Autophagy and misfolded proteins in neurodegeneration.
Autophagy and misfolded proteins in neurodegeneration.
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DOI:
10.1016/j.expneurol.2010.11.003
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发表时间:
2012-11
影响因子:
5.3
通讯作者:
Rubinsztein, David C.
中科院分区:
文献类型:
--
作者:
Metcalf, Daniel J.;Garcia-Arencibia, Moises;Hochfeld, Warren E.;Rubinsztein, David C.
The accumulation of misfolded proteins in insoluble aggregates within the neuronal cytoplasm is one of the common pathological hallmarks of most adult-onset human neurodegenerative diseases. The clearance of these misfolded proteins may represent a promising therapeutic strategy in these diseases. The two main routes for intracellular protein degradation are the ubiquitin–proteasome and the autophagy–lysosome pathways. In this review, we will focus on the autophagic pathway, by providing some examples of how impairment at different steps in this degradation pathway is related to different neurodegenerative diseases. We will also consider that upregulating autophagy may be useful in the treatment of some of these diseases. Finally, we discuss how antioxidants, which have been considered to be beneficial in neurodegenerative diseases, can block autophagy, thus potentially compromising their therapeutic potential. ►Autophagy compromise occurs in different neurodegenerative diseases. ►Upregulating autophagy may be useful in the treatment of some neurodegenerative diseases. ►Many different reactive oxygen species scavengers impair autophagy
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影响因子:
3.5
作者:
Aguado C;Sarkar S;Korolchuk VI;Criado O;Vernia S;Boya P;Sanz P;de Córdoba SR;Knecht E;Rubinsztein DC
通讯作者:
Rubinsztein DC
影响因子:
12.4
作者:
Criollo, A.;Maiuri, M. C.;Kroemer, G.
通讯作者:
Kroemer, G.
影响因子:
4
作者:
Jäger, S;Bucci, C;Eskelinen, EL
通讯作者:
Eskelinen, EL
影响因子:
3.3
作者:
Jung, Chang Hwa;Jun, Chang Bong;Kim, Do-Hyung
通讯作者:
Kim, Do-Hyung
影响因子:
1.5
作者:
Kimura, Shunsuke;Noda, Takeshi;Yoshimori, Tamotsu
通讯作者:
Yoshimori, Tamotsu