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CITED2 介导机械负荷诱导的髌下脂肪垫脂肪因子的抑制作用。

CITED2 mediates the mechanical loading-induced suppression of adipokines in the infrapatellar fat pad.

机构信息

Department of Orthopaedic Surgery, Albert Einstein College of Medicine, Bronx, New York.

Department of Spine Surgery, Jilin Provincial Key Laboratory of Tissue Repair, Reconstruction and Regeneration, The First Hospital of Jilin University, Jilin, China.

出版信息

Ann N Y Acad Sci. 2019 Apr;1442(1):153-164. doi: 10.1111/nyas.14025. Epub 2019 Mar 19.

Abstract

Adipokines secreted from the infrapatellar fat pad (IPFP), such as adipsin and adiponectin, have been implicated in osteoarthritis pathogenesis. CITED2, a mechanosensitive transcriptional regulator with chondroprotective activity, may modulate their expression. Cited2 haploinsufficient mice (Cited2 ) on a high-fat diet (HFD) exhibited increased body weight and increased IPFP area compared to wild-type (WT) mice on an HFD. While an exercise regimen of moderate treadmill running induced the expression of CITED2, as well as PGC-1α, and reduced the expression of adipsin and adiponectin in the IPFP of WT mice on an HFD, Cited2 haploinsufficiency abolished the loading-induced expression of PGC-1α and loading-induced suppression of adipsin and adiponectin. Furthermore, knocking down or knocking out CITED2 in adipose stem cells (ASCs)/preadipocytes derived from the IPFP in vitro led to the increased expression of adipsin and adiponectin and reduced PGC-1α, and abolished the loading-induced suppression of adipsin and adiponectin and loading-induced expression of PGC-1α. Overexpression of PGC-1α in these ASC/preadipocytes reversed the effects caused by CITED2 deficiency. The current data suggest that CITED2 is a critical regulator in physiologic loading-induced chondroprotection in the context of an HFD and PGC-1α is required for the inhibitory effects of CITED2 on the expression of adipokines such as adipsin and adiponectin in the IPFP.

摘要

从髌下脂肪垫(IPFP)分泌的脂肪因子,如脂联素和脂联素,与骨关节炎的发病机制有关。具有软骨保护活性的机械敏感转录调节因子 CITED2 可能调节它们的表达。高脂饮食(HFD)条件下 Cited2 杂合不足(Cited2 )的小鼠与 HFD 条件下的野生型(WT)小鼠相比,体重增加,IPFP 面积增加。虽然适度的跑步机跑步运动方案诱导了 CITED2 的表达,以及 PGC-1α 的表达,并降低了 HFD 条件下 WT 小鼠 IPFP 中脂联素和脂联素的表达,但 Cited2 杂合不足消除了负载诱导的 PGC-1α 的表达和负载诱导的脂联素和脂联素的抑制。此外,体外敲低或敲除源自 IPFP 的脂肪干细胞(ASCs)/前脂肪细胞中的 CITED2 导致脂联素和脂联素的表达增加,PGC-1α 减少,并消除了负载诱导的脂联素和脂联素的抑制和负载诱导的 PGC-1α 的表达。这些 ASC/前脂肪细胞中 PGC-1α 的过表达逆转了 CITED2 缺乏引起的效应。目前的数据表明,CITED2 是 HFD 条件下生理负荷诱导的软骨保护中的关键调节因子,PGC-1α 是 CITED2 对 IPFP 中脂联素和脂联素等脂肪因子表达的抑制作用所必需的。

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