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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Series: | Molecular Neurodegeneration |
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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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