Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases

被引:546
作者
Hetz, Claudio [1 ,2 ,3 ,4 ]
Mollereau, Bertrand [5 ]
机构
[1] Univ Chile, Fac Med, Biomed Neurosci Inst, Santiago 7, Chile
[2] Univ Chile, Inst Biomed Sci, Ctr Mol Studies Cell, Program Cellular & Mol Biol, Santiago, Chile
[3] Neurounion Biomed Fdn, Santiago, Chile
[4] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[5] Univ Lyon, CNRS, UMR5239,Lab Mol Biol Cell, Ecole Normale Super Lyon,Biosci Lyon Gerland UMS3, F-69364 Lyon, France
关键词
UNFOLDED-PROTEIN RESPONSE; AMYOTROPHIC-LATERAL-SCLEROSIS; SPINAL-CORD-INJURY; SODIUM 4-PHENYLBUTYRATE PROTECTS; IMPROVES FUNCTIONAL RECOVERY; LYSOSOMAL STORAGE DISORDERS; TRANSCRIPTION FACTOR XBP-1; AMYLOID PRECURSOR PROTEIN; GAMMA-SECRETASE ACTIVITY; SYNUCLEINOPATHY IN-VIVO;
D O I
10.1038/nrn3689
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The unfolded protein response (UPR) is a homeostatic mechanism by which cells regulate levels of misfolded proteins in the endoplasmic reticulum (ER). Although it is well characterized in non-neuronal cells, a proliferation of papers over the past few years has revealed a key role for the UPR in normal neuronal function and as an important driver of neurodegenerative diseases. A complex scenario is emerging in which distinct UPR signalling modules have specific and even opposite effects on neurodegeneration depending on the disease context. Here, we provide an overview of the most recent findings addressing the biological relevance of ER stress in the nervous system.
引用
收藏
页码:233 / 249
页数:17
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