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α-突触核蛋白与自噬作为神经退行性变的共同步骤。

Alpha-synuclein and autophagy as common steps in neurodegeneration.

作者信息

Ferrucci Michela, Pasquali Livia, Ruggieri Stefano, Paparelli Antonio, Fornai Francesco

机构信息

Department of Human Morphology and Applied Biology, University of Pisa, Via Roma 55, Pisa, Italy.

出版信息

Parkinsonism Relat Disord. 2008;14 Suppl 2:S180-4. doi: 10.1016/j.parkreldis.2008.04.025. Epub 2008 Jun 25.

Abstract

The major component of Lewy bodies in Parkinson's disease (PD) is alpha-synuclein, which is considered as a substrate of the ubiquitin-proteasome (UP) system, although autophagy seems to be equally involved. Here we discuss the co-existence of alpha-synuclein and proteins belonging to the UP system within autophagic granules, further developing as neuronal inclusions. We hypothesize that, following slight insults, both UP and autophagy are induced; if toxic stimuli are prolonged, these pathways are overwhelmed and cell death occurs. We then indicate a protective role of autophagy in PD and suggest it as a therapeutic target to slow down the progression of the disease.

摘要

帕金森病(PD)中路易小体的主要成分是α-突触核蛋白,尽管自噬似乎也同样参与其中,但它被认为是泛素-蛋白酶体(UP)系统的底物。在此我们讨论α-突触核蛋白与UP系统中的蛋白质在自噬颗粒中共存的情况,这些自噬颗粒会进一步发展为神经元内含物。我们假设,在受到轻微损伤后,UP和自噬都会被诱导;如果毒性刺激持续存在,这些途径就会不堪重负,导致细胞死亡。然后我们指出自噬在帕金森病中的保护作用,并建议将其作为减缓疾病进展的治疗靶点。

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