Center for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, ME 04074, USA.
Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA; UPMC Hillman Cancer Center, Pittsburgh, PA 15213, USA.
Cell Rep. 2018 Dec 11;25(11):3215-3228.e9. doi: 10.1016/j.celrep.2018.11.037.
Molecular- and cellular-based therapies have the potential to reduce obesity-associated disease. In response to cold, beige adipocytes form in subcutaneous white adipose tissue and convert energy stored in metabolic substrates to heat, making them an attractive therapeutic target. We developed a robust method to generate a renewable source of human beige adipocytes from induced pluripotent stem cells (iPSCs). Developmentally, these cells are derived from FOXF1 mesoderm and progress through an expandable mural-like mesenchymal stem cell (MSC) to form mature beige adipocytes that display a thermogenically active profile. This includes expression of uncoupling protein 1 (UCP1) concomitant with increased uncoupled respiration. With this method, dysfunctional adipogenic precursors can be reprogrammed and differentiated into beige adipocytes with increased thermogenic function and anti-diabetic secretion potential. This resource can be used to (1) elucidate mechanisms that underlie the control of beige adipogenesis and (2) generate material for cellular-based therapies that target metabolic syndrome in humans.
基于分子和细胞的疗法有可能减少与肥胖相关的疾病。为了应对寒冷,米色脂肪细胞在皮下白色脂肪组织中形成,并将代谢底物中储存的能量转化为热量,这使它们成为一个有吸引力的治疗靶点。我们开发了一种从诱导多能干细胞(iPSC)生成可再生人类米色脂肪细胞的方法。从发育上看,这些细胞来源于 FOXF1 中胚层,并通过可扩展的壁状间充质干细胞(MSC)发育,形成成熟的米色脂肪细胞,表现出产热活性特征。这包括解偶联蛋白 1(UCP1)的表达伴随着解偶联呼吸的增加。通过这种方法,可以重新编程功能失调的脂肪生成前体,并将其分化为米色脂肪细胞,增加产热功能和抗糖尿病分泌潜能。这种资源可用于:(1)阐明控制米色脂肪生成的机制;(2)为针对人类代谢综合征的细胞疗法生成材料。