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过氧化物酶体的分裂与增殖

Fission and proliferation of peroxisomes.

作者信息

Schrader M, Bonekamp N A, Islinger M

机构信息

Department of Biology, University of Aveiro, Aveiro, Portugal.

出版信息

Biochim Biophys Acta. 2012 Sep;1822(9):1343-57. doi: 10.1016/j.bbadis.2011.12.014. Epub 2011 Dec 31.

DOI:10.1016/j.bbadis.2011.12.014
PMID:22240198
Abstract

Peroxisomes are remarkably dynamic, multifunctional organelles, which react to physiological changes in their cellular environment and adopt their morphology, number, enzyme content and metabolic functions accordingly. At the organelle level, the key molecular machinery controlling peroxisomal membrane elongation and remodeling as well as membrane fission is becoming increasingly established and defined. Key players in peroxisome division are conserved in animals, plants and fungi, and key fission components are shared with mitochondria. However, the physiological stimuli and corresponding signal transduction pathways regulating and modulating peroxisome maintenance and proliferation are, despite a few exceptions, largely unexplored. There is emerging evidence that peroxisomal dynamics and proper regulation of peroxisome number and morphology are crucial for the physiology of the cell, as well as for the pathology of the organism. Here, we discuss several key aspects of peroxisomal fission and proliferation and highlight their association with certain diseases. We address signaling and transcriptional events resulting in peroxisome proliferation, and focus on novel findings concerning the key division components and their interplay. Finally, we present an updated model of peroxisomal growth and division. This article is part of a Special Issue entitled: Metabolic Functions and Biogenesis of Peroxisomes in Health and Disease.

摘要

过氧化物酶体是非常动态的多功能细胞器,它们会对细胞环境中的生理变化做出反应,并相应地改变其形态、数量、酶含量和代谢功能。在细胞器层面,控制过氧化物酶体膜伸长、重塑以及膜分裂的关键分子机制正日益明确。过氧化物酶体分裂的关键参与者在动物、植物和真菌中是保守的,并且关键的分裂成分与线粒体共享。然而,尽管有一些例外情况,但调节和调控过氧化物酶体维持和增殖的生理刺激及相应信号转导途径在很大程度上仍未被探索。越来越多的证据表明,过氧化物酶体动力学以及过氧化物酶体数量和形态的适当调节对于细胞生理以及生物体病理都至关重要。在此,我们讨论过氧化物酶体分裂和增殖的几个关键方面,并强调它们与某些疾病的关联。我们阐述导致过氧化物酶体增殖的信号传导和转录事件,并聚焦于有关关键分裂成分及其相互作用的新发现。最后,我们提出一个更新的过氧化物酶体生长和分裂模型。本文是名为“健康与疾病中过氧化物酶体的代谢功能与生物发生”特刊的一部分。

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