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Alternate splicing of mouse fusin/CXC chemokine receptor-4: stromal cell-derived factor-1α is a ligand for both CXC chemokine receptor-4 isoforms

Authors

  • M. Heesen
  • M.A. Berman
  • U.E. Höpken
  • N.P. Gerard
  • M.E. Dorf

Journal

  • Journal of Immunology

Citation

  • J Immunol 158 (8): 3561-3564

Abstract

  • Inspection of the intron splice junction of the mouse chemokine receptor fusin/CXC chemokine receptor R-4 (CXCR-4) revealed a potential in-frame alternative splice site in the region encoding the N-terminal ectodomain of the receptor. Both predicted splice products were detected by reverse transcriptase-PCR. Cell lines of T lymphocyte, B lymphocyte, and macrophage lineage, plus populations of elicited peritoneal exudate cells, thymocytes, and astrocytes coexpressed mRNA for both isoforms. The full length cDNA of the shorter alternate splice product, termed CXCR-4B, was cloned from peritoneal exudate cell RNA. Chinese hamster ovary cells transfected with either isoform, CXCR-4A or CXCR-4B, responded to stromal cell-derived factor-1{alpha} with a rise in intracellular calcium. Both alternate splice products are therefore functional stromal cell-derived factor-1 {alpha} receptors.


DOI

doi:content/158/8/3561