寿命
血管内皮生长因子受体
医学
生物
内科学
老年学
生理学
作者
Myriam Grunewald,Saran Kumar,Husni Sharife,E. Volinsky,Alex Gileles‐Hillel,Tamar Licht,Anna Permyakova,Liad Hinden,Shahar Azar,Yasmin Friedmann,P. Kupetz,R. Tzuberi,Andrey Anisimov,Kari Alitalo,M. J. Horwitz,Shira Leebhoff,Oleksiy-Zakhar Khoma,Ruslan Hlushchuk,Valentin Djonov,Rinat Abramovitch,Joseph Tam,Eli Keshet
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-07-29
卷期号:373 (6554)
被引量:180
标识
DOI:10.1126/science.abc8479
摘要
Aging is an established risk factor for vascular diseases, but vascular aging itself may contribute to the progressive deterioration of organ function. Here, we show in aged mice that vascular endothelial growth factor (VEGF) signaling insufficiency, which is caused by increased production of decoy receptors, may drive physiological aging across multiple organ systems. Increasing VEGF signaling prevented age-associated capillary loss, improved organ perfusion and function, and extended life span. Healthier aging was evidenced by favorable metabolism and body composition and amelioration of aging-associated pathologies including hepatic steatosis, sarcopenia, osteoporosis, "inflammaging" (age-related multiorgan chronic inflammation), and increased tumor burden. These results indicate that VEGF signaling insufficiency affects organ aging in mice and suggest that modulating this pathway may result in increased mammalian life span and improved overall health.
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