The Prrx1eGFP Mouse Labels the Periosteum During Development and a Subpopulation of Osteogenic Periosteal Cells in the Adult.
The Prrx1eGFP Mouse Labels the Periosteum During Development and a Subpopulation of Osteogenic Periosteal Cells in the Adult.
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PRRX1EGFP小鼠在成年人中发育过程中标记骨膜的骨膜和成骨细胞的亚群。
DOI:
10.1002/jbm4.10707
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发表时间:
2023-03
期刊:
影响因子:
3.8
通讯作者:
Logan, Malcolm P. O.
中科院分区:
文献类型:
--
作者:
Brown, Sarah;Malik, Saif;Aljammal, Maria;O'Flynn, Aine;Hobbs, Carl;Shah, Mittal;Roberts, Scott J.;Logan, Malcolm P. O.
The identity of the cells that form the periosteum during development is controversial with current dogma suggesting these are derived from a Sox9‐positive progenitor. Herein, we characterize a newly created Prrx1eGFP reporter transgenic mouse line during limb formation and postnatally. Interestingly, in the embryo Prrx1eGFP‐labeled cells become restricted around the Sox9‐positive cartilage anlage without themselves becoming Sox9‐positive. In the adult, the Prrx1eGFP transgene live labels a subpopulation of cells within the periosteum that are enriched at specific sites, and this population is diminished in aged mice. The green fluorescent protein (GFP)‐labeled subpopulation can be isolated using fluorescence‐activated cell sorting (FACS) and represents approximately 8% of all isolated periosteal cells. The GFP‐labeled subpopulation is significantly more osteogenic than unlabeled, GFP‐negative periosteal cells. In addition, the osteogenic and chondrogenic capacity of periosteal cells in vitro can be extended with the addition of fibroblast growth factor (FGF) to the expansion media. We provide evidence to suggest that osteoblasts contributing to cortical bone formation in the embryo originate from Prrx1eGFP‐positive cells within the perichondrium, which possibly piggyback on invading vascular cells and secrete new bone matrix. In summary, the Prrx1eGFP mouse is a powerful tool to visualize and isolate periosteal cells and to quantify their properties in the embryo and adult. © 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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影响因子:
2.1
作者:
Dwek, Jerry R.
通讯作者:
Dwek, Jerry R.
影响因子:
2.4
作者:
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通讯作者:
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DOI:
10.1073/pnas.0504750102
发表时间:
2005-10-11
影响因子:
11.1
作者:
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通讯作者:
de Crombrugghe, B
影响因子:
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作者:
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通讯作者:
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影响因子:
4.5
作者:
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通讯作者:
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