Li Liang, Feldman Brian J
Department of Pediatrics, University of California, San Francisco (UCSF) School of Medicine, San Francisco, CA 94158, USA; Department of Pediatrics, Yale School of Medicine, New Haven, CT 06520, USA.
Stem Cell Reports. 2025 Jun 10;20(6):102509. doi: 10.1016/j.stemcr.2025.102509. Epub 2025 May 22.
Enhancing energy utilization by increasing the number or activity of beige adipocytes has the potential to be of therapeutic benefit for a broad range of metabolic disorders. However, knowledge gaps in our understanding of the mouse versus human developmental origins of beige fat have inhibited the generation of robust preclinical models, leaving a barrier to the success of therapies. Here, we report that a distinct inguinal beige adipose tissue (ibAT) depot lineage traces to the same Prx1+ cell origins as inguinal white adipose tissue (iWAT) but maintains higher thermogenic activity and capability during aging. We discovered that ibAT has the morphological appearance of human supraclavicular brown adipose tissue (scBAT) and, importantly, conserved molecular markers and developmental origins with human scBAT. Our findings reveal a distinct mouse beige adipose tissue depot and provide a preclinical model of human beige adipose tissue development and maintenance.
通过增加米色脂肪细胞的数量或活性来提高能量利用,对于广泛的代谢紊乱具有潜在的治疗益处。然而,我们对小鼠与人类米色脂肪发育起源的理解存在知识空白,这阻碍了强大的临床前模型的建立,成为治疗成功的障碍。在这里,我们报告一个独特的腹股沟米色脂肪组织(ibAT)库的谱系与腹股沟白色脂肪组织(iWAT)起源于相同的Prx1+细胞,但在衰老过程中保持较高的产热活性和能力。我们发现ibAT具有人类锁骨上棕色脂肪组织(scBAT)的形态外观,重要的是,与人类scBAT具有保守的分子标记和发育起源。我们的研究结果揭示了一种独特的小鼠米色脂肪组织库,并提供了人类米色脂肪组织发育和维持的临床前模型。