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Lipid peroxidation‐induced VEGF expression in the skin of KK A y obese mice
Author(s) -
Nakai Kozo,
Yoneda Kozo,
Ishihara Yasuhiro,
Ohmori Koji,
Moriue Tetsuya,
Igarashi Junsuke,
Kohno Masakazu,
Kosaka Hiroaki,
Kubota Yasuo
Publication year - 2011
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2010.01223.x
Subject(s) - lipid peroxidation , endocrinology , medicine , cd36 , hacat , mapk/erk pathway , chemistry , vascular endothelial growth factor , oxidative stress , biology , biochemistry , kinase , in vitro , receptor , vegf receptors
Obesity is known to be associated with a number of effects on skin physiology. KK A y obese mouse is a model of type 2 diabetes characterized by systemic oxidative stress because of severe obesity, hypertriglyceridaemia, hyperglycaemia and hyperinsulinaemia. We investigated lipid peroxidation and vascular endothelial growth factor (VEGF) expression in the skin of KK A y obese mice. We also investigated the effect of lipid peroxidation derivatives on VEGF production and proliferation in human epidermal keratinocyte cell line (HaCaT). The lipid peroxidation level in the mouse skin tissue was determined by measuring the levels of thiobarbituric acid‐reactive substances. The levels of VEGF expression, p44/p42 mitogen‐activated protein kinase (MAPK) activation and CD36 expression were analysed by Western blot. Their localization was examined by immunofluorescence. For the in vitro experiments, an enzyme‐linked immunosorbent assay was utilized to measure VEGF secretion in the medium. In vitro experiments demonstrated that lipid peroxidation derivatives increased VEGF production in HaCaT cells, which was blocked by a p44/p42 MAPK inhibitor and anti‐CD36 antibody. We observed increased levels of lipid peroxidation derivatives, p44/p42 MAPK activation and VEGF expression in the skin of KK A y obese mice. Notably, pitavastatin, an inhibitor of competitive 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase, suppressed all of these processes. Our results suggest that lipid peroxidation induces VEGF expression via CD36 and p44/p42 MAPK pathway in the skin of obese mice.