دورية أكاديمية

Endothelial cell‐specific reduction in mTOR ameliorates age‐related arterial and metabolic dysfunction.

التفاصيل البيبلوغرافية
العنوان: Endothelial cell‐specific reduction in mTOR ameliorates age‐related arterial and metabolic dysfunction.
المؤلفون: Islam, Md Torikul, Hall, Shelby A., Dutson, Tavia, Bloom, Samuel I., Bramwell, R. Colton, Kim, John, Tucker, Jordan R., Machin, Daniel R., Donato, Anthony J., Lesniewski, Lisa A.
المصدر: Aging Cell; Feb2024, Vol. 23 Issue 2, p1-12, 12p
مصطلحات موضوعية: PANCREATIC beta cells, METABOLIC disorders, VASCULAR smooth muscle, MTOR protein, CELLULAR aging, VASCULAR endothelium, OLD age
مستخلص: Systemic inhibition of the mammalian target of rapamycin (mTOR) delays aging and many age‐related conditions including arterial and metabolic dysfunction. However, the mechanisms and tissues involved in these beneficial effects remain largely unknown. Here, we demonstrate that activation of S6K, a downstream target of mTOR, is increased in arteries with advancing age, and that this occurs preferentially in the endothelium compared with the vascular smooth muscle. Induced endothelial cell‐specific deletion of mTOR reduced protein expression by 60–70%. Although this did not significantly alter arterial and metabolic function in young mice, endothelial mTOR reduction reversed arterial stiffening and improved endothelium‐dependent dilation (EDD) in old mice, indicating an improvement in age‐related arterial dysfunction. Improvement in arterial function in old mice was concomitant with reductions in arterial cellular senescence, inflammation, and oxidative stress. The reduction in endothelial mTOR also improved glucose tolerance in old mice, and this was associated with attenuated hepatic gluconeogenesis and improved lipid tolerance, but was independent of alterations in peripheral insulin sensitivity, pancreatic beta cell function, or fasted plasma lipids in old mice. Lastly, we found that endothelial mTOR reduction suppressed gene expression of senescence and inflammatory markers in endothelial‐rich (i.e., lung) and metabolically active organs (i.e., liver and adipose tissue), which may have contributed to the improvement in metabolic function in old mice. This is the first evidence demonstrating that reducing endothelial mTOR in old age improves arterial and metabolic function. These findings have implications for future drug development. [ABSTRACT FROM AUTHOR]
Copyright of Aging Cell is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:14749718
DOI:10.1111/acel.14040