Evidence map›Paper›PMID 24475098›Full record

ArticlePloS one2014

BAG5 protects against mitochondrial oxidative damage through regulating PINK1 degradation.

Xuejing Wang, Jifeng Guo, Erkang Fei, Yingfeng Mu, Shuang He, Xiangqian Che, Jieqiong Tan, Kun Xia, Zhuohua Zhang, Guanghui Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. BAG family proteins contributes to autophagy-mediated multidrug resistance of tumor.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  6. Mitochondria in neurodegeneration.Current opinion in physiology · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Mitochondrial Kinase PINK1 in Diabetic Kidney Disease.International journal of molecular sciences · 2021
    Review
  15. PINK1: Multiple mechanisms of neuroprotection.International review of movement disorders · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Chronic treatment with the complex I inhibitor MPPThe Journal of biological chemistry · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Xuejing WangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Jifeng GuoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China ; State Key Laboratory of Medical Genetics, Changsha, Hunan, People's Republic of China ; Human Key Laboratory of Neurodegenerative Disorders, Central South University, Changsha, Hunan, People's Republic of China ; Neurodegenerative Disorders Research Center, Central South University, Changsha, Hunan, People's Republic of China.
Erkang FeiLaboratory of Molecular Neuropathology, National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, People's Republic of China.
Yingfeng MuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Shuang HeDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Xiangqian CheDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Jieqiong TanState Key Laboratory of Medical Genetics, Changsha, Hunan, People's Republic of China.
Kun XiaState Key Laboratory of Medical Genetics, Changsha, Hunan, People's Republic of China.
Zhuohua ZhangState Key Laboratory of Medical Genetics, Changsha, Hunan, People's Republic of China.
Guanghui WangLaboratory of Molecular Neuropathology, National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, People's Republic of China.
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China ; State Key Laboratory of Medical Genetics, Changsha, Hunan, People's Republic of China ; Human Key Laboratory of Neurodegenerative Disorders, Central South University, Changsha, Hunan, People's Republic of China ; Neurodegenerative Disorders Research Center, Central South University, Changsha, Hunan, People's Republic of China.
Central South University · CNChangsha Medical University · CNUniversity of Science and Technology of China · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in PTEN-induced kinase 1 (PINK1) gene cause PARK6 familial Parkinsonism, and loss of the stability of PINK1 may also contribute to sporadic Parkinson's disease (PD). Degradation of PINK1 occurs predominantly through the ubiquitin proteasome system (UPS), however, to date, few of the proteins have been found to regulate the degradation of PINK1. Using the yeast two-hybrid system and pull-down methods, we identified bcl-2-associated athanogene 5 (BAG5), a BAG family member, directly interacted with PINK1. We showed that BAG5 stabilized PINK1 by decreasing the ubiquitination of PINK1. Interestingly, BAG5 rescued MPP(+)- and rotenone-induced mitochondria dysfunction by up-regulating PINK1 in vitro. In PINK1-null mice and MPTP-treated mice, BAG5 significantly increased in the substantia nigra pars compacta (SNpc) although PINK1 was decreased. Our findings indicated that BAG5, as a key protein to stabilize PINK1, is a promising therapeutic tool for preventing mitochondrial dysfunction following oxidative stress.

Indexed as

Oxidative Stress1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAdaptor Proteins, Signal TransducingAnimalsCell LineHumansMiceMitochondriaNeurotoxinsProtein BindingProtein KinasesProtein StabilityProteolysisPTEN-Induced Putative KinaseRotenoneSubstantia Nigra1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAdaptor Proteins, Signal TransducingBAG5 protein, humanNeurotoxinsProtein KinasesPTEN-Induced Putative KinaseRotenone

Identifiers

PMID24475098
PMCPMC3901670
OpenAlexW2025625712

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.