1. Adrenomedullin in sinusoidal endothelial cells play protective roles against cold injury of liver.
- Author
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Iinuma N, Sakurai T, Kamiyoshi A, Ichikawa-Shindo Y, Arai T, Yoshizawa T, Koyama T, Uetake R, Kawate H, Muto S, Tagawa Y, Miyagawa S, and Shindo T
- Subjects
- Adrenomedullin metabolism, Animals, Apoptosis drug effects, Cell Adhesion, Cell Survival drug effects, Cells, Cultured, Cold Temperature, Flow Cytometry, Gene Expression Regulation drug effects, Intercellular Adhesion Molecule-1 genetics, Interleukin-1beta genetics, Interleukin-6 genetics, Liver cytology, Liver drug effects, Mice, Mice, Inbred C57BL, Receptors, Adrenomedullin, Receptors, Peptide metabolism, Reverse Transcriptase Polymerase Chain Reaction, Tumor Necrosis Factor-alpha genetics, Vascular Cell Adhesion Molecule-1 genetics, Adrenomedullin pharmacology, Adrenomedullin physiology, Liver metabolism
- Abstract
Donor organ damage caused by cold preservation is a major problem affecting liver transplantation. Cold preservation most easily damages liver sinusoidal endothelial cells (LSECs), and information about the molecules modulating LSECs function can provide the basis for new therapeutic strategies. Adrenomedullin (AM) is a peptide known to possess anti-apoptotic and anti-inflammatory properties. AM is abundant in vascular endothelial cells, but levels are comparatively low in liver, and little is known about its function there. In this study, we demonstrated both AM and its receptors are expressed in LSECs. AM treatment reduced LSECs loss and apoptosis under cold treatment. AM also downregulated cold-induced expression of TNFalpha, IL1beta, IL6, ICAM1 and VCAM1. AM reduced apoptosis and expression of ICAM1 and VCAM1 in an in vivo liver model subjected to cold storage. Conversely, apoptosis was exacerbated in livers from AM and RAMP2 (AM receptor activity-modifying protein) knockout mice. These results suggest that AM expressed in LSECs exerts a protective effect against cold-organ damage through modulation of apoptosis and inflammation., (Copyright (c) 2010 Elsevier Inc. All rights reserved.)
- Published
- 2010
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