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Transendothelial Migration of Hematopoietic Progenitor Cells
Author(s) -
MÖHLE ROBERT,
BAUTZ FRANK,
DENZLINGER CLAUDIO,
KANZ LOTHAR
Publication year - 2001
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1111/j.1749-6632.2001.tb03571.x
Subject(s) - microbiology and biotechnology , homing (biology) , chemotaxis , receptor , progenitor cell , chemokine receptor , biology , haematopoiesis , stromal cell , chemokine , stem cell , cannabinoid receptor type 2 , chemistry , cancer research , cannabinoid receptor , biochemistry , ecology , agonist
A bstract : There is increasing evidence that hematopoietic stem cell mobilization and homing is regulated not only by adhesion molecules and cytokines, but also by chemotactic factors that support transendothelial migration across the bone marrow sinusoidal endothelium. Many receptors for chemotactic mediators belong to the family of G protein‐coupled seven‐transmembrane receptors (7‐TMR). Signaling via G proteins, particularly G i proteins, results in a chemotactic response of the cells towards a gradient of the corresponding ligand. Recent studies have provided evidence for expression of several 7‐TMR on immature hematopoietic progenitor cells, which potentially mediate chemotactic effects: chemokine receptors (e.g., CXCR4, receptor for stromal cell‐derived factor‐1), receptors for lipid mediators (e.g., the cysteinyl leukotriene receptor cysLT1 and the peripheral cannabinoid receptor cb2), and receptors for neuroendocrine hormones (e.g., the somatostatin receptor sst2). From these studies it can be concluded that migration of hematopoietic progenitor and stem cells is controlled by a variety of chemotactic factors rather than by a single chemokine (e.g., SDF‐1). Trafficking of immature hematopoietic cells may require combined and interactive regulatory functions of these mediators.