Local signals in stem cell-based bone marrow regeneration

被引:52
作者
Han, W [1 ]
Yu, Y
Liu, XY
机构
[1] Shanghai Jiao Tong Univ, Stem Cell Res Ctr, Sch Pharm, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Municipal Key Lab Vet Biotechnol, Shanghai 200030, Peoples R China
[3] Zhejiang Univ Technol & Sci, Xinyuan Inst Med & Biotechnol, Sch Life Sci, Hangzhou 310018, Peoples R China
关键词
bone marrow; regeneration; hematopoietic stem cells; mesenchymal stem cells; signaling molecules; myelosuppression;
D O I
10.1038/sj.cr.7310026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cellular basis of bone marrow (BM) tissue development and regeneration is mediated through hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCS). Local interplays between hematopoietic cells and BM stromal cells (BMSCs) determine the reconstitution of hematopoiesis after myelosuppression. Here we review the BM local signals in control of BM regeneration after insults. Hematopoietic growth factors (HGFs) and cytokines produced by BMSCs are primary factors in regulation of BM hematopoiesis. Morphogens which are critical to early embryo development in multiple species have been added to the family of HSCs regulators, including families of Writ proteins, Notch ligands, BMPs, and Hedgehogs. Global gene expression analysis of HSCs and BMSCs has begun to reveal signature groups of genes for both cell types. More importantly, analysis of global gene expression coupled with biochemical and biological studies of local signals during BM regeneration have strongly suggested that HGFs and cytokines may not be the primary local regulators for BM recovery, rather chemokines (SDF-1, FGF-4) and angiogenic growth factors (VEGF-A, Ang-1) play instructive roles in BM reconstitution after myelosuppression. A new direction of management of BM toxicity is emerging from the identification of BM regenerative regulators.
引用
收藏
页码:189 / 195
页数:7
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