α-Melanocyte Stimulating Hormone Prevents Lipopolysaccharide-Induced Vasculitis by Down-Regulating Endothelial Cell Adhesion Molecule Expression

• Published in: Endocrinology (Philadelphia) 2003-01, Vol.144 (1), p.360-370
• Main Authors: Scholzen, T. E, Sunderkötter, C, Kalden, D.-H, Brzoska, T, Fastrich, M, Fisbeck, T, Armstrong, C. A, Ansel, J. C, Luger, T. A
• Format: Article
• Language: English
• Subjects: Adhesion; alpha-MSH - pharmacology; Animals; Biological and medical sciences; Cardiovascular system; Cell activation; Cell Adhesion; Cell adhesion & migration; Cell adhesion molecules; Cells, Cultured; Damage; Diapedesis; E-selectin; E-Selectin - genetics; Endothelial cells; Endothelium, Vascular - metabolism; Enzyme-Linked Immunosorbent Assay; Female; Flow Cytometry; Gene expression; Gene Expression Regulation - drug effects; Hemorrhage; Humans; Inflammatory diseases; Intercellular adhesion molecule 1; Intercellular Adhesion Molecule-1 - genetics; Leukocytes; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Lymphocytes; Lymphocytes - physiology; Male; Medical sciences; Mice; Mice, Inbred BALB C; Microcirculation; Microvasculature; Miscellaneous; NF-kappa B - physiology; Pharmacology. Drug treatments; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - analysis; Sepsis; Shwartzman reaction; Transcription activation; Tumor Necrosis Factor-alpha - pharmacology; Tumor necrosis factor-α; Vascular cell adhesion molecule 1; Vascular Cell Adhesion Molecule-1 - genetics; Vasculitis; Vasculitis - chemically induced; Vasculitis - prevention & control
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2002-220651

The neuroendocrine hormone α-melanocyte stimulating hormone (MSH) has profound antiinflammatory and immunomodulating properties. Here we have examined the possibility that α-MSH may interfere with the expression and function of cell adhesion molecules (CAMs) expressed by human dermal microvascular endothelial cells (HDMECs) in response to lipopolysaccharide (LPS) or TNFα in vitro and in vivo. In HDMEC, α-MSH (10−8/10−12 m) profoundly reduced the mRNA and protein expression of E-selectin, vascular CAM (VCAM)-1, and intercellular CAM (ICAM)-1 induced by LPS or TNFα as determined by semiquantitative RT-PCR, ELISA, and fluorescence-activated cell sorter analysis. In addition, α-MSH significantly impaired the LPS-induced ICAM-1 and VCAM-1-mediated adhesion of lymphocytes to HDMEC monolayer in a functional adhesion assay. Likewise, α-MSH effectively inhibited the transcription factor nuclear factor-κB activation in HDMEC, which is required for CAM gene expression. Importantly in vivo, in murine LPS-induced cutaneous vasculitis (local Shwartzman reaction), a single ip injection of α-MSH significantly suppressed the deleterious vascular damage and hemorrhage by inhibiting the sustained expression of vascular E-selectin and VCAM-1. This persistent expression has been implicated in the dysregulation of diapedesis and activation of leukocytes, which subsequently leads to hemorrhagic vascular damage. Our findings indicate that α-MSH may have an important therapeutical potential for the treatment of vasculitis, sepsis, and inflammatory diseases.