Therapeutic targeting of a stem cell niche

被引:0
|
作者
Gregor B Adams
Roderick P Martin
Ian R Alley
Karissa T Chabner
Kenneth S Cohen
Laura M Calvi
Henry M Kronenberg
David T Scadden
机构
[1] Center for Regenerative Medicine,Department of Medicine
[2] Massachusetts General Hospital,undefined
[3] Harvard Medical School,undefined
[4] Endocrine Unit,undefined
[5] Massachusetts General Hospital,undefined
[6] Harvard Medical School,undefined
[7] Endocrine Unit,undefined
[8] University of Rochester School of Medicine,undefined
[9] Harvard Stem Cell Institute,undefined
[10] Harvard University,undefined
来源
Nature Biotechnology | 2007年 / 25卷
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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 number1,2,3. 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.
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页码:238 / 243
页数:5
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