In Osteoporosis, differentiation of mesenchymal stem cells (MSCs) improves bone marrow adipogenesis

被引:167
作者
Maria Pino, Ana [1 ]
Rosen, Clifford J. [2 ]
Pablo Rodriguez, J. [1 ]
机构
[1] Univ Chile, Lab Biol Celular & Mol, INTA, Santiago, Chile
[2] Maine Med Ctr, Res Inst, Scarborough, ME USA
关键词
MSCs; osteoporosis; adipogenesis; bone marrow microenvironment; SUPPRESSES OSTEOGENIC DIFFERENTIATION; GROWTH-FACTOR-I; GENE-EXPRESSION; STROMAL CELLS; SELF-RENEWAL; OSTEOBLAST DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; PROMOTES PROLIFERATION; ADIPOSE-TISSUE; FAT-CONTENT;
D O I
10.4067/S0716-97602012000300009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The formation, maintenance, and repair of bone tissue involve close interlinks between two stem cell types housed in the bone marrow: the hematologic stem cell originating osteoclasts and mesenchymal stromal cells (MSCs) generating osteoblasts. In this review, we consider malfunctioning of MSCs as essential for osteoporosis. In osteoporosis, increased bone fragility and susceptibility to fractures result from increased osteoclastogenesis and insufficient osteoblastogenesis. MSCs are the common precursors for both osteoblasts and adipocytes, among other cell types. MSCs commitment towards either the osteoblast or adipocyte lineages depends on suitable regulatory factors activating lineage-specific transcriptional regulators. In osteoporosis, the reciprocal balance between the two differentiation pathways is altered, facilitating adipose accretion in bone marrow at the expense of osteoblast formation; suggesting that under this condition MSCs activity and their microenvironment may be disturbed. We summarize research on the properties of MSCs isolated from the bone marrow of control and osteoporotic post-menopausal women. Our observations indicate that intrinsic properties of MSCs are disturbed in osteoporosis. Moreover, we found that the regulatory conditions in the bone marrow fluid of control and osteoporotic patients are significantly different. These conclusions should be relevant for the use of MSCs in therapeutic applications.
引用
收藏
页码:279 / 287
页数:9
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