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肥胖相关的miR-1908在人脂肪细胞中的表达受脂肪因子、游离脂肪酸和激素的调节。

Expression of obesity‑related miR‑1908 in human adipocytes is regulated by adipokines, free fatty acids and hormones.

作者信息

Jiang Xinye, Yang Lei, Pang Lingxia, Chen Ling, Guo Xirong, Ji Chenbo, Shi Chunmei, Ni Yuhui

机构信息

Department of Child Health Care, Wuxi Maternal and Child Health Hospital, Wuxi, Jiangsu 214002, P.R. China.

Institute of Pediatrics, Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.

出版信息

Mol Med Rep. 2014 Aug;10(2):1164-9. doi: 10.3892/mmr.2014.2297. Epub 2014 Jun 5.

Abstract

White adipose tissue mass is governed by competing processes that control lipid synthesis and storage, as well as the development of new adipocytes, and also trigger metabolic and inflammatory changes. microRNAs (miRNAs) have been suggested to act as negative regulators controlling varied biological processes at the level of post‑transcriptional repression. The present study focused on investigating the expression of miR‑1908 in mature human adipocytes and its responses to adipokines [tumor necrosis factor α (TNF‑α), interleukin 6 (IL‑6), leptin and resistin), free fatty acids (FFAs), growth hormone (GH) and dexamethasone (DEX). miR‑1908 was highly expressed in mature human adipocytes. The mature human adipocytes responded to proinflammatory cytokines (TNF‑α and IL‑6) by markedly increasing the expression of miR‑1908 at 4 h of incubation. Adipokines (resistin and leptin) and FFAs were shown to downregulate the expression of miR‑1908 in human adipocytes. Furthermore, the expression of miR‑1908 was decreased 4 h after treatment with GH; however, DEX treatment of human adipocytes did not affect the expression of miR‑1908 during the 24‑h experimental period. In conclusion, the present study showed that the expression of miR‑1908 is affected by a variety of factors that are associated with obesity and insulin sensitivity. miR‑1908 may be an important mediator in the development of obesity‑related complications.

摘要

白色脂肪组织量受控制脂质合成与储存、新脂肪细胞发育以及引发代谢和炎症变化的相互竞争过程所支配。微小RNA(miRNA)被认为是在转录后抑制水平控制多种生物学过程的负调节因子。本研究聚焦于调查miR-1908在成熟人类脂肪细胞中的表达及其对脂肪因子[肿瘤坏死因子α(TNF-α)、白细胞介素6(IL-6)、瘦素和抵抗素]、游离脂肪酸(FFA)、生长激素(GH)和地塞米松(DEX)的反应。miR-1908在成熟人类脂肪细胞中高表达。成熟人类脂肪细胞在孵育4小时时通过显著增加miR-1908的表达来响应促炎细胞因子(TNF-α和IL-6)。脂肪因子(抵抗素和瘦素)和FFA被证明可下调人类脂肪细胞中miR-1908的表达。此外,用GH处理4小时后miR-1908的表达降低;然而,在24小时实验期内,DEX处理人类脂肪细胞并未影响miR-1908的表达。总之,本研究表明miR-1908的表达受多种与肥胖和胰岛素敏感性相关的因素影响。miR-1908可能是肥胖相关并发症发生发展中的一个重要介质。

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