| Literature DB >> 33606988 |
Stefania Carobbio1, Anne-Claire Guenantin2, Myriam Bahri3, Sonia Rodriguez-Fdez3, Floris Honig3, Ioannis Kamzolas4, Isabella Samuelson2, Kathleen Long3, Sherine Awad5, Dunja Lukovic6, Slaven Erceg7, Andrew Bassett3, Sasha Mendjan8, Ludovic Vallier9, Barry S Rosen3, Davide Chiarugi5, Antonio Vidal-Puig10.
Abstract
Increasing brown adipose tissue (BAT) mass and activation is a therapeutic strategy to treat obesity and complications. Obese and diabetic patients possess low amounts of BAT, so an efficient way to expand their mass is necessary. There is limited knowledge about how human BAT develops, differentiates, and is optimally activated. Accessing human BAT is challenging, given its low volume and anatomical dispersion. These constraints make detailed BAT-related developmental and functional mechanistic studies in humans virtually impossible. We have developed and characterized functionally and molecularly a new chemically defined protocol for the differentiation of human pluripotent stem cells (hPSCs) into brown adipocytes (BAs) that overcomes current limitations. This protocol recapitulates step by step the physiological developmental path of human BAT. The BAs obtained express BA and thermogenic markers, are insulin sensitive, and responsive to β-adrenergic stimuli. This new protocol is scalable, enabling the study of human BAs at early stages of development.Entities:
Keywords: BAT progenitors; brown adipose tissue; development; differentiation; human pluripotent stem cells; thermogenesis
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Year: 2021 PMID: 33606988 PMCID: PMC7940445 DOI: 10.1016/j.stemcr.2021.01.013
Source DB: PubMed Journal: Stem Cell Reports ISSN: 2213-6711 Impact factor: 7.765