1. Academic Validation
  2. The many facets of SDF-1alpha, CXCR4 agonists and antagonists on hematopoietic progenitor cells

The many facets of SDF-1alpha, CXCR4 agonists and antagonists on hematopoietic progenitor cells

  • J Biomed Biotechnol. 2007;2007(3):26065. doi: 10.1155/2007/26065.
Anne Faber 1 Christoph Roderburg Frederik Wein Rainer Saffrich Anja Seckinger Kerstin Horsch Anke Diehlmann Donald Wong Gary Bridger Volker Eckstein Anthony D Ho Wolfgang Wagner
Affiliations

Affiliation

  • 1 Department of Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
Abstract

Stromal cell-derived factor-1alpha (SDF-1alpha) 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-1alpha, a peptide agonist of CXCR4 (CTCE-0214), a peptide antagonist (CTCE-9908), and a nonpeptide antagonist (AMD3100). Whereas SDF-1alpha 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-1alpha, CTCE-0214, and AMD3100. Proliferation was not affected by SDF-1alpha or its analogs. Surface antigen detection of CXCR4 was reduced upon treatment with SDF-1alpha 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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