The stromal cell-derived factor-1alpha/CXCR4 ligand-receptor axis is critical for progenitor survival and migration in the pancreas

J Cell Biol. 2003 Nov 24;163(4):859-69. doi: 10.1083/jcb.200304153.

Abstract

The SDF-1alpha/CXCR4 ligand/chemokine receptor pair is required for appropriate patterning during ontogeny and stimulates the growth and differentiation of critical cell types. Here, we demonstrate SDF-1alpha and CXCR4 expression in fetal pancreas. We have found that SDF-1alpha and its receptor CXCR4 are expressed in islets, also CXCR4 is expressed in and around the proliferating duct epithelium of the regenerating pancreas of the interferon (IFN) gamma-nonobese diabetic mouse. We show that SDF-1alpha stimulates the phosphorylation of Akt, mitogen-activated protein kinase, and Src in pancreatic duct cells. Furthermore, migration assays indicate a stimulatory effect of SDF-1alpha on ductal cell migration. Importantly, blocking the SDF-1alpha/CXCR4 axis in IFNgamma-nonobese diabetic mice resulted in diminished proliferation and increased apoptosis in the pancreatic ductal cells. Together, these data indicate that the SDF-1alpha-CXCR4 ligand receptor axis is an obligatory component in the maintenance of duct cell survival, proliferation, and migration during pancreatic regeneration.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cell Division / physiology
  • Cell Movement / physiology
  • Cell Survival / physiology
  • Cells, Cultured
  • Chemokine CXCL12
  • Chemokines, CXC / metabolism*
  • Disease Models, Animal
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Fetus
  • Ligands
  • Mice
  • Mice, Inbred NOD
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinases / metabolism
  • Pancreas / cytology
  • Pancreas / growth & development*
  • Pancreas / metabolism
  • Pancreatic Ducts / cytology
  • Pancreatic Ducts / growth & development
  • Pancreatic Ducts / metabolism
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Receptors, CXCR4 / metabolism*
  • Regeneration / physiology
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • src-Family Kinases / metabolism

Substances

  • Chemokine CXCL12
  • Chemokines, CXC
  • Cxcl12 protein, mouse
  • Ligands
  • Proto-Oncogene Proteins
  • Receptors, CXCR4
  • src-Family Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases