Mitochondria-associated membranes as hubs for neurodegeneration

被引:163
作者
Krols, Michiel [1 ,2 ,3 ]
van Isterdael, Gert [4 ,5 ]
Asselbergh, Bob [2 ,3 ]
Kremer, Anna [6 ,7 ]
Lippens, Saskia [6 ,7 ]
Timmerman, Vincent [1 ,2 ,3 ]
Janssens, Sophie [4 ,5 ]
机构
[1] Univ Antwerp VIB, Dept Mol Genet, Peripheral Neuropathy Grp, B-2610 Antwerp, Belgium
[2] Univ Antwerp VIB, Dept Mol Genet, B-2610 Antwerp, Belgium
[3] Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium
[4] Univ Ghent VIB, Inflammat Res Ctr, Unit Immunoregulat & Mucosal Immunol, Zwijnaarde, Belgium
[5] Univ Ghent, Dept Internal Med, B-9000 Ghent, Belgium
[6] VIB, Inflammat Res Ctr, Bio Imaging Core, Ghent, Belgium
[7] VIB, VIB Bio Imaging Core, Ghent, Belgium
关键词
ENDOPLASMIC-RETICULUM MEMBRANES; ER-MITOCHONDRIA; MITOFUSIN; ALZHEIMERS-DISEASE; CA2+; PROTEIN; MUTATIONS; FISSION; COMPLEX; LOCALIZATION;
D O I
10.1007/s00401-015-1528-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There is a growing appreciation that membrane-bound organelles in eukaryotic cells communicate directly with one another through direct membrane contact sites. Mitochondria-associated membranes are specialized subdomains of the endoplasmic reticulum that function as membrane contact sites between the endoplasmic reticulum and mitochondria. These sites have emerged as major players in lipid metabolism and calcium signaling. More recently also autophagy and mitochondrial dynamics have been found to be regulated at ER-mitochondria contact sites. Neurons critically depend on mitochondria-associated membranes as a means to exchange metabolites and signaling molecules between these organelles. This is underscored by the fact that genes affecting mitochondrial and endoplasmic reticulum homeostasis are clearly overrepresented in several hereditary neurodegenerative disorders. Conversely, the processes affected by the contact sites between the endoplasmic reticulum and mitochondria are widely implicated in neurodegeneration. This review will focus on the most recent data addressing the structural composition and function of the mitochondria-associated membranes. In addition, the 3D morphology of the contact sites as observed using volume electron microscopy is discussed. Finally, it will highlight the role of several key proteins associated with these contact sites that are involved not only in dementias, amyotrophic lateral sclerosis and Parkinson's disease, but also in axonopathies such as hereditary spastic paraplegia and Charcot-Marie-Tooth disease.
引用
收藏
页码:505 / 523
页数:19
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