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PMID: 10550315 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Stromal-cell derived factor is expressed by dendritic cells and endothelium in human skin.

The American journal of pathology ·Vol. 155 ·No. 5 ·1999-11-00 ·Pages 1577-86

Pablos JL, Amara A, Bouloc A, Santiago B, Caruz A, Galindo M, Delaunay T, Virelizier JL, Arenzana-Seisdedos F

Abstract

Stromal-cell derived factor or SDF-1 is a CXC chemokine constitutively expressed by stromal bone marrow cell cultures that binds to the G-protein-coupled receptor CXCR4. SDF-1/CXCR4 represents a unique, nonpromiscuous ligand/receptor pair that plays an essential role in prenatal myelo- and lymphopoiesis as well as in cardiovascular and neural development. SDF-1 prevents entry of CXCR4-dependent (X4) HIV viruses in T lymphocytes, by binding and internalizing CXCR4. The expression pattern of SDF-1 protein in normal tissues is not known. Here we describe an analysis of SDF-1 mRNA and protein in normal and inflamed skin by in situ hybridization and immunohistochemistry, using a novel anti-SDF-1 monoclonal antibody. We also describe the expression pattern of CXCR4 receptor by immunohistochemistry. Our results show that SDF-1 protein and mRNA are normally expressed by endothelial cells, pericytes, and either resident or explanted CD1a+ dendritic cells. Epithelial cells of sweat glands but not keratinocytes also express SDF-1. In various inflammatory skin diseases, a large number of mononuclear cells and fibroblasts in close contact with CXCR4-positive lymphocytic infiltrates also express SDF-1. CXCR4 was also detected in many different normal cell types, including endothelial and epithelial cells, which points to a role for SDF-1/CXCR4 cell signaling in vascular and epithelial homeostasis. The demonstration of SDF-1 expression in dendritic and endothelial cells provides new insights into the mechanisms of normal and pathological lymphocyte circulation and makes it possible to envisage a role for locally secreted SDF-1 in the selective incapacity of mucosal dendritic cells to support and propagate infection by X4 HIV isolates.

MeSH Terms
Chemokine CXCL12 Chemokines, CXC/biosynthesis Dendritic Cells/metabolism Endothelium, Vascular/metabolism Humans Immunohistochemistry Microcirculation Microscopy, Confocal Pericytes/metabolism Receptors, CXCR4/biosynthesis Skin/blood supply,metabolism,pathology
Chemicals
CXCL12 protein, human Chemokine CXCL12 Chemokines, CXC Receptors, CXCR4
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Pablos J L
Servicio de Reumatología, Centro de Investigación, Hospital 12 de Octubre, Madrid, Spain. [email protected]
Amara A
Bouloc A
Santiago B
Caruz A
Galindo M
Delaunay T
Virelizier J L
Arenzana-Seisdedos F
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Article Info
Journal
The American journal of pathology
Abbr.
Am J Pathol
ISSN
0002-9440
Published
1999-11-00
Pages
1577-86
Language
English
Region
United States
NLM ID
0370502
PMCID
PMC1866989
Subset
IM
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