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饱和脂肪酸通过 PERK/eIF2/CHOP 信号通路促进人巨噬细胞中 GDF15 的表达。

Saturated Fatty Acids Promote GDF15 Expression in Human Macrophages through the PERK/eIF2/CHOP Signaling Pathway.

机构信息

Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID, University of Lille, F-59000 Lille, France.

Laboratory of Virology and Immunology, University of Liege, GIGA-Signal Transduction, 4000 Liege, Belgium.

出版信息

Nutrients. 2020 Dec 8;12(12):3771. doi: 10.3390/nu12123771.

Abstract

Growth differentiation factor-15 (GDF-15) and its receptor GFRAL are both involved in the development of obesity and insulin resistance. Plasmatic GDF-15 level increases with obesity and is positively associated with disease progression. Despite macrophages have been recently suggested as a key source of GDF-15 in obesity, little is known about the regulation of GDF-15 in these cells. In the present work, we sought for potential pathophysiological activators of expression in human macrophages and identified saturated fatty acids (SFAs) as strong inducers of expression and secretion. SFAs increase expression through the induction of an ER stress and the activation of the PERK/eIF2/CHOP signaling pathway in both PMA-differentiated THP-1 cells and in primary monocyte-derived macrophages. The transcription factor CHOP directly binds to the promoter region and regulates expression. Unlike SFAs, unsaturated fatty acids do not promote expression and rather inhibit both SFA-induced expression and ER stress. These results suggest that free fatty acids may be involved in the control of GDF-15 and provide new molecular insights about how diet and lipid metabolism may regulate the development of obesity and T2D.

摘要

生长分化因子 15(GDF-15)及其受体 GFRAL 均参与肥胖和胰岛素抵抗的发生。血浆 GDF-15 水平随肥胖而增加,并与疾病进展呈正相关。尽管最近有研究表明巨噬细胞是肥胖症中 GDF-15 的主要来源,但对于这些细胞中 GDF-15 的调控知之甚少。在本研究中,我们在人巨噬细胞中寻找 GDF-15 表达的潜在病理生理激活剂,并确定饱和脂肪酸(SFAs)是 GDF-15 表达和分泌的强诱导剂。SFAs 通过诱导内质网应激和 PERK/eIF2/CHOP 信号通路的激活,增加 PMA 分化的 THP-1 细胞和原代单核细胞衍生的巨噬细胞中的 表达。转录因子 CHOP 直接与 启动子区域结合并调节 表达。与 SFAs 不同,不饱和脂肪酸不会促进 表达,而是抑制 SFA 诱导的 表达和内质网应激。这些结果表明,游离脂肪酸可能参与 GDF-15 的调控,并为饮食和脂质代谢如何调节肥胖和 T2D 的发生提供了新的分子见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f164/7764024/56e529625f17/nutrients-12-03771-g001.jpg

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