Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients

<p>Abstract</p> <p>The PARK7 gene encodes a protein, DJ-1, with several functions such as protection of cells from oxidative stress, sperm maturation and fertilization, and chaperone activity. Mutations in the PARK7 gene are associated with autosomal recessive early-onset Parkinson...

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Main Authors: Sue Lucia, Beach Thomas, He Ping, Nural Hikmet, Xia Weiming, Shen Yong
Format: Article
Language:English
Published: BMC 2009-06-01
Series:Molecular Neurodegeneration
Online Access:http://www.molecularneurodegeneration.com/content/4/1/23
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spelling doaj-f20f17a16db14e2bb6725b4c562114ab2020-11-25T00:19:55ZengBMCMolecular Neurodegeneration1750-13262009-06-01412310.1186/1750-1326-4-23Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patientsSue LuciaBeach ThomasHe PingNural HikmetXia WeimingShen Yong<p>Abstract</p> <p>The PARK7 gene encodes a protein, DJ-1, with several functions such as protection of cells from oxidative stress, sperm maturation and fertilization, and chaperone activity. Mutations in the PARK7 gene are associated with autosomal recessive early-onset Parkinson's disease (PD). DJ-1 has been reported to be expressed in multiple cells in the central nerve system. Here, by using both native and denatured Western blots, we examined levels of total DJ-1 and high molecular weight complexes of DJ-1 (HMW) in both the substantia nigra and cortex from rapidly autopsied 18 PD and 9 non-pathological control (NPC) brains. We have discovered that the level of total DJ-1 protein is significantly reduced in the substantia nigra in brains of sporadic PD patients. Moreover, in the PD cortex mitochondria fraction, the HMW DJ-1 complex is significantly lower than in the NPC. These results suggest abnormal DJ-1 expression levels and DJ-1 complex changes may contribute to PD pathogenesis.</p> http://www.molecularneurodegeneration.com/content/4/1/23
collection DOAJ
language English
format Article
sources DOAJ
author Sue Lucia
Beach Thomas
He Ping
Nural Hikmet
Xia Weiming
Shen Yong
spellingShingle Sue Lucia
Beach Thomas
He Ping
Nural Hikmet
Xia Weiming
Shen Yong
Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
Molecular Neurodegeneration
author_facet Sue Lucia
Beach Thomas
He Ping
Nural Hikmet
Xia Weiming
Shen Yong
author_sort Sue Lucia
title Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
title_short Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
title_full Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
title_fullStr Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
title_full_unstemmed Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients
title_sort dissembled dj-1 high molecular weight complex in cortex mitochondria from parkinson's disease patients
publisher BMC
series Molecular Neurodegeneration
issn 1750-1326
publishDate 2009-06-01
description <p>Abstract</p> <p>The PARK7 gene encodes a protein, DJ-1, with several functions such as protection of cells from oxidative stress, sperm maturation and fertilization, and chaperone activity. Mutations in the PARK7 gene are associated with autosomal recessive early-onset Parkinson's disease (PD). DJ-1 has been reported to be expressed in multiple cells in the central nerve system. Here, by using both native and denatured Western blots, we examined levels of total DJ-1 and high molecular weight complexes of DJ-1 (HMW) in both the substantia nigra and cortex from rapidly autopsied 18 PD and 9 non-pathological control (NPC) brains. We have discovered that the level of total DJ-1 protein is significantly reduced in the substantia nigra in brains of sporadic PD patients. Moreover, in the PD cortex mitochondria fraction, the HMW DJ-1 complex is significantly lower than in the NPC. These results suggest abnormal DJ-1 expression levels and DJ-1 complex changes may contribute to PD pathogenesis.</p>
url http://www.molecularneurodegeneration.com/content/4/1/23
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AT nuralhikmet dissembleddj1highmolecularweightcomplexincortexmitochondriafromparkinsonsdiseasepatients
AT xiaweiming dissembleddj1highmolecularweightcomplexincortexmitochondriafromparkinsonsdiseasepatients
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