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Induction of the chemokine stromal-derived factor-1 following DNA damage improves human stem cell function
Tanya Ponomaryov, … , Dov Zipori, Tsvee Lapidot
Tanya Ponomaryov, … , Dov Zipori, Tsvee Lapidot
Published December 1, 2000
Citation Information: J Clin Invest. 2000;106(11):1331-1339. https://doi.org/10.1172/JCI10329.
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Article

Induction of the chemokine stromal-derived factor-1 following DNA damage improves human stem cell function

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Abstract

The chemokine stromal-derived factor-1 (SDF-1) controls many aspects of stem cell function. Details of its regulation and sites of production are currently unknown. We report that in the bone marrow, SDF-1 is produced mainly by immature osteoblasts and endothelial cells. Conditioning with DNA-damaging agents (ionizing irradiation, cyclophosphamide, and 5-fluorouracil) caused an increase in SDF-1 expression and in CXCR4-dependent homing and repopulation by human stem cells transplanted into NOD/SCID mice. Our findings suggest that immature osteoblasts and endothelial cells control stem cell homing, retention, and repopulation by secreting SDF-1, which also participates in host defense responses to DNA damage.

Authors

Tanya Ponomaryov, Amnon Peled, Isabelle Petit, Russell S. Taichman, Liliana Habler, Judith Sandbank, Fernando Arenzana-Seisdedos, Aude Magerus, Antonio Caruz, Nobutaka Fujii, Arnon Nagler, Meir Lahav, Martin Szyper-Kravitz, Dov Zipori, Tsvee Lapidot

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Figure 4

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Increased levels of SDF-1 in the spleen of NOD/SCID after TBI. (a) SDF-1...
Increased levels of SDF-1 in the spleen of NOD/SCID after TBI. (a) SDF-1 mRNA in the BM and spleen from the same mouse per time point. (b) Semisolid colony assay for migrating progenitors to spleen CM collected before, 24 hours, or 48 hours after TBI with and without anti-CXCR4 Ab pretreatment.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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