Peroxisomes in cardiomyocytes and the peroxisome / peroxisome proliferator-activated receptor-loop

过氧化物酶体 过氧化物酶体增殖物 过氧化物酶体增殖物激活受体γ 过氧化物酶体增殖物激活受体α 过氧化物酶体增殖物激活受体 细胞生物学 生物 化学 受体 生物化学 核受体 基因 转录因子
作者
Claudia Colasante,Jiangping Chen,Barbara Ahlemeyer,Eveline Baumgart‐Vogt
出处
期刊:Thrombosis and Haemostasis [Thieme Medical Publishers (Germany)]
卷期号:113 (03): 452-463 被引量:47
标识
DOI:10.1160/th14-06-0497
摘要

Summary It is well established that the heart is strongly dependent on fatty acid metabolism. In cardiomyocytes there are two distinct sites for the β-oxidisation of fatty acids: the mitochondrion and the peroxisome. Although the metabolism of these two organelles is believed to be tightly coupled, the nature of this relationship has not been fully investigated. Recent research has established the significant contribution of mitochondrial function to cardiac ATP production under normal and pathological conditions. In contrast, limited information is available on peroxisomal function in the heart. This is despite these organelles harbouring metabolic pathways that are potentially cardioprotective, and findings that patients with peroxisomal diseases, such as adult Refsum’s disease, can develop heart failure. In this article, we provide a comprehensive overview on the current knowledge of peroxisomes and the regulation of lipid metabolism by PPARs in cardiomyocytes. We also present new experimental evidence on the differential expression of peroxisome-related genes in the heart chambers and demonstrate that even a mild peroxisomal biogenesis defect (Pex11α-/- ) can induce profound alterations in the cardiomyocyte’s peroxisomal compartment and related gene expression, including the concomitant deregulation of specific PPARs. The possible impact of peroxisomal dysfunction in the heart is discussed and a model for the modulation of myocardial metabolism via a peroxisome/PPAR-loop is proposed.

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