La maladie de Parkinson en France (serveur d'exploration)

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SLC35D3 increases autophagic activity in midbrain dopaminergic neurons by enhancing BECN1-ATG14-PIK3C3 complex formation

Identifieur interne : 000099 ( Main/Exploration ); précédent : 000098; suivant : 000100

SLC35D3 increases autophagic activity in midbrain dopaminergic neurons by enhancing BECN1-ATG14-PIK3C3 complex formation

Auteurs : Z. B. Wei ; Y. F. Yuan ; F. Jaouen [France] ; M. S. Ma ; C. J. Hao ; Z. Zhang ; Q. Chen ; Z. Yuan ; C. Beurrier [France] ; W. Li

Source :

RBID : Hal:hal-01445052

English descriptors

Abstract

Searching for new regulators of autophagy involved in selective dopaminergic (DA) neuron loss is a hallmark in the pathogenesis of Parkinson disease (PD). We here report that an endoplasmic reticulum (ER)-associated transmembrane protein SLC35D3 is selectively expressed in subsets of midbrain DA neurons in about 10% TH (tyrosine hydroxylase)-positive neurons in the substantia nigra pars compacta (SNc) and in about 22% TH-positive neurons in the ventral tegmental area (VTA). Loss of SLC35D3 in ros (roswell mutant) mice showed a reduction of 11.9% DA neurons in the SNc and 15.5% DA neuron loss in the VTA with impaired autophagy. We determined that SLC35D3 enhanced the formation of the BECN1-ATG14-PIK3C3 complex to induce autophagy. These results suggest that SLC35D3 is a new regulator of tissue-specific autophagy and plays an important role in the increased autophagic activity required for the survival of subsets of DA neurons.

Url:
DOI: 10.1080/15548627.2016.1179402. Epub 2016 May 12.


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Searching for new regulators of autophagy involved in selective dopaminergic (DA) neuron loss is a hallmark in the pathogenesis of Parkinson disease (PD). We here report that an endoplasmic reticulum (ER)-associated transmembrane protein SLC35D3 is selectively expressed in subsets of midbrain DA neurons in about 10% TH (tyrosine hydroxylase)-positive neurons in the substantia nigra pars compacta (SNc) and in about 22% TH-positive neurons in the ventral tegmental area (VTA). Loss of SLC35D3 in ros (roswell mutant) mice showed a reduction of 11.9% DA neurons in the SNc and 15.5% DA neuron loss in the VTA with impaired autophagy. We determined that SLC35D3 enhanced the formation of the BECN1-ATG14-PIK3C3 complex to induce autophagy. These results suggest that SLC35D3 is a new regulator of tissue-specific autophagy and plays an important role in the increased autophagic activity required for the survival of subsets of DA neurons. </div>
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<name sortKey="Zhang, Z" sort="Zhang, Z" uniqKey="Zhang Z" first="Z." last="Zhang">Z. Zhang</name>
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<name sortKey="Jaouen, F" sort="Jaouen, F" uniqKey="Jaouen F" first="F." last="Jaouen">F. Jaouen</name>
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<name sortKey="Beurrier, C" sort="Beurrier, C" uniqKey="Beurrier C" first="C." last="Beurrier">C. Beurrier</name>
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