: Obesity and type 2 diabetes cause a loss in brown adipose tissue (BAT) activity, but the molecular mechanisms that drive BAT cell remodeling remain largely unexplored. Using a multilayered approach, we comprehensively mapped a reorganization in BAT cells. We uncovered a subset of macrophages as lipid-associated macrophages (LAMs), which were massively increased in genetic and dietary model of BAT expansion. LAMs participate in this scenario by capturing extracellular vesicles carrying damaged lipids and mitochondria released from metabolically stressed brown adipocytes. CD36 scavenger receptor drove LAM phenotype, and CD36-deficient LAMs were able to increase brown fat genes in adipocytes. LAMs released transforming growth factor β1 (TGF-β1), which promoted the loss of brown adipocyte identity through aldehyde dehydrogenase 1 family member A1 (Aldh1a1) induction. These findings unfold cell dynamic changes in BAT during obesity and identify LAMs as key responders to tissue metabolic stress and drivers of loss of brown adipocyte identity.
Lipid-associated macrophages reshape BAT cell identity in obesity / Sciarretta, Francesca; Ninni, Andrea; Zaccaria, Fabio; Chiurchiù, Valerio; Bertola, Adeline; Karlinsey, Keaton; Jia, Wentong; Ceci, Veronica; Di Biagio, Claudia; Xu, Ziyan; Gaudioso, Francesco; Tortolici, Flavia; Tiberi, Marta; Zhang, Jiabi; Carotti, Simone; Boudina, Sihem; Grumati, Paolo; Zhou, Beiyan; Brestoff, Jonathan R; Ivanov, Stoyan; Aquilano, Katia; Lettieri-Barbato, Daniele. - In: CELL REPORTS. - ISSN 2211-1247. - 43:7(2024). [10.1016/j.celrep.2024.114447]
Lipid-associated macrophages reshape BAT cell identity in obesity
Grumati, Paolo;
2024
Abstract
: Obesity and type 2 diabetes cause a loss in brown adipose tissue (BAT) activity, but the molecular mechanisms that drive BAT cell remodeling remain largely unexplored. Using a multilayered approach, we comprehensively mapped a reorganization in BAT cells. We uncovered a subset of macrophages as lipid-associated macrophages (LAMs), which were massively increased in genetic and dietary model of BAT expansion. LAMs participate in this scenario by capturing extracellular vesicles carrying damaged lipids and mitochondria released from metabolically stressed brown adipocytes. CD36 scavenger receptor drove LAM phenotype, and CD36-deficient LAMs were able to increase brown fat genes in adipocytes. LAMs released transforming growth factor β1 (TGF-β1), which promoted the loss of brown adipocyte identity through aldehyde dehydrogenase 1 family member A1 (Aldh1a1) induction. These findings unfold cell dynamic changes in BAT during obesity and identify LAMs as key responders to tissue metabolic stress and drivers of loss of brown adipocyte identity.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
