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The Many Facets of SDF-1α, CXCR4 Agonists and Antagonists on Hematopoietic Progenitor Cells
Author(s) -
Anne Faber,
Christoph Roderburg,
Frederik Wein,
Rainer Saffrich,
Anja Seckinger,
Kerstin Horsch,
Anke Diehlmann,
Donald Wong,
Gary Bridger,
Volker Eckstein,
Anthony D. Ho,
Wolfgang Wagner
Publication year - 2007
Publication title -
journal of biomedicine and biotechnology
Language(s) - English
Resource type - Journals
eISSN - 1110-7251
pISSN - 1110-7243
DOI - 10.1155/2007/26065
Subject(s) - stromal cell , cxcr4 , progenitor cell , cd34 , agonist , chemotaxis , antagonist , chemistry , microbiology and biotechnology , receptor , stem cell , biology , cancer research , biochemistry , chemokine
Stromal cell-derived factor-1alpha (SDF-1α) has pleiotropic effects on hematopoietic progenitor cells (HPCs). We have monitored podia formation, migration, proliferation, and cell-cell adhesion of human HPC under the influence of SDF-1α, a peptide agonist of CXCR4 (CTCE-0214), a peptide antagonist (CTCE-9908), and a nonpeptide antagonist (AMD3100). Whereas SDF-1α induced migration of CD34+ cells in a dose-dependent manner, CTCE-0214, CTCE-9908, and AMD3100 did not induce chemotaxis in this concentration range albeit the peptides CTCE-0214 and CTCE-9908 increased podia formation. Cell-cell adhesion of HPC to human mesenchymal stromal cells was impaired by the addition of SDF-1α, CTCE-0214, and AMD3100. Proliferation was not affected by SDF-1α or its analogs. Surface antigen detection of CXCR4 was reduced upon treatment with SDF-1α or AMD3100 and it was enhanced by CTCE-9908. Despite the fact that all these molecules target the same CXCR4 receptor, CXCR4 agonists and antagonists have selective effects on different functions of the natural molecule

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