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驻留巨噬细胞抑制肥胖小鼠病理性脂肪组织重构,保护血管完整性。

Resident macrophages restrain pathological adipose tissue remodeling and protect vascular integrity in obese mice.

机构信息

School of Biological Sciences, Nanyang Technological University, Singapore City, Singapore.

SIgN, A*Star, Singapore City, Singapore.

出版信息

EMBO Rep. 2021 Aug 4;22(8):e52835. doi: 10.15252/embr.202152835. Epub 2021 Jul 1.

Abstract

Tissue-resident macrophages in white adipose tissue (WAT) dynamically adapt to the metabolic changes of their microenvironment that are often induced by excess energy intake. Currently, the exact contribution of these macrophages in obesity-driven WAT remodeling remains controversial. Here, using a transgenic CD169-DTR mouse strain, we provide new insights into the interplay between CD169 adipose tissue macrophages (ATMs) and their surrounding WAT microenvironment. Using targeted in vivo ATM ablation followed by transcriptional and metabolic WAT profiling, we found that ATMs protect WAT from the excessive pathological remodeling that occurs during obesity. As obesity progresses, ATMs control not only vascular integrity, adipocyte function, and lipid and metabolic derangements but also extracellular matrix accumulation and resultant fibrosis in the WAT. The protective role of ATMs during obesity-driven WAT dysfunction supports the notion that ATMs represent friends, rather than foes, as has previously assumed.

摘要

白色脂肪组织(WAT)中的组织驻留巨噬细胞可以动态适应其微环境的代谢变化,而这些变化通常是由能量摄入过多引起的。目前,这些巨噬细胞在肥胖驱动的 WAT 重塑中的确切贡献仍存在争议。在这里,我们使用一种转基因 CD169-DTR 小鼠品系,深入了解了 CD169 脂肪组织巨噬细胞(ATMs)与其周围 WAT 微环境之间的相互作用。通过靶向体内 ATM 消融,以及随后的转录组和代谢组 WAT 分析,我们发现 ATMs 可保护 WAT 免受肥胖期间发生的过度病理性重塑。随着肥胖的进展,ATMs 不仅控制血管完整性、脂肪细胞功能和脂质及代谢紊乱,还控制细胞外基质的积累和 WAT 中的纤维化。在肥胖驱动的 WAT 功能障碍期间,ATMs 发挥保护作用,这一事实支持了之前的观点,即 ATMs 是朋友而不是敌人。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e4b/8339675/b610eca49899/EMBR-22-e52835-g010.jpg

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