Source:http://linkedlifedata.com/resource/pubmed/id/20524780
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-7-12
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pubmed:abstractText |
Endothelial progenitor cell (EPC) therapy represents a novel strategy for a variety of diseases. Interestingly, spleen acts an important reservoir during EPC trafficking. Therefore, we investigated the involvement of stromal cell-derived factor-1 (SDF-1)/CXCR4 in EPC settlement in the spleen. EPC were cultured and characterized as previous methods. Then, 1 x 10(6) EPC were labeled with DiI-LDL and intravenously infused into C57/BL6 mice. Immunohistochemical staining showed homing of transplanted EPC in the spleen 24 h later, indicating recruitment of transplanted EPC into the spleen. The distribution of EPC in different organs was evaluated by fluorescence-activated cell sorting of Sca-1/Flk-1(+) cells, which demonstrated settlement of EPC in the spleen. Removal of the splenic niche by splenectomy augmented circulating EPC 12 and 24 h later, indicating an important role of spleen on modulation of EPC-circulating dynamics. Expressions of SDF-1 in the spleen and CXCR4 in EPC were revealed by enzyme-linked immunosorbent assay (ELISA) and reverse transcription polymerase chain reaction (RT-PCR). A modified Boyden chamber assay showed that SDF-1 (10 or 100 ng/mL) induced EPC migration in vitro. Injection of the SDF-1 protein into the spleen increased the number of splenic EPC. In contrast, injection of a SDF-1 antibody or AMD3100 (SDF-1/CXCR4 axis antagonist) attenuated their settlement and did not induce EPC apoptosis. These results indicate that the SDF-1/CXCR4 axis is involved in recruitment of EPC to the spleen, and enhances our understanding of EPC-circulating kinetics.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1532-4281
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
246-54
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pubmed:meshHeading |
pubmed-meshheading:20524780-Animals,
pubmed-meshheading:20524780-Apoptosis,
pubmed-meshheading:20524780-Bone Marrow Cells,
pubmed-meshheading:20524780-Cell Movement,
pubmed-meshheading:20524780-Cells, Cultured,
pubmed-meshheading:20524780-Chemokine CXCL12,
pubmed-meshheading:20524780-Endothelial Cells,
pubmed-meshheading:20524780-Female,
pubmed-meshheading:20524780-Mice,
pubmed-meshheading:20524780-Mice, Inbred C57BL,
pubmed-meshheading:20524780-Receptors, CXCR4,
pubmed-meshheading:20524780-Spleen,
pubmed-meshheading:20524780-Splenectomy,
pubmed-meshheading:20524780-Stem Cells
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pubmed:year |
2010
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pubmed:articleTitle |
The spleen recruits endothelial progenitor cell via SDF-1/CXCR4 axis in mice.
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pubmed:affiliation |
Department of Cardiology, XinQiao Hospital, ChongQing, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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