Pathways implicated in stem cell migration: the SDF-1/CXCR4 axis

Methods Mol Biol. 2011:750:277-89. doi: 10.1007/978-1-61779-145-1_19.

Abstract

The hallmark of hematopoietic stem and progenitor cells (HSPCs) is their motility, which is essential for their function, such as recruitment upon demand. Stromal Derived Factor-1 (SDF-1, CXCL12) and its major receptor CXCR4 play major roles in stem cell motility and development. In vitro migration assays, implicating either gradients or cell surface-bound forms of SDF-1, are easy to perform and provide vital information regarding directional and random stem cell motility, which correlate with their repopulation potential in clinical and experimental transplantations. In vivo stem cell homing to the bone marrow, their retention, engraftment, and egress to the circulation, all involve SDF-1/CXCR4 interactions. Finally, other stem cell features such as stem cell survival and proliferation, are also dependent on the SDF-1/CXCR4 axis.

MeSH terms

  • Animals
  • Antigens, CD34 / analysis
  • Antigens, CD34 / immunology
  • Bone Marrow / immunology
  • Bone Marrow / metabolism*
  • Cell Adhesion
  • Cell Count
  • Cell Migration Assays
  • Cell Movement*
  • Cell Survival
  • Cells, Cultured
  • Chemokine CXCL12 / immunology
  • Chemokine CXCL12 / metabolism*
  • Chemotaxis / physiology*
  • Colony-Forming Units Assay
  • Flow Cytometry
  • Graft Survival / immunology
  • Hematopoietic Stem Cell Mobilization
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / physiology
  • Humans
  • Mice
  • Receptors, CXCR4 / immunology
  • Receptors, CXCR4 / metabolism*
  • Whole-Body Irradiation

Substances

  • Antigens, CD34
  • Chemokine CXCL12
  • Receptors, CXCR4