Docherty 2018 Atherosclerosis

From Bioblast
Publications in the MiPMap
Docherty CK, Carswell A, Friel E, Mercer JR (2018) Impaired mitochondrial respiration in human carotid plaque atherosclerosis: A potential role for Pink1 in vascular smooth muscle cell energetics. Atherosclerosis 268:1-11.

Β» PMID: 29156421 Open Access

Docherty CK, Carswell A, Friel E, Mercer JR (2018) Atherosclerosis

Abstract: DNA damage and mitochondrial dysfunction are thought to play an essential role in ageing and the energetic decline of vascular smooth muscle cells (VSMCs) essential for maintaining plaque integrity. We aimed to better understand VSMCs and identify potentially useful compensatory pathways that could extend their lifespan. Moreover, we wanted to assess if defects in mitochondrial respiration exist in human atherosclerotic plaques and to identify the appropriate markers that may reflect a switch in VSMC energy metabolism.

Human plaque tissue and cells were assessed for composition and evidence of DNA damage, repair capacity and mitochondrial dysfunction. Fresh plaque tissue was evaluated using high resolution oxygen respirometry to assess oxidative metabolism. Recruitment and processing of the mitochondrial regulator of autophagy Pink1 kinase was investigated in combination with transcriptional and protein markers associated with a potential switch to a more glycolytic metabolism.

Human VSMC have increased nuclear (nDNA) and mitochondrial (mtDNA) damage and reduced repair capacity. A subset of VSMCs within plaque cap had decreased oxidative phosphorylation and expression of Pink1 kinase. Plaque cells demonstrated increased glycolytic activity in response to loss of mitochondrial function. A potential compensatory glycolytic program may act as energetic switch via AMP kinase (AMPK) and hexokinase 2 (Hex2).

We have identified a subset of plaque VSMCs required for plaque stability that have increased mitochondrial dysfunction and decreased oxidative phosphorylation. Pink1 kinase may initiate a cellular response to promote a compensatory glycolytic program associated with upregulation of AMPK and Hex2.

Copyright Β© 2017 The Authors. Published by Elsevier B.V. All rights reserved. β€’ Keywords: AMPK, Atherosclerosis, Glycolysis, Metabolism, Mitochondria, Oxidative phosphorylation, Pink-1, Vascular smooth muscle cells β€’ Bioblast editor: Kandolf G β€’ O2k-Network Lab: UK Glasgow Mercer J

Labels: MiParea: Respiration, mtDNA;mt-genetics, nDNA;cell genetics  Pathology: Aging;senescence, Cardiovascular 

Organism: Human  Tissue;cell: Endothelial;epithelial;mesothelial cell  Preparation: Permeabilized tissue 

Coupling state: OXPHOS  Pathway: N, CIV, NS, ROX  HRR: Oxygraph-2k 

Labels, 2018-01 

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