Key result
PPAR-γ activation differentiates human adipose stromal cells into beige adipocytes capable of UCP1-dependent thermogenesis.
Why the study?
Human white adipose tissue-derived beige adipocytes have potential for treating obesity and type 2 diabetes, but their thermogenic capacity and mechanisms require clarification.
Human white fat-derived progenitor cells can be converted into beige adipocytes capable of UCP1-dependent thermogenesis, offering a potential therapeutic target for obesity and type 2 diabetes.
Beige adipocyte conversion from hASCs is feasible in vitro; leaves open therapeutic translation for obesity or diabetes.
Heat-producing beige/brite (brown-in-white) adipocytes in white adipose tissue have the potential to suppress metabolic disease in mice and hold great promise for the treatment of obesity and type 2 diabetes in humans. Here, we demonstrate that human adipose-derived stromal/progenitor cells (hASCs) from subcutaneous white adipose tissue can be efficiently converted into beige adipocytes. Upon pharmacological activation of peroxisome proliferator-activated receptor-γ, hASC-derived adipocytes activated beige fat-selective genes and a brown/beige fat-selective electron transport chain gene program. Importantly, hASC-derived beige fat cells displayed the bioenergetic characteristics of genuine brown fat cells, including a capacity for increased respiratory uncoupling in response to β-adrenergic agonists. Furthermore, knock-down experiments reveal that the thermogenic capacity of human beige fat cells was entirely dependent on the presence of Uncoupling protein 1. In summary, this study reveals that hASCs can be readily differentiated into beige adipocytes that, upon activation, undergo uncoupling protein 1-dependent thermogenesis.
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Bartesaghi et al. (2014) studied this question. Pharmacological activation of PPAR-γ and UCP1 knock-down was evaluated on Thermogenic capacity and bioenergetic characteristics. Human adipose-derived stromal cells can be differentiated into beige adipocytes that undergo UCP1-dependent thermogenesis upon activation.
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