Cyclosporine A enhances leukocyte binding by human intestinal microvascular endothelial cells through inhibition of p38 MAPK and iNOS. Paradoxical proinflammatory effect on the microvascular endothelium

• Published in: The Journal of biological chemistry 2002-09, Vol.277 (38), p.35605-35615
• Main Authors: Rafiee, Parvaneh, Johnson, Christopher P, Li, Mona S, Ogawa, Hitoshi, Heidemann, Jan, Fisher, Pamela J, Lamirand, Thomas H, Otterson, Mary F, Wilson, Keith T, Binion, David G
• Format: Article
• Language: English
• Subjects: Base Sequence; Cell Adhesion - drug effects; Cells, Cultured; Cyclosporine - pharmacology; DNA Primers; Endothelium, Vascular - cytology; Endothelium, Vascular - drug effects; Endothelium, Vascular - enzymology; Endothelium, Vascular - metabolism; Humans; Immunosuppressive Agents - pharmacology; Intestines - blood supply; Leukocytes - cytology; Leukocytes - drug effects; Lipopolysaccharides - pharmacology; Mitogen-Activated Protein Kinases - antagonists & inhibitors; NF-kappa B - metabolism; Nitric Oxide - biosynthesis; Nitric Oxide Synthase - antagonists & inhibitors; Nitric Oxide Synthase Type II; p38 Mitogen-Activated Protein Kinases; Signal Transduction - drug effects; Tumor Necrosis Factor-alpha - physiology
• ISSN: 0021-9258
• DOI: 10.1074/jbc.M205826200

The calcineurin inhibitor cyclosporine A (CsA) modulates leukocyte cytokine production but may also effect nonimmune cells, including microvascular endothelial cells, which regulate the inflammatory process through leukocyte recruitment. We hypothesized that CsA would promote a proinflammatory phenotype in human intestinal microvascular endothelial cells (HIMEC), by inhibiting inducible nitric-oxide synthase (iNOS, NOS2)-derived NO, normally an important mechanism in limiting endothelial activation and leukocyte adhesion. Primary cultures of HIMEC were used to assess CsA effects on endothelial activation, leukocyte interaction, and the expression of iNOS as well as cell adhesion molecules. CsA significantly increased leukocyte binding to activated HIMEC, but paradoxically decreased endothelial expression of cell adhesion molecules (E-selectin, intercellular adhesion molecule 1, and vascular cell adhesion molecule-1). In contrast, CsA completely inhibited the expression of iNOS in tumor necrosis factor-alpha/lipopolysaccharide-activated HIMEC. CsA blocked p38 MAPK phosphorylation in activated HIMEC, a key pathway in iNOS expression, but failed to inhibit NFkappaB activation. These studies demonstrate that CsA exerts a proinflammatory effect on HIMEC by blocking iNOS expression. CsA exerts a proinflammatory effect on the microvascular endothelium, and this drug-induced endothelial dysfunction may help explain its lack of efficacy in the long-term treatment of chronically active inflammatory bowel disease.