| Literature DB >> 31503545 |
Zhuzhen Zhang1, Mengle Shao1, Chelsea Hepler1, Zhenzhen Zi2, Shangang Zhao1, Yu A An1, Yi Zhu1, Alexandra L Ghaben1, May-Yun Wang1, Na Li1, Toshiharu Onodera1, Nolwenn Joffin1, Clair Crewe1, Qingzhang Zhu1, Lavanya Vishvanath1, Ashwani Kumar3, Chao Xing3, Qiong A Wang4, Laurent Gautron5, Yingfeng Deng1, Ruth Gordillo1, Ilja Kruglikov6, Christine M Kusminski1, Rana K Gupta1, Philipp E Scherer1.
Abstract
Dermal adipose tissue (also known as dermal white adipose tissue and herein referred to as dWAT) has been the focus of much discussion in recent years. However, dWAT remains poorly characterized. The fate of the mature dermal adipocytes and the origin of the rapidly reappearing dermal adipocytes at different stages remain unclear. Here, we isolated dermal adipocytes and characterized dermal fat at the cellular and molecular level. Together with dWAT's dynamic responses to external stimuli, we established that dermal adipocytes are a distinct class of white adipocytes with high plasticity. By combining pulse-chase lineage tracing and single-cell RNA sequencing, we observed that mature dermal adipocytes undergo dedifferentiation and redifferentiation under physiological and pathophysiological conditions. Upon various challenges, the dedifferentiated cells proliferate and redifferentiate into adipocytes. In addition, manipulation of dWAT highlighted an important role for mature dermal adipocytes for hair cycling and wound healing. Altogether, these observations unravel a surprising plasticity of dermal adipocytes and provide an explanation for the dynamic changes in dWAT mass that occur under physiological and pathophysiological conditions, and highlight the important contributions of dWAT toward maintaining skin homeostasis.Entities:
Keywords: Adipose tissue; Dermatology; Metabolism; Mouse models
Mesh:
Year: 2019 PMID: 31503545 PMCID: PMC6877341 DOI: 10.1172/JCI130239
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808