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DOI 10.1016/j.biocel.2016.06.013

Медицинская библиотека · The international journal of biochemistry & cell biology · 2016

Pigment epithelium-derived factor stimulates skeletal muscle glycolytic activity through NADPH oxidase-dependent reactive oxygen species production.

Carnagarin Revathy, Carlessi Rodrigo, Newsholme Philip, Dharmarajan Arun M, Dass Crispin R

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Pigment epithelium-derived factor is a multifunctional serpin implicated in insulin resistance in metabolic disorders. Recent evidence suggests that exposure of peripheral tissues such as skeletal muscle to PEDF has profound metabolic consequences with predisposition towards chronic conditions such as obesity, type 2 diabetes, metabolic syndrome and polycystic ovarian syndrome. Chronic inflammation shifts muscle metabolism towards increased glycolysis and decreased oxidative metabolism. In the present study, we demonstrate a novel effect of PEDF on cellular metabolism in mouse cell line (C2C12) and human primary skeletal muscle cells. PEDF addition to skeletal muscle cells induced enhanced phospholipase A2 activity. This was accompanied with increased production of reactive oxygen species in a nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-dependent manner that triggered a shift towards a more glycolytic phenotype. Extracellular flux analysis and glucose consumption assays demonstrated that PEDF treatment resulted in enhanced glycolysis but did not change mitochondrial respiration. Our results demonstrate that skeletal muscle cells express a PEDF-inducible oxidant generating system that enhances glycolysis but is sensitive to antioxidants and NADPH oxidase inhibition.

Для цитирования: Carnagarin Revathy, Carlessi Rodrigo, Newsholme Philip, Dharmarajan Arun M, Dass Crispin R. Pigment epithelium-derived factor stimulates skeletal muscle glycolytic activity through NADPH oxidase-dependent reactive oxygen species production.. The international journal of biochemistry & cell biology. 2016. DOI: 10.1016/j.biocel.2016.06.013.

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