The Peroxisome-Mitochondria Connection: How and Why?

被引:240
作者
Fransen, Marc [1 ]
Lismont, Celien [1 ]
Walton, Paul [2 ]
机构
[1] Univ Leuven, KU Leuven, Dept Cellular & Mol Med, Lab Lipid Biochem & Prot Interact, B-3000 Leuven, Belgium
[2] Univ Western Ontario, Dept Anat & Cell Biol, London, ON N6A 3K7, Canada
关键词
peroxisomes; mitochondria; fatty acid oxidation; reactive oxygen species; interorganelle crosstalk; organelle abundance; organelle dysfunction; human disease; ACID BETA-OXIDATION; DYNAMIN-LIKE PROTEIN-1; CHAIN FATTY-ACID; ACYL-COA OXIDASE; MAMMALIAN PEROXISOMES; HYDROGEN-PEROXIDE; ENDOPLASMIC-RETICULUM; ZELLWEGER-SYNDROME; RAT-LIVER; PHYSIOLOGICAL ROLES;
D O I
10.3390/ijms18061126
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the past decades, peroxisomes have emerged as key regulators in overall cellular lipid and reactive oxygen species metabolism. In mammals, these organelles have also been recognized as important hubs in redox-, lipid-, inflammatory-, and innate immune-signaling networks. To exert these activities, peroxisomes must interact both functionally and physically with other cell organelles. This review provides a comprehensive look of what is currently known about the interconnectivity between peroxisomes and mitochondria within mammalian cells. We first outline how peroxisomal and mitochondrial abundance are controlled by common sets of cis- and trans-acting factors. Next, we discuss how peroxisomes and mitochondria may communicate with each other at the molecular level. In addition, we reflect on how these organelles cooperate in various metabolic and signaling pathways. Finally, we address why peroxisomes and mitochondria have to maintain a healthy relationship and why defects in one organelle may cause dysfunction in the other. Gaining a better insight into these issues is pivotal to understanding how these organelles function in their environment, both in health and disease.
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页数:24
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