Institute for Diabetes, Obesity and Metabolism, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Cell and Developmental Biology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Science. 2019 Apr 26;364(6438). doi: 10.1126/science.aav2501.
Metabolic health depends on the capacity of adipose tissue progenitor cells to undergo de novo adipogenesis. The cellular hierarchy and mechanisms governing adipocyte progenitor differentiation are incompletely understood. Through single-cell RNA sequence analyses, we show that the lineage hierarchy of adipocyte progenitors consists of distinct mesenchymal cell types that are present in both mouse and human adipose tissues. Cells marked by dipeptidyl peptidase-4 (DPP4)/CD26 expression are highly proliferative, multipotent progenitors. During the development of subcutaneous adipose tissue in mice, these progenitor cells give rise to intercellular adhesion molecule-1 (ICAM1)/CD54-expressing (CD54+) committed preadipocytes and a related adipogenic cell population marked by and /CD142 expression. Transforming growth factor-β maintains DPP4+ cell identity and inhibits adipogenic commitment of DPP4+ and CD142+ cells. Notably, DPP4+ progenitors reside in the reticular interstitium, a recently appreciated fluid-filled space within and between tissues, including adipose depots.
代谢健康取决于脂肪组织祖细胞进行从头脂肪生成的能力。脂肪细胞祖细胞分化的细胞层次结构和机制尚不完全清楚。通过单细胞 RNA 序列分析,我们表明脂肪细胞祖细胞的谱系层次结构由不同的间充质细胞类型组成,这些细胞类型存在于小鼠和人类脂肪组织中。表达二肽基肽酶-4(DPP4)/CD26 的细胞是高度增殖的多能祖细胞。在小鼠皮下脂肪组织的发育过程中,这些祖细胞产生细胞间黏附分子-1(ICAM1)/CD54 表达(CD54+)的定向前脂肪细胞和一个由 和 /CD142 表达标记的相关脂肪生成细胞群体。转化生长因子-β维持 DPP4+细胞的特性,并抑制 DPP4+和 CD142+细胞的脂肪生成定向。值得注意的是,DPP4+祖细胞位于网状间质中,这是一个最近才被认识到的充满液体的空间,存在于组织内和组织之间,包括脂肪组织。