Bone marrow stem cells: current and emerging concepts

被引:57
作者
Mendez-Ferrer, Simon [1 ]
Scadden, David T. [2 ,3 ,4 ]
Sanchez-Aguilera, Abel [1 ]
机构
[1] CNIC, Stem Cell Niche Pathophysiol Grp, Madrid, Spain
[2] Harvard Univ, Stem Cell & Regenerat Biol Dept, Cambridge, MA 02138 USA
[3] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[4] Harvard Stem Cell Inst, Cambridge, MA USA
来源
MARROW | 2015年 / 1335卷
关键词
mesenchymal stem/stromal cells; hematopoietic stem cells; bone marrow stem cell niche; hierarchical crosstalk; HEMATOPOIETIC STEM; PROGENITOR CELLS; CD34; EXPRESSION; FACTOR-I; QUIESCENCE; MICE; DIFFERENTIATION; ENGRAFTMENT; OSTEOBLAST; NICHES;
D O I
10.1111/nyas.12641
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The interactions of stromal cells with hematopoietic cells in the bone marrow have long been a subject of research, but only recently have technologies allowed us to dissect them at the stem cell level. On the other hand, limitations of these technical tools might explain numerous discrepancies in this field. It is becoming increasingly clear that mesenchymal stem cells (MSCs) represent an important component of the hematopoietic stem cell (HSC) niche in the bone marrow. However, there is heterogeneity among HSCs, and many putatively different mesenchymal progenitors identified in the bone marrow using Cre recombinase-driven mouse lines seem to exhibit HSC niche properties. Development of better reporter lines has demonstrated that some of these Cre lines do not always specifically mark the expected cells. Also, characterization of different cell populations has often been partial, and issues of redundancy and compensation might explain apparently contradictory results. Recognizing and overcoming these limitations, while also clearly defining the distinctions between subgroups of mesenchymal cells, will be essential to advance the field.
引用
收藏
页码:32 / 44
页数:13
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