Monocyte chemotactic protein 3 is a homing factor for circulating angiogenic cells
Author(s) -
Mélanie Bousquenaud,
Chantal Schwartz,
Frédérique Léonard,
Magali Rolland-Turner,
Daniel Wagner,
Yvan Devaux
Publication year - 2012
Publication title -
cardiovascular research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.774
H-Index - 219
eISSN - 1755-3245
pISSN - 0008-6363
DOI - 10.1093/cvr/cvs140
Subject(s) - ccr1 , chemokine , monocyte , stromal cell , chemotaxis , stromal cell derived factor 1 , microbiology and biotechnology , angiogenesis , receptor , chemokine receptor , chemistry , immunology , medicine , cxcr4 , biology
Circulating angiogenic cells (CAC) participate in cardiac repair. CAC recruitment to the ischaemic heart is mainly induced by the chemokine (C-X-C motif) receptor 4 (CXCR4)/stromal-cell derived factor-1α axis. However, CAC mobilization is only partly prevented by CXCR4 blockade, indicating that other mechanisms are involved. Since the expression of monocyte chemotactic protein 3 (MCP3) is increased in ischaemic hearts, we hypothesized that it may participate in CAC mobilization.
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