骨膜
骨髓
祖细胞
干细胞
骨愈合
间质细胞
生物
骨细胞
细胞生物学
解剖
免疫学
癌症研究
作者
Elise Jeffery,Terry L.A. Mann,Jade A. Pool,Zhiyu Zhao,Sean J. Morrison
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2022-10-21
卷期号:29 (11): 1547-1561.e6
被引量:136
标识
DOI:10.1016/j.stem.2022.10.002
摘要
A fundamental question in bone biology concerns the contributions of skeletal stem/progenitor cells (SSCs) in the bone marrow versus the periosteum to bone repair. We found that SSCs in adult bone marrow can be identified based on Leprcre and Adiponectin-cre/creER expression while SSCs in adult periosteum can be identified based on Gli1creERT2 expression. Under steady-state conditions, new bone arose primarily from bone marrow SSCs. After bone injuries, both SSC populations began proliferating but made very different contributions to bone repair. Drill injuries were primarily repaired by LepR+/Adiponectin+ bone marrow SSCs. Conversely, bicortical fractures were primarily repaired by Gli1+ periosteal SSCs, though LepR+/Adiponectin+ bone marrow cells transiently formed trabecular bone at the fracture site. Gli1+ periosteal cells also regenerated LepR+ bone marrow stromal cells that expressed hematopoietic niche factors at fracture sites. Different bone injuries are thus repaired by different SSCs, with periosteal cells regenerating bone and marrow stroma after non-stabilized fractures.
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