CXCR4 receptor expression on human retinal pigment epithelial cells from the blood-retina barrier leads to chemokine secretion and migration in response to stromal cell-derived factor 1 alpha

• Published in: The Journal of immunology (1950) 2000-10, Vol.165 (8), p.4372-4378
• Main Authors: Crane, I J, Wallace, C A, McKillop-Smith, S, Forrester, J V
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; blood-retina barrier; Blood-Retinal Barrier - immunology; Calcium Signaling - immunology; Cell Movement - immunology; Cells, Cultured; Chemokine CXCL12; Chemokines - biosynthesis; Chemokines - metabolism; Chemokines, CXC - biosynthesis; Chemokines, CXC - physiology; Child; Child, Preschool; CXCR4 protein; Female; Humans; Male; Pigment Epithelium of Eye - cytology; Pigment Epithelium of Eye - immunology; Pigment Epithelium of Eye - metabolism; Receptors, CXCR4 - biosynthesis; Receptors, CXCR4 - metabolism; stromal cell-derived factor 1^a; Stromal Cells - immunology; Tumor Cells, Cultured
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.165.8.4372

Retinal pigment epithelial (RPE) cells form part of the blood-retina barrier and have recently been shown to produce various chemokines in response to proinflammatory cytokines. As the scope of chemokine action has been shown to extend beyond the regulation of leukocyte migration, we have investigated the expression of chemokine receptors on RPE cells to determine whether they could be a target for chemokine signaling. RT-PCR analysis indicated that the predominant receptor expressed on RPE cells was CXCR4. The level of CXCR4 mRNA expression, but not cell surface expression, increased on stimulation with IL-1beta or TNF-alpha. CXCR4 protein could be detected on the surface of 16% of the RPE cells using flow cytometry. Calcium mobilization in response to the CXCR4 ligand stromal cell-derived factor 1alpha (SDF-1alpha) indicated that the CXCR4 receptors were functional. Incubation with SDF-1alpha resulted in secretion of monocyte chemoattractant protein-1, IL-8, and growth-related oncogene alpha. RPE cells also migrated in response to SDF-1alpha. As SDF-1alpha expression by RPE cells was detected constitutively, we postulate that SDF-1-CXCR4 interactions may modulate the affects of chronic inflammation and subretinal neovascularization at the RPE site of the blood-retina barrier.