Expression of vascular cell adhesion molecule-1 in fibroblastlike synoviocytes after stimulation with tumor necrosis factor.

CW Marlor, DL Webb, MP Bombara… - The American journal …, 1992 - ncbi.nlm.nih.gov
CW Marlor, DL Webb, MP Bombara, JM Greve, ML Blue
The American journal of pathology, 1992ncbi.nlm.nih.gov
Rapid expression of mRNA encoding vascular cell adhesion molecule-1 (VCAM-1) was
induced by tumor necrosis factor (TNF) in fibroblast-like cells obtained from synovial tissue.
Both alternatively spliced forms of VCAM-1 mRNA were detected by polymerase chain
reaction in TNF-stimulated fibroblast-like synoviocytes. Western blotting analysis showed
that two distinct proteins, reactive with an anti-VCAM-1 anti-sera, were expressed by 2 hours
of TNF stimulation in both synoviocytes and human umbilical cord vein endothelial cells …
Abstract
Rapid expression of mRNA encoding vascular cell adhesion molecule-1 (VCAM-1) was induced by tumor necrosis factor (TNF) in fibroblast-like cells obtained from synovial tissue. Both alternatively spliced forms of VCAM-1 mRNA were detected by polymerase chain reaction in TNF-stimulated fibroblast-like synoviocytes. Western blotting analysis showed that two distinct proteins, reactive with an anti-VCAM-1 anti-sera, were expressed by 2 hours of TNF stimulation in both synoviocytes and human umbilical cord vein endothelial cells (HUVEC). The majority of HUVEC and synoviocytes displayed VCAM-1 surface expression after several hours of TNF stimulation. In contrast, dermal fibroblasts upregulated intercellular adhesion molecule-1 (ICAM-1) but not VCAM-1 expression in response to TNF. These results indicate that VCAM-1 and ICAM-1 expression can be differentially regulated and suggest tissue specific regulation of VCAM-1 expression. Furthermore, these findings may provide an explanation for the chronic retention and activation of long-lived lymphocytes and monocytes, which express VLA-4 (the receptor for VCAM-1), in the synovium in rheumatoid arthritis.
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