Therapeutic targeting of a stem cell niche

被引:220
作者
Adams, Gregor B.
Martin, Roderick P.
Alley, Ian R.
Chabner, Karissa T.
Cohen, Kenneth S.
Calvi, Laura M.
Kronenberg, Henry M.
Scadden, David T.
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Endocrine Unit, Boston, MA 02114 USA
[3] Univ Rochester, Sch Med, Rochester, NY 14642 USA
[4] Harvard Univ, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
关键词
D O I
10.1038/nbt1281
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The specialized microenvironment or niche where stem cells reside provides regulatory input governing stem cell function. We tested the hypothesis that targeting the niche might improve stem cell-based therapies using three mouse models that are relevant to clinical uses of hematopoietic stem ( HS) cells. We and others previously identified the osteoblast as a component of the adult HS cell niche and established that activation of the parathyroid hormone ( PTH) receptor on osteoblasts increases stem cell number(1-3). Here we show that pharmacologic use of PTH increases the number of HS cells mobilized into the peripheral blood for stem cell harvests, protects stem cells from repeated exposure to cytotoxic chemotherapy and expands stem cells in transplant recipients. These data provide evidence that the niche may be an attractive target for drug-based stem cell therapeutics.
引用
收藏
页码:238 / 243
页数:6
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