Close-up photo of a mouse's healing skin wound, illustrating hair follicle stem cells switching to repair mode due to low serine levels, as found in a Rockefeller University study.
Close-up photo of a mouse's healing skin wound, illustrating hair follicle stem cells switching to repair mode due to low serine levels, as found in a Rockefeller University study.
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Low serine levels push hair follicle stem cells to repair skin, study finds

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Rockefeller University scientists report that, in mice, hair follicle stem cells switch from fueling hair growth to repairing wounds when the amino acid serine is scarce — a shift governed by the integrated stress response. The peer‑reviewed findings in Cell Metabolism suggest dietary or drug strategies could eventually help speed wound healing.

Researchers have long held that adult skin relies on two main stem‑cell pools: epidermal stem cells to maintain the barrier and hair follicle stem cells (HFSCs) to regenerate hair. The new work shows HFSCs can pivot under stress, rerouting effort from hair growth to wound repair when serine levels drop — a cue that activates the integrated stress response (ISR). Serine is a non‑essential amino acid found in foods such as meat, grains, and milk. (sciencedaily.com)

The study, “The integrated stress response fine‑tunes stem cell fate decisions upon serine deprivation and tissue injury,” was published online June 12, 2025, and appears in the August 5, 2025 print issue of Cell Metabolism (37:8, pp. 1715–1731.e11; DOI: 10.1016/j.cmet.2025.05.010). (pubmed.ncbi.nlm.nih.gov)

Working in mice, the team either removed serine from the diet or blocked HFSCs’ ability to synthesize it. Low serine slowed entry into the hair cycle; when combined with skin injury, ISR activity rose further, suppressing hair growth and prioritizing re‑epithelialization. “Serine deprivation triggers a highly sensitive cellular ‘dial’ that fine tunes the cell’s fate — towards skin and away from hair,” said first author Jesse Novak, an MD‑PhD student in Weill Cornell’s Tri‑Institutional MD‑PhD Program and former Ph.D. student in Elaine Fuchs’s lab. (pubmed.ncbi.nlm.nih.gov)

“Most skin wounds that we get are from abrasions, which destroy the upper part of the skin,” Novak said. “That area is home to a pool of stem cells that normally takes charge in wound repair. But when these cells are destroyed, it forces hair follicle stem cells to take the lead.” (rockefeller.edu)

The authors note that earlier work from the Fuchs lab linked dietary serine restriction to curbing precancerous skin cells, prompting trials that explore serine‑limited diets in oncology. The current study examines how serine scarcity reshapes regeneration in healthy tissues. (rockefeller.edu)

Despite that influence, the body tightly regulates circulating serine: feeding mice six times the usual dietary serine raised levels by only about 50%. Even so, in HFSCs unable to make their own serine, a high‑serine diet partially restored hair regeneration. (sciencedaily.com)

“No one likes to lose hair, but when it comes down to survival in stressful times, repairing the epidermis takes precedence,” Fuchs said, adding that the group will test whether lowering serine intake or using ISR‑targeting drugs can accelerate wound closure, and whether other amino acids have similar effects. (sciencedaily.com)

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Scientist in lab studying wound healing process with skin cells and SerpinB3 protein visualization.
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ASU-led study finds cancer marker SerpinB3 also drives wound healing

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Researchers at Arizona State University report that SerpinB3 — a protein better known as a cancer biomarker — plays a natural role in wound repair by spurring skin cells to migrate and rebuild tissue. The peer‑reviewed study appears in Proceedings of the National Academy of Sciences.

Japanese researchers report that hair graying and melanoma can arise from the same melanocyte stem cells, which take different paths depending on DNA damage and local signals. Published online October 6, 2025 in Nature Cell Biology, the University of Tokyo-led study outlines a protective differentiation program that promotes graying and how carcinogens can subvert it to favor melanoma.

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Researchers at UCLA have identified a protein that slows muscle repair in aging but enhances cell survival in mice. Blocking the protein improved healing speed in older mice, though it reduced long-term stem cell resilience. The findings suggest aging involves survival strategies rather than mere decline.

Researchers at The Rockefeller University have identified a molecular switch in breast cancer cells that helps them survive harsh conditions. The switch involves deacetylation of the MED1 protein, which boosts stress-response gene activity linked to tumor growth and resilience. The work, reported in Nature Chemical Biology, points to potential new targets for cancer therapy.

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Researchers have discovered why polyamines, compounds promoted for anti-aging benefits, may also promote cancer growth. The study shows that these molecules activate different proteins in healthy versus cancerous cells, leading to contrasting effects. Led by experts at Tokyo University of Science, the findings were published in the Journal of Biological Chemistry.

Researchers at the University of Victoria have discovered that the protein Reelin could help repair leaky gut caused by chronic stress and alleviate depression symptoms. A single injection restored Reelin levels in preclinical models, showing antidepressant effects. The findings highlight the gut-brain connection in mental health.

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Researchers in France have found that hormone‑sensitive lipase (HSL), long known for breaking down stored fat, also operates in the nucleus of fat cells to help maintain adipose tissue health. When HSL is missing, fat tissue in mice shrinks instead of expanding, leading to lipodystrophy, a finding that helps explain shared health risks between obesity and fat‑loss disorders.

 

 

 

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