a key driver of age-related diseases. Scientists have long debated whether this decline is the root cause of aging or a side effect. Efforts to use stem cell transplants to reverse aging have faced many challenges, such as ensuring the cells survive and integrate into the body without causing serious side effects, like tumors.
In a recent study published in Cell, researchers from the Chinese Academy of Sciences and Capital Medical University introduced a new type of human stem cell called senescence-resistant mesenchymal progenitor cells (SRCs) by reprogramming the genetic pathways associated with longevity. These cells, which resist aging and stress without developing tumors, were tested on elderly crab-eating macaques, which share physiological similarities with humans in their 60s and 70s.
The research team conducted a 44-week experiment on these macaques. The macaques received biweekly intravenous injections of SRCs, with a dosage of 2×106 cells per kilogram of body weight. The researchers found no adverse effects among the macaques. Detailed assessments confirmed that the transplanted cells did not cause tissue damage or tumors.
The researchers discovered that SRCs triggered a multi-system rejuvenation, reversing key markers of aging across 10 major physiological systems and 61 different tissue types. The treated macaques exhibited improved cognitive function, and tissue analyses indicated a reduction in age-related degenerative conditions such as brain atrophy, osteoporosis, fibrosis, and lipid buildup. 👍
We developed a robust epigenetic clock to estimate age from two wild polar bear subpopulations using blood samples. There was a correlation between epigenetic (DNAm) and chronological age throughout the polar bear lifespan. Polar bears in the wild have a lifespan of approximately 25 years (Rode and Stirling 2018), thus the clock estimates age to ±3% of the polar bear lifespan, although we caution that age estimates may be less accurate for older individuals. Advantages to this method include obtaining more accurate age estimates compared to cementum annuli-derived ages and leveraging samples likely already routinely collected (e.g., blood, tissue) during capture, as opposed to pulling teeth. Further, archived samples or previously extracted DNA may be used for DNAm analysis, extending the value of existing samples and saving money on DNA extraction costs. Our results complement other polar bear clocks (Newediuk et al. 2024, 2025) and provide additional support for the use of DNAm methods to estimate the age of wild mammals (De Paoli-Iseppi et al. 2017).
Our DNAm method estimates polar bear age with a MAE of 0.75 years. In contrast, accuracy of cementum annuli for aging polar bears to within 1 year of actual age has ranged from 32% to 75% (Calvert and Ramsay 1998 ; Christensen-Dalsgaard et al. 2010 ; Hensel and Sorensen 1980). Cementum annuli age estimates are less accurate when made by less experienced observers (Christensen-Dalsgaard et al. 2010 ; Hensel and Sorensen 1980 ; McLaughlin et al. 1990) and can vary between laboratories by 10 years (Christensen-Dalsgaard et al. 2010). For example, in one lab, multiple female polar bears were aged at ~10 years, while a second laboratory aged them at 20 years old (Christensen-Dalsgaard et al. 2010). Our method removes these sources of error. We do, however, acknowledge a potential source of technical error, given that all but three of the tooth-aged samples were run on one plate, and the majority of our known age samples were run on another plate.
The ER-100 drug candidate reverses aging in mice, and David Sinclair says human trials start soon. Is this a magic pill for aging? Dr. Aubrey de Grey discusses the latest advances in life-extension research.
Our story begins on X, where user “rand_longevity” wrote, “Aging will be reversible in humans within 8 years”, to which Dr. David Sinclair replied, “8 years? After successful non-human primate trials, human age reversal trials are set to begin in 6 months”, later naming the ER-100 drug candidate.
Life Biosciences ER-100 drug candidate leverages partial epigenetic programming using 3 of the 4 Yamanaka factors to promote cellular rejuvenation to a younger state without the loss of cell identity. They believe this will help prevent or reverse age-related diseases at a root level — but they’re not the only organization pursuing life-extension research.
Dr. de Grey’s own research has focused primarily on accumulated side effects from metabolism, embodied in the title of his 1999 book, “The Mitochondrial Free Radical Theory of Aging”.
Dr. de Grey is well-known as one of the top gerontology and life-extension scientists in the world, and his own work has also been successful in extending the lifespan of lab animals. In this program, he discusses his work and some of the key elements of living a longer, healthier life.
DISCLAIMER: This program is a discussion is about ongoing scientific research, and is NOT providing medical advice. Please consult your doctor before starting any supplements, beginning an exercise routine, or undertaking lifestyle changes.
A clinical study shows that pterostilbene, a natural compound, significantly improves signs of aging in the skin, pointing to a new direction in skincare science. As interest in anti-aging skincare continues to surge, scientists in China have conducted a clinical trial to test the effectiveness o
We present EpInflammAge, an explainable deep learning tool that integrates epigenetic and inflammatory markers to create a highly accurate, disease-sensitive biological age predictor. This novel approach bridges two key hallmarks of aging—epigenetic alterations and immunosenescence. First, epigenetic and inflammatory data from the same participants was used for AI models predicting levels of 24 cytokines from blood DNA methylation. Second, open-source epigenetic data (25 thousand samples) was used for generating synthetic inflammatory biomarkers and training an age estimation model. Using state-of-the-art deep neural networks optimized for tabular data analysis, EpInflammAge achieves competitive performance metrics against 34 epigenetic clock models, including an overall mean absolute error of 7 years and a Pearson correlation coefficient of 0.85 in healthy controls, while demonstrating robust sensitivity across multiple disease categories. Explainable AI revealed the contribution of each feature to the age prediction. The sensitivity to multiple diseases due to combining inflammatory and epigenetic profiles is promising for both research and clinical applications. EpInflammAge is released as an easy-to-use web tool that generates the age estimates and levels of inflammatory parameters for methylation data, with the detailed report on the contribution of input variables to the model output for each sample.
Scientists at Columbia Engineering have developed an injectable hydrogel made from yogurt-derived extracellular vesicles (EVs) that could revolutionize regenerative medicine. These EVs serve both as healing agents and as structural components, eliminating the need for added chemicals. The innovation leverages everyday dairy products like yogurt to create a biocompatible material that mimics natural tissue and enhances healing.
A multi-institutional team led by the Chinese Academy of Sciences has constructed a proteomic atlas of human aging across 13 organs, revealing tissue-specific aging clocks, transcriptome-proteome decoupling, and secreted proteins that may accelerate systemic decline.
Organ-specific aging and deterioration drive vulnerability to chronic diseases. Previous studies focused primarily on plasma proteins or DNA methylation profiles. No investigation has systematically mapped how protein quality control deteriorates differently across tissues identified organ‑specific biological age biomarkers.
In the study, “Comprehensive human proteome profiles across a 50-year lifespan reveal aging trajectories and signatures,” published in Cell, researchers designed a multi-tissue proteomic analysis, charting organ-level protein dynamics and aging-related biomarkers across five decades of adult life to construct a longitudinal proteomic atlas of human aging.
Watch a longevity expert and cryonics expert make the case for their approach to life extension. Emil Kendziorra and Karl Pfleger debate longevity escape velocity timelines, which approach would have greater return from research funding, and more at this live debate from the Biostasis Conference at Vitalist Bay.
