Role of Cardiolipin in Mitochondrial Function and Dynamics in Health and Disease: Molecular and Pharmacological Aspects

被引:311
作者
Paradies, Giuseppe [1 ]
Paradies, Valeria [2 ]
Ruggiero, Francesca M. [1 ]
Petrosillo, Giuseppe [3 ]
机构
[1] Univ Bari, Dept Biosci Biotechnol & Biopharmaceut, I-70125 Bari, Italy
[2] Maasstad Ziekenhuis, NL-3079 DZ Rotterdam, Netherlands
[3] Natl Res Council CNR, Inst Biomembranes Bioenerget & Mol Biotechnol IBI, I-70126 Bari, Italy
关键词
Cardiolipin; mitochondrial structure-function; physiopathology; pharmacological agents; ELECTRON-TRANSPORT CHAIN; PERMEABILITY TRANSITION PORE; CYTOCHROME-C; BARTH-SYNDROME; OXIDATIVE-STRESS; ATP SYNTHASE; COMPLEX-I; SUPRAMOLECULAR ORGANIZATION; CONTACT SITE; DYSFUNCTION;
D O I
10.3390/cells8070728
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In eukaryotic cells, mitochondria are involved in a large array of metabolic and bioenergetic processes that are vital for cell survival. Phospholipids are the main building blocks of mitochondrial membranes. Cardiolipin (CL) is a unique phospholipid which is localized and synthesized in the inner mitochondrial membrane (IMM). It is now widely accepted that CL plays a central role in many reactions and processes involved in mitochondrial function and dynamics. Cardiolipin interacts with and is required for optimal activity of several IMM proteins, including the enzyme complexes of the electron transport chain (ETC) and ATP production and for their organization into supercomplexes. Moreover, CL plays an important role in mitochondrial membrane morphology, stability and dynamics, in mitochondrial biogenesis and protein import, in mitophagy, and in different mitochondrial steps of the apoptotic process. It is conceivable that abnormalities in CL content, composition and level of oxidation may negatively impact mitochondrial function and dynamics, with important implications in a variety of pathophysiological situations and diseases. In this review, we focus on the role played by CL in mitochondrial function and dynamics in health and diseases and on the potential of pharmacological modulation of CL through several agents in attenuating mitochondrial dysfunction.
引用
收藏
页数:21
相关论文
共 145 条
[1]   Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography [J].
Acehan, Devrim ;
Xu, Yang ;
Stokes, David L. ;
Schlame, Michael .
LABORATORY INVESTIGATION, 2007, 87 (01) :40-48
[2]   Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria [J].
Acehan, Devrim ;
Malhotra, Ashim ;
Xu, Yang ;
Ren, Mindong ;
Stokes, David L. ;
Schlame, Michael .
BIOPHYSICAL JOURNAL, 2011, 100 (09) :2184-2192
[3]   BARTH SYNDROME - CLINICAL-FEATURES AND CONFIRMATION OF GENE LOCALIZATION TO DISTAL XQ28 [J].
ADES, LC ;
GEDEON, AK ;
WILSON, MJ ;
LATHAM, M ;
PARTINGTON, MW ;
MULLEY, JC ;
NELSON, J ;
LUI, K ;
SILLENCE, DO .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (03) :327-334
[4]   Supramolecular Organization of Respiratory Complexes [J].
Antonio Enriquez, Jose .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 78, 2016, 78 :533-561
[5]   The role of nonbilayer phospholipids in mitochondrial structure and function [J].
Ball, Writoban Basu ;
Neff, John K. ;
Gohil, Vishal M. .
FEBS LETTERS, 2018, 592 (08) :1273-1290
[6]   Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin [J].
Ban, Tadato ;
Ishihara, Takaya ;
Kohno, Hiroto ;
Saita, Shotaro ;
Ichimura, Ayaka ;
Maenaka, Katsumi ;
Oka, Toshihiko ;
Mihara, Katsuyoshi ;
Ishihara, Naotada .
NATURE CELL BIOLOGY, 2017, 19 (07) :856-+
[7]   Peroxidase Mechanism of Lipid-dependent Cross-linking of Synuclein with Cytochrome c PROTECTION AGAINST APOPTOSIS VERSUS DELAYED OXIDATIVE STRESS IN PARKINSON DISEASE [J].
Bayir, Huelya ;
Kapralov, Alexandr A. ;
Jiang, Janfei ;
Huang, Zhentai ;
Tyurina, Yulia Y. ;
Tyurin, Vladimir A. ;
Zhao, Qing ;
Belikova, Natalia A. ;
Vlasova, Irina I. ;
Maeda, Akihiro ;
Zhu, Jianhui ;
Na, Hye-Mee ;
Mastroberardino, Pier-Giorgio ;
Sparvero, Louis J. ;
Amoscato, Andrew A. ;
Chu, Charleen T. ;
Greenamyre, John T. ;
Kagan, Valerian E. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (23) :15951-15969
[8]   Peroxidase activity and structural transitions of cytochrome c bound to cardiolipin-containing membranes [J].
Belikova, NA ;
Vladimirov, YA ;
Osipov, AN ;
Kapralov, AA ;
Tyurin, VA ;
Potapovich, MV ;
Basova, LV ;
Peterson, J ;
Kurnikov, IV ;
Kagan, VE .
BIOCHEMISTRY, 2006, 45 (15) :4998-5009
[9]   The mitochondrial permeability transition pore: Molecular nature and role as a target in cardioprotection [J].
Bernardi, Paolo ;
Di Lisa, Fabio .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2015, 78 :100-106
[10]   The mitochondrial permeability transition pore in AD 2016: An update [J].
Biasutto, Lucia ;
Azzolini, Michele ;
Szabo, Ildiko ;
Zoratti, Mario .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (10) :2515-2530