Age-associated declining of the regeneration potential of skeletal stem/progenitor cells

被引:3
|
作者
Mancinelli, Luigi [1 ,2 ]
Intini, Giuseppe [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Dept Periodont & Prevent Dent, Sch Dent Med, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Ctr Craniofacial Regenerat, Sch Dent Med, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Med Hematol Oncol, Sch Med, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, UPMC Hillman Canc Ctr, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
skeletal stem/progenitor cells (SSPCs); aging; bone regeneration; Prrx1/Prx1; senescence; MESENCHYMAL STROMAL CELLS; STEM-CELL; BONE-MARROW; IDENTIFICATION; SENESCENCE; SPECIFICATION; QUIESCENCE; PERIOSTEUM; TELOMERES; CARTILAGE;
D O I
10.3389/fphys.2023.1087254
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bone fractures represent a significant health burden worldwide, mainly because of the rising number of elderly people. As people become older, the risk and the frequency of bone fractures increase drastically. Such increase arises from loss of skeletal integrity and is also associated to a reduction of the bone regeneration potential. Central to loss of skeletal integrity and reduction of regeneration potential are the skeletal stem/progenitor cells (SSPCs), as they are responsible for the growth, regeneration, and repair of the bone tissue. However, the exact identity of the SSPCs has not yet been determined. Consequently, their functions, and especially dysfunctions, during aging have never been fully characterized. In this review, with the final goal of describing SSPCs dysfunctions associated to aging, we first discuss some of the most recent findings about their identification. Then, we focus on how SSPCs participate in the normal bone regeneration process and how aging can modify their regeneration potential, ultimately leading to age-associated bone fractures and lack of repair. Novel perspectives based on our experience are also provided.
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页数:10
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