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

• Main Authors: Chen, Qi, Lai, Si Min, Xu, Shaohai, Tan, Yingrou, Leong, Keith, Liu, Dehua, Tan, Jia Chi, Naik, Roshan Ratnakar, Barron, Anna M., Adav, Sunil S., Chen, Jinmiao, Chong, Shu Zhen, Ng, Lai Guan, Ruedl, Christiane
• Other Authors: School of Biological Sciences
• Format: Article
• Language: English
• Published: 2022
• Subjects: Science::Biological sciences; Adipocyte Hypertrophy; Fibrosis
• Online Access: https://hdl.handle.net/10356/155110
• Institution: Nanyang Technological University

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.