Rivera-Gonzalez Guillermo C, Shook Brett A, Andrae Johanna, Holtrup Brandon, Bollag Katherine, Betsholtz Christer, Rodeheffer Matthew S, Horsley Valerie
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Cell Stem Cell. 2016 Dec 1;19(6):738-751. doi: 10.1016/j.stem.2016.09.002. Epub 2016 Oct 13.
Tissue growth and maintenance requires stem cell populations that self-renew, proliferate, and differentiate. Maintenance of white adipose tissue (WAT) requires the proliferation and differentiation of adipocyte stem cells (ASCs) to form postmitotic, lipid-filled mature adipocytes. Here we use the dynamic adipogenic program that occurs during hair growth to uncover an unrecognized regulator of ASC self-renewal and proliferation, PDGFA, which activates AKT signaling to drive and maintain the adipogenic program in the skin. Pdgfa expression is reduced in aged ASCs and is required for ASC proliferation and maintenance in the dermis, but not in other WATs. Our molecular and genetic studies uncover PI3K/AKT2 as a direct PDGFA target that is activated in ASCs during WAT hyperplasia and is functionally required for dermal ASC proliferation. Our data therefore reveal active mechanisms that regulate ASC self-renewal in the skin and show that distinct regulatory mechanisms operate in different WAT depots.
组织生长和维持需要具有自我更新、增殖和分化能力的干细胞群。白色脂肪组织(WAT)的维持需要脂肪干细胞(ASC)增殖和分化,以形成不再分裂、充满脂质的成熟脂肪细胞。在这里,我们利用毛发生长过程中发生的动态脂肪生成程序,发现了一种未被识别的ASC自我更新和增殖调节因子——血小板衍生生长因子A(PDGFA),它激活AKT信号传导,以驱动和维持皮肤中的脂肪生成程序。在衰老的ASC中,Pdgfa表达降低,它是真皮中ASC增殖和维持所必需的,但在其他WAT中并非如此。我们的分子和遗传学研究发现PI3K/AKT2是PDGFA的直接靶点,在WAT增生过程中,它在ASC中被激活,并且是真皮ASC增殖所必需的功能靶点。因此,我们的数据揭示了调节皮肤中ASC自我更新的活跃机制,并表明不同的调节机制在不同的WAT储存部位发挥作用。