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不同肥胖及衰老状态下脂肪组织中 p27 和 Cdk2 表达的调控。

Regulation of p27 and Cdk2 Expression in Different Adipose Tissue Depots in Aging and Obesity.

机构信息

Center for Nutrition Research and Department of Nutrition, Food Science and Physiology, University of Navarra, 31008 Pamplona, Spain.

Navarra Institute for Health Research (IdiSNA), 31008 Pamplona, Spain.

出版信息

Int J Mol Sci. 2021 Oct 29;22(21):11745. doi: 10.3390/ijms222111745.

Abstract

Aging usually comes associated with increased visceral fat accumulation, reaching even an obesity state, and favoring its associated comorbidities. One of the processes involved in aging is cellular senescence, which is highly dependent on the activity of the regulators of the cell cycle. The aim of this study was to analyze the changes in the expression of and in different adipose tissue depots during aging, as well as their regulation by obesity in mice. Changes in the expression of and in visceral and subcutaneous white adipose tissue (WAT) biopsies were also analyzed in a human cohort of obesity and type 2 diabetes. , but not , exhibits a lower expression in subcutaneous than in visceral WAT in mice and humans. is drastically downregulated by aging in subcutaneous WAT (scWAT), but not in gonadal WAT, of female mice. Obesity upregulates and expression in scWAT, but not in other fat depots of aged mice. In humans, a significant upregulation of was observed in visceral WAT of subjects with obesity. Taken together, these results show a differential adipose depot-dependent regulation of and in aging and obesity, suggesting that p27 and cdk2 could contribute to the adipose-tissue depot's metabolic differences. Further studies are necessary to fully corroborate this hypothesis.

摘要

衰老通常伴随着内脏脂肪堆积增加,甚至达到肥胖状态,并有利于其相关的合并症。衰老过程中涉及的一个过程是细胞衰老,这高度依赖于细胞周期调节剂的活性。本研究旨在分析在衰老过程中不同脂肪组织中 和 的表达变化,以及肥胖对小鼠中这些基因的调控。还分析了肥胖和 2 型糖尿病人类队列中内脏和皮下白色脂肪组织 (WAT) 活检中 和 的表达变化。与 不同, 在小鼠和人类的皮下 WAT 中的表达低于内脏 WAT。肥胖会使雌性小鼠的皮下 WAT(scWAT)中 的表达急剧下调,但在性腺 WAT 中则不会。肥胖会上调 scWAT 中 和 的表达,但不会上调老年小鼠的其他脂肪组织中的表达。在人类中,肥胖患者的内脏 WAT 中观察到 的表达显著上调。总之,这些结果表明,p27 和 cdk2 在衰老和肥胖过程中对脂肪组织的不同部位具有不同的调节作用,提示 p27 和 cdk2 可能有助于脂肪组织代谢的差异。需要进一步的研究来充分证实这一假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2dc/8584112/6a3d0478fc35/ijms-22-11745-g001.jpg

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