Identification of a new functional splice variant of the enzyme methionine sulphoxide reductase A (MSRA) expressed in rat vascular smooth muscle cells

Abstract

Reactive oxygen species contribute to ageing of the vascular system and development of cardiovascular disease. Methionine-S-sulphoxide, an oxidized form of methionine, is repaired by the enzyme methionine sulphoxide reductase A (MSRA). The enzyme, targeted to mitochondria or the cytosol by alternative splicing, is vital for oxidative stress resistance. This study was designed to examine the endogenous expression and intracellular localization of MSRA in cultured rat aortic vascular smooth muscle cells (VSMCs). We detected robust MSRA immunoreactivity exclusively in mitochondria. Sequence analysis of msrA transcripts revealed the presence of a novel mitochondrial splice variant, msrA2a, in rat VSMCs as well as in aortic tissue preparations. The enzymatic activity of a recombinant MSRA2a protein was confirmed by the reduction of methionine sulphoxide in a model substrate peptide. We conclude that multiple MSRA variants participate in the repair of oxidized proteins in VSMC mitochondria, but that other protective mechanisms may exist in the cytoplasmic compartment.

• Oxidative stress
• vasculature
• MSRA
• protein oxidation
• alternative splicing

Acronyms
methionine sulphoxide	=	met-O
methionine sulphoxide reductase A and B	=	MSRA/B
reactive oxygen species	=	ROS
vascular smooth muscle cell	=	VSMC

Acronyms
methionine sulphoxide	=	met-O
methionine sulphoxide reductase A and B	=	MSRA/B
reactive oxygen species	=	ROS
vascular smooth muscle cell	=	VSMC