Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, USA.
Institute On the Biology of Aging and Metabolism, Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN, 55455, USA.
Geroscience. 2022 Feb;44(1):503-518. doi: 10.1007/s11357-021-00490-3. Epub 2021 Nov 25.
MicroRNAs (miRNAs) are potent regulators of multiple biological processes. Previous studies have demonstrated that miR-146a-5p increases in normal mice during aging, while long-living Ames dwarf (df/df) mice maintain youthful levels of this miRNA. The aim of this study was to elucidate the involvement of miR-146a-5p in modulating cellular senescence and apoptosis in visceral adipose tissue of df/df mice and cultured pre-adipocytes. To test the effects of miR-146a-5p overexpression on visceral adipose tissue, wild-type, and df/df mice, were treated with miRNA-negative control-base and df/df were transfected with 4 or 8 µg/g of a miR-146a-5p mimetic, respectively. Effects of miR-146a-5p overexpression were also evaluated in 3T3-L1 cells cultured under high and normal glucose conditions. Treatment with miR-146a-5p mimetic increased cellular senescence and inflammation and decreased pro-apoptotic factors in visceral adipose tissue of df/df mice. The miR-146a-5p mimetic induced similar effects in 3T3-L1 cells cultivated at normal but not high glucose levels. Importantly, 3T3-L1 HG cells in high glucose conditions showed significantly higher expression of miR-146a-5p than 3T3-L1 grown in normal glucose conditions. These results indicate that miR-146a-5p can be a marker for cellular senescence. This miRNA represents one of the significant SASP factors that if not precisely regulated, can accentuate inflammatory responses and stimulate senescence in surrounding non-senescent cells. The role of miR-146a-5p is different in healthy versus stressed cells, suggesting potential effects of this miRNA depend on overall organismal health, aging, and metabolic state.
微小 RNA(miRNA)是多种生物学过程的有效调节剂。先前的研究表明,miR-146a-5p 在正常衰老的小鼠中增加,而长寿的 Ames 侏儒(df/df)小鼠保持这种 miRNA 的年轻水平。本研究旨在阐明 miR-146a-5p 在调节 df/df 小鼠和培养前体脂肪细胞内脏脂肪组织细胞衰老和细胞凋亡中的作用。为了测试 miR-146a-5p 过表达对内脏脂肪组织的影响,用 miRNA 阴性对照物分别处理野生型和 df/df 小鼠,并用 4 或 8μg/g 的 miR-146a-5p 模拟物转染 df/df。还在高糖和正常葡萄糖条件下培养的 3T3-L1 细胞中评价了 miR-146a-5p 过表达的影响。miR-146a-5p 模拟物的处理增加了 df/df 小鼠内脏脂肪组织中的细胞衰老和炎症,降低了促凋亡因子。miR-146a-5p 模拟物在正常而非高葡萄糖水平培养的 3T3-L1 细胞中诱导了类似的作用。重要的是,在高葡萄糖条件下的 3T3-L1 HG 细胞比在正常葡萄糖条件下生长的 3T3-L1 细胞表现出显著更高水平的 miR-146a-5p。这些结果表明,miR-146a-5p 可以作为细胞衰老的标志物。这种 miRNA 是 SASP 因子的重要代表之一,如果不能精确调节,它可以加重炎症反应并刺激周围非衰老细胞的衰老。miR-146a-5p 在健康细胞和应激细胞中的作用不同,这表明这种 miRNA 的潜在作用取决于整体机体健康、衰老和代谢状态。