Adipose progenitor cell-derived extracellular vesicles suppress macrophage M1 program to alleviate midlife obesity.

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Tác giả: Cai Chen, Xuemei Fan, Jia Gao, Zhichao Gao, Teng Huang, Wen Kong, Shiwei Liu, Yanjun Liu, Chenwei Wang, Cong-Yi Wang, Yi Wang, Guorao Wu, Ke Xiang, Hao Xie, Fei Xiong, Yan Yang, Tuying Yong, Qilin Yu, Tiantian Yue, Shu Zhang, Tongtong Zhang, Wanguang Zhang, Qing Zhou

Ngôn ngữ: eng

Ký hiệu phân loại: 201.4 General classes of religion

Thông tin xuất bản: England : Nature communications , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 727792

Among different age groups, middle-aged individuals are particularly susceptible to obesity, with a 22% higher risk of all-cause mortality. However, the underlying mechanisms remain unclear. In this study, we identify adipose progenitor cells (APCs) in the white adipose tissue (WAT) of middle-aged subjects as potential causes of midlife obesity. Specifically, the extracellular vesicles (EVs) derived from APCs display an impaired ability to mitigate the inflammaging of adipose tissue macrophages (ATMs) in middle-aged individuals. Mechanistically, these EVs, lacking miR-145-5p, fail to suppress the expression of L-selectin in ATMs, thereby facilitating their M1 program via the NF-κB signaling pathway. In contrast, EVs from young APCs effectively inhibit M1 macrophage polarization. Accordingly, targeted liposomes are designed to deliver miR-145-5p mimics to ATMs, which effectively prevent the obesity in middle-aged mice. Collectively, our findings highlight the role of APC-derived EVs in midlife obesity and propose miR-145-5pas a promising therapeutic target for clinical applications.
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