Matsushita Yuki, Chu Angel Ka Yan, Ono Wanida, Welch Joshua D, Ono Noriaki
University of Michigan School of Dentistry, Ann Arbor, MI, USA.
Department of Computational Medicine and Bioinformatics, Department of Computer Science and Engineering, University of Michigan, Ann Arbor, MI, USA.
J Bone Miner Res. 2021 Jun;36(6):1145-1158. doi: 10.1002/jbmr.4282. Epub 2021 Mar 16.
Bone marrow houses a multifunctional stromal cell population expressing C-X-C motif chemokine ligand 12 (CXCL12), termed CXCL12-abundant reticular (CAR) cells, that regulates osteogenesis and adipogenesis. The quiescent pre-adipocyte-like subset of CXCL12 stromal cells ("Adipo-CAR" cells) is localized to sinusoidal surfaces and particularly enriched for hematopoiesis-supporting cytokines. However, detailed characteristics of these CXCL12 pre-adipocyte-like stromal cells and how they contribute to marrow adipogenesis remain largely unknown. Here we highlight CXCL12-dependent physical coupling with hematopoietic cells as a potential mechanism regulating the adipogenic potential of CXCL12 stromal cells. Single-cell computational analyses of RNA velocity and cell signaling reveal that Adipo-CAR cells exuberantly communicate with hematopoietic cells through CXCL12-CXCR4 ligand-receptor interactions but do not interconvert with Osteo-CAR cells. Consistent with this computational prediction, a substantial fraction of Cxcl12-creER pre-adipocyte-like cells intertwines with hematopoietic cells in vivo and in single-cell preparation in a protease-sensitive manner. Deletion of CXCL12 in these cells using Col2a1-cre leads to a reduction of stromal-hematopoietic coupling and extensive marrow adipogenesis in adult bone marrow, which appears to involve direct conversion of CXCL12 cells to lipid-laden marrow adipocytes without altering mesenchymal progenitor cell fates. Therefore, these findings suggest that CXCL12 pre-adipocyte-like marrow stromal cells prevent their premature differentiation by maintaining physical coupling with hematopoietic cells in a CXCL12-dependent manner, highlighting a possible cell-non-autonomous mechanism that regulates marrow adipogenesis. © 2021 American Society for Bone and Mineral Research (ASBMR).
骨髓中存在一种多功能基质细胞群体,其表达C-X-C基序趋化因子配体12(CXCL12),称为富含CXCL12的网状(CAR)细胞,该细胞群体可调节成骨作用和脂肪生成。CXCL12基质细胞的静止前脂肪细胞样亚群(“脂肪CAR”细胞)定位于窦状表面,尤其富含支持造血的细胞因子。然而,这些CXCL12前脂肪细胞样基质细胞的详细特征以及它们如何促进骨髓脂肪生成在很大程度上仍不清楚。在这里,我们强调CXCL12依赖的与造血细胞的物理偶联是调节CXCL12基质细胞脂肪生成潜能的一种潜在机制。对RNA速度和细胞信号的单细胞计算分析表明,脂肪CAR细胞通过CXCL12-CXCR4配体-受体相互作用与造血细胞进行旺盛的通讯,但不会与骨CAR细胞相互转化。与这一计算预测一致,在体内和单细胞制备中,相当一部分Cxcl12-creER前脂肪细胞样细胞以蛋白酶敏感的方式与造血细胞缠绕在一起。使用Col2a1-cre在这些细胞中删除CXCL12会导致成年骨髓中基质-造血偶联减少和广泛的骨髓脂肪生成,这似乎涉及CXCL12细胞直接转化为充满脂质的骨髓脂肪细胞,而不改变间充质祖细胞的命运。因此,这些发现表明,CXCL12前脂肪细胞样骨髓基质细胞通过以CXCL12依赖的方式与造血细胞保持物理偶联来防止其过早分化,突出了一种可能调节骨髓脂肪生成的细胞非自主机制。©2021美国骨与矿物质研究学会(ASBMR)。