脂肪组织
干细胞
炎症
细胞生物学
胰岛素抵抗
干细胞疗法
免疫系统
线粒体
生物
胰岛素
内分泌学
平衡
葡萄糖稳态
妊娠期糖尿病
脂解
糖尿病
重编程
内科学
白色脂肪组织
营养感应
化学
线粒体生物发生
细胞疗法
微泡
细胞
医学
机制(生物学)
细胞器生物发生
癌症研究
脂肪因子
作者
Bingnan Chen,Xuyang Chen,Jian‐Xin Li,Ruohan Hu,Lijun Yang,Hongli Li,Xiaoan Liu,Richard D. Cannon,Richard Saffery,Boris Novakovic,Hongbo Qi,Hua Zhang,Xiaobo Zhou
出处
期刊:Cell Reports
[Cell Press]
日期:2025-11-01
卷期号:44 (11): 116505-116505
被引量:1
标识
DOI:10.1016/j.celrep.2025.116505
摘要
Adipose-derived stem cells (ADSCs) represent a promising therapeutic resource, yet their immunometabolic regulation remains poorly defined. Here, we reveal a tunneling nanotube (TNT)-mediated communication mechanism between ADSCs and adipose tissue macrophages (ATMs) that maintains metabolic homeostasis during pregnancy. Using gestational diabetes mellitus (GDM) mouse models combined with live-cell imaging, scanning electron microscope, and multi-omics approaches, we demonstrate that mitochondrial transfer from ADSCs to ATMs via TNTs sustains ATM metabolic fitness. This process is governed by the WNT5A-RhoA-ROCK1 axis and becomes impaired under metabolic stress, driving ATMs inflammatory polarization and insulin resistance. Importantly, in situ ADSC administration restores mitochondrial transfer and improves metabolic parameters in GDM mice. Collectively, our work establishes TNT-mediated organelle sharing as a fundamental mechanism of stem cell-immune interaction and demonstrates that ADSC-based therapy represents a promising strategy for GDM by reprogramming the metabolism of immune cells.
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