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Endoplasmic Reticulum Membrane Contact Sites, Lipid Transport, and Neurodegeneration
被引:17
|作者:
Guillen-Samander, Andres
[1
,2
,3
]
De Camilli, Pietro
[1
,2
,3
]
机构:
[1] Yale Univ, Howard Hughes Med Inst, Program Cellular Neurosci Neurodegenerat & Repair, Dept Neurosci,Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Howard Hughes Med Inst, Program Cellular Neurosci Neurodegenerat & Repair, Sch Med,Dept Cell Biol, New Haven, CT 06520 USA
[3] Aligning Sci Parkinsons ASAP, Collaborat Res Network, Chevy Chase, MD 20815 USA
来源:
基金:
美国国家卫生研究院;
关键词:
KINASE-ASSOCIATED NEURODEGENERATION;
DE-NOVO MUTATIONS;
PARKINSONS-DISEASE;
PROTEIN VAP;
FFAT MOTIF;
MITOCHONDRIAL DYSFUNCTION;
BINDING PROTEIN;
ER CONTACT;
GENE;
FORM;
D O I:
10.1101/cshperspect.a041257
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The Endoplasmic Reticulum (ER) is an endomembrane system that plays a multiplicity of roles in cell physiology and populates even the most distal cell compartments, including dendritic tips and axon terminals of neurons. Some of its functions are achieved by a cross talk with other intracellular membranous organelles and with the plasma membrane at membrane contacts sites (MCSs). As the ER synthesizes most membrane lipids, lipid exchanges mediated by lipid transfer proteins at MCSs are a particularly important aspect of this cross talk, which synergizes with the cross talk mediated by vesicular transport. Several mutations of genes that encode proteins localized at ER MCSs result in familial neurodegenerative diseases, emphasizing the importance of the normal lipid traffic within cells for a healthy brain. Here, we provide an overview of such diseases, with a specific focus on proteins that directly or indirectly impact lipid transport.
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页数:19
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