Proteoglycans guide SDF-1-induced migration of hematopoietic progenitor cells

J Leukoc Biol. 2002 Aug;72(2):353-62.

Abstract

Stromal cell-derived factor-1 (SDF-1) is a chemoattractant involved in hematopoietic progenitor cell (HPC) trafficking to the bone marrow. We studied the role of bone marrow endothelial proteoglycans (PGs) in SDF-1-mediated migration of HPC using a transwell assay. A subclone of progenitor cell line KG-1 (KG-1v) was used, displaying CXCR4-dependent transmigration. Cell surface PGs on bone marrow endothelial cell line 4LHBMEC did not mediate SDF-1-induced transendothelial migration. In contrast, transwell filters precoated with various glycosaminoglycans (GAGs) enhanced migration toward SDF-1. SDF-1-induced migration was reduced by degradation of heparan sulfate in subendothelial matrix produced by 4LHBMEC. The stimulating effect of GAGs was caused by the formation of a stable haptotactic SDF-1 gradient, as SDF-1 bound to immobilized GAGs and triggered migration. Soluble heparan sulfate enhanced SDF-1-induced migration dose-dependently, suggesting that SDF-1-heparan sulfate complexes optimized SDF-1 presentation. In conclusion, we provide evidence that PGs in the subendothelial matrix establish an SDF-1 gradient guiding migrating HPC into the bone marrow.

MeSH terms

  • Bone Marrow / blood supply
  • Bone Marrow / chemistry*
  • Cell Adhesion / drug effects
  • Cell Movement / drug effects
  • Cells, Cultured / drug effects
  • Chemokine CXCL12
  • Chemokines, CXC / administration & dosage
  • Chemokines, CXC / chemistry
  • Chemokines, CXC / pharmacology*
  • Dose-Response Relationship, Drug
  • Endothelium, Vascular / chemistry
  • Endothelium, Vascular / cytology
  • Extracellular Matrix / chemistry
  • Fibronectins / metabolism
  • Fibronectins / pharmacology
  • HL-60 Cells / drug effects
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects*
  • Heparin / chemistry
  • Heparin / pharmacology
  • Heparitin Sulfate / chemistry
  • Heparitin Sulfate / pharmacology
  • Humans
  • Macromolecular Substances
  • Osmolar Concentration
  • Protein Binding
  • Proteoglycans / chemistry
  • Proteoglycans / pharmacology*
  • Proteoglycans / physiology
  • Receptors, CXCR4 / drug effects
  • Receptors, CXCR4 / metabolism
  • Solubility
  • Structure-Activity Relationship
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Vascular Cell Adhesion Molecule-1 / pharmacology

Substances

  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines, CXC
  • Fibronectins
  • Macromolecular Substances
  • Proteoglycans
  • Receptors, CXCR4
  • Vascular Cell Adhesion Molecule-1
  • Heparin
  • Heparitin Sulfate