生物
祖细胞
内卷(密宗)
Wnt信号通路
细胞生物学
祖细胞
脂肪生成
褐色脂肪组织
细胞分化
干细胞
基因
内分泌学
脂肪组织
内科学
遗传学
信号转导
间充质干细胞
神经科学
医学
意识
作者
Zan Huang,Zengdi Zhang,Zahra Moazzami,Ryan Heck,Ping Hu,Hezkiel Nanda,Kai Ren,Zhihui Sun,Alessandro Bartolomucci,Yan Gao,Dongjun Chung,Weiyun Zhu,Steven S. Shen,Hai Bin Ruan
出处
期刊:Cell Reports
[Elsevier]
日期:2022-04-01
卷期号:39 (2): 110575-110575
被引量:15
标识
DOI:10.1016/j.celrep.2022.110575
摘要
Human brown adipose tissue (BAT) undergoes progressive involution. This involution process is not recapitulated in rodents, and the underlying mechanisms are poorly understood. Here we show that the interscapular BAT (iBAT) of rabbits whitens rapidly during early adulthood. The transcriptomic remodeling and identity switch of mature adipocytes are accompanied by loss of brown adipogenic competence of progenitors. Single-cell RNA sequencing reveals that rabbit and human iBAT progenitors highly express the FSTL1 gene. When iBAT involutes in rabbits, adipocyte progenitors reduce FSTL1 expression and are refractory to brown adipogenic recruitment. Conversely, FSTL1 is constitutively expressed in mouse iBAT to sustain WNT signaling and prevent involution. Progenitor incompetence and iBAT paucity can be induced in mice by genetic deletion of the Fstl1 gene or ablation of Fstl1+ progenitors. Our results highlight the hierarchy and dynamics of the BAT progenitor compartment and implicate the functional incompetence of FSTL1-expressing progenitors in BAT involution.
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