CXCR4 and mobilization of hematopoietic precursors.

Abstract:

:The binding of the chemokine [C-X-C motif] ligand 12 (CXCL12 or stromal cell-derived factor 1alpha [SDF-1alpha]) constitutively produced by bone marrow stromal cells and osteoblasts, to the CXC receptor (CXCR) 4, a transmembrane chemokine receptor expressed on hematopoietic stem and progenitor cells (HSPCs), has emerged as a key signal for HSPC trafficking to and from the bone marrow. Disruption of CXCL12/CXCR4 signaling causes leukocytosis, with the release of HSPCs, neutrophils, and lymphocytes into the peripheral blood. Although mobilized peripheral blood has become the preferred source of stem cells for both autologous and allogeneic transplantation, the optimum strategy for obtaining mobilized products from donors is the subject of ongoing study. Granulocyte colony-stimulating factor (G-CSF) and plerixafor (AMD3100) are two agents used clinically to induce HSPC mobilization by disruption of the CXCL12/CXCR4 interaction. This chapter describes current procedures used to phenotypically and functionally characterize murine and human HSPCs mobilized by G-CSF or plerixafor.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Rettig MP,Ramirez P,Nervi B,DiPersio JF

doi

10.1016/S0076-6879(09)05203-3

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

57-90

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(09)05203-3

journal_volume

460

pub_type

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