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对抗与年龄相关的 VEGF 信号不足可促进健康衰老并延长寿命。

Counteracting age-related VEGF signaling insufficiency promotes healthy aging and extends life span.

机构信息

Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

Wohl Institute for Translational Medicine and the Goldyne Savad Institute for Gene Therapy, Hadassah Hospital, Jerusalem, Israel.

出版信息

Science. 2021 Jul 30;373(6554). doi: 10.1126/science.abc8479.

Abstract

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.

摘要

衰老是血管疾病的既定风险因素,但血管老化本身可能导致器官功能的进行性恶化。在这里,我们在老年小鼠中表明,血管内皮生长因子 (VEGF) 信号不足可能是由于诱饵受体产生增加所致,这种不足可能会驱动多个器官系统的生理衰老。增加 VEGF 信号可以防止与年龄相关的毛细血管损失,改善器官灌注和功能,并延长寿命。更健康的衰老表现在代谢和身体成分的改善,以及与衰老相关的病理的改善,包括肝脂肪变性、肌肉减少症、骨质疏松症、“炎症老化”(与年龄相关的多器官慢性炎症)和肿瘤负担增加。这些结果表明,VEGF 信号不足会影响小鼠的器官衰老,并表明调节该途径可能会导致哺乳动物寿命的延长和整体健康状况的改善。

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