Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Institute for Diabetes, Obesity and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Research and Development BioRestorative Therapies, New York, NY 11747, USA.
Cell Rep. 2020 Mar 3;30(9):3079-3091.e5. doi: 10.1016/j.celrep.2020.02.032.
Brown adipose tissue (BAT) generates heat to maintain body temperature and suppress obesity. Agonists for nuclear receptors PPARα and PPARγ both affect brown adipocyte function, yet the interplay between these factors in BAT is uncertain. Here, we report that PPARα shares most genomic binding sites with PPARγ, and these common binding sites are more related to BAT function than PPARγ-selective sites without PPARα. Integrating PPARα and PPARγ genomic occupancy with cold-responsive BAT transcriptomes identifies a subset of 16 genes with potential relevance to BAT function. Among these, we focused on the lysosomal protease cathepsin Z (CTSZ) and showed it is necessary for mitochondrial respiration in both mouse and human brown adipocytes. Thus, CTSZ is a shared PPARα/γ target gene in BAT and a regulator of brown adipocyte thermogenic function.
棕色脂肪组织 (BAT) 产生热量以维持体温并抑制肥胖。核受体 PPARα 和 PPARγ 的激动剂都影响棕色脂肪细胞的功能,但这些因素在 BAT 中的相互作用尚不确定。在这里,我们报告 PPARα 与 PPARγ 共享大多数基因组结合位点,并且这些共同结合位点与 BAT 功能的关系比没有 PPARα 的 PPARγ 选择性结合位点更为密切。将 PPARα 和 PPARγ 的基因组占据与冷响应的 BAT 转录组相结合,确定了一组 16 个与 BAT 功能相关的潜在基因。在这些基因中,我们重点关注溶酶体蛋白酶组织蛋白酶 Z (CTSZ),并表明其对于人和小鼠的棕色脂肪细胞的线粒体呼吸是必需的。因此,CTSZ 是 BAT 中 PPARα/γ 的共同靶基因,也是棕色脂肪细胞产热功能的调节剂。