MFN2型
线粒体融合
线粒体分裂
细胞生物学
线粒体
生物
MFN1型
神经退行性变
DNAJA3公司
线粒体生物发生
生物发生
神经科学
线粒体DNA
遗传学
医学
疾病
病理
基因
作者
Prakash G. Kulkarni,Vaibhavi M. Mohire,Pooja K Bhaisa,Mrudula M Joshi,Chitranshi M Puranik,Pranjal P. Waghmare,Tanushree Banerjee
出处
期刊:Mitochondrion
[Elsevier BV]
日期:2023-02-09
卷期号:69: 116-129
被引量:9
标识
DOI:10.1016/j.mito.2023.02.001
摘要
Mitochondria are highly dynamic organelles known to play role in the regulation of several cellular biological processes. However, their dynamics such as number, shape, and biological functions are regulated by mitochondrial fusion and fission process. The balance between the fusion and fission process is most important for the maintenance of mitochondrial structure as well as cellular functions. The alterations within mitochondrial dynamic processes were found to be associated with the progression of neurodegenerative diseases. In recent years, mitofusin-2 (Mfn2), a GTPase has emerged as a multifunctional protein which not only is found to regulate the mitochondrial fusion-fission process but also known to regulate several cellular functions such as mitochondrial metabolism, cellular biogenesis, signalling, and apoptosis via maintaining the ER-mitochondria contact sites. In this review, we summarize the current knowledge of the structural and functional properties of the Mfn2, its transcriptional regulation and their roles in several cellular functions with a focus on current advances in the pathogenesis of neurodegenerative diseases.
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