Evidence map›Paper›PMID 20924620›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2011

Nuclear translocation of anamorsin during drug-induced dopaminergic neurodegeneration in culture and in rat brain.

Kyung-Ah Park, Nuri Yun, Dong-Ik Shin, So Yoen Choi, Hyun Kim, Won-Ki Kim, Yuzuru Kanakura, Hirohiko Shibayama, Young J Oh

Abstract read
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In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Epigenetic role for the conserved Fe-S cluster biogenesis protein AtDRE2 in Arabidopsis thaliana.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  7. Anamorsin, a novel caspase-3 substrate in neurodegeneration.The Journal of biological chemistry · 2014
    Article
  8. Human anamorsin binds [2Fe-2S] clusters with unique electronic properties.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2013
    Article
  9. Article
  10. Microarray expression profiling in 6-hydroxydopamine-induced dopaminergic neuronal cell death.Journal of neural transmission (Vienna, Austria : 1996) · 2011
    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

9 authors at 4 institutions in 2 countries.

Kyung-Ah ParkDepartment of Biology, Yonsei University College of Life Science and Biotechnology, 134 Shincheon-dong Seodaemoon-gu, Seoul, 120-749, Korea.
Nuri Yun
Dong-Ik Shin
So Yoen Choi
Hyun Kim
Won-Ki Kim
Yuzuru Kanakura
Hirohiko Shibayama
Young J Oh
Yonsei University · KRKorea University · JPOsaka University · JPKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anamorsin, also called cytokine-induced apoptosis inhibitor 1 (CIAPIN1), was recently identified to confer resistance to apoptosis induced by growth factor deprivation and to be indispensible for hematopoiesis. Recently, it was demonstrated that anamorsin is also widely distributed in both fetal and adult tissues. In this study, we evaluated the tissue distribution of anamorsin in the central nervous system (CNS) during development. In situ hybridization and immunoblot analyses revealed that anamorsin mRNA and protein were both highly and widely expressed in various regions of the CNS, including the cerebral cortex, hippocampus, midbrain, cerebellum, medulla, and spinal cord. Based on these findings, we examined its cellular localization during drug-induced neurodegeneration in MN9D dopaminergic cells. Both immunocytochemical localization and immunoblot analyses indicated that cytosolic anamorsin was translocated into the nucleus in a time-dependent manner following treatment with a reactive oxygen species (ROS)-inducing drug, 6-hydroxydopamine (6-OHDA). Treatment of cells with the apoptosis-inducing reagent, staurosporine, did not appear to cause translocation of anamorsin into the nucleus. When cells were treated with the nuclear export inhibitor, Leptomycin B, alone or with 6-OHDA, nuclear anamorsin levels increased, indicating that nuclear influx and efflux of anamorsin are regulated by 6-OHDA treatment. In rat brain injected with 6-OHDA, nuclear translocation of anamorsin was identified in certain tyrosine hydroxylase (TH)-positive neurons as well as TH-negative cells. Furthermore, treatment of MN9D cells with hydrogen peroxide or ROS-inducing trace metals caused nuclear translocation of anamorsin. Taken together, our data indicate that nuclear translocation of anamorsin is a ROS-dependent event and may participate in the regulation of transcription of critical molecules during dopaminergic neurodegeneration.

Indexed as

AnimalsApoptosis Regulatory ProteinsBlotting, WesternCell FractionationCells, CulturedDopamineImmunohistochemistryIn Situ HybridizationIntracellular Signaling Peptides and ProteinsMaleMesencephalonNerve DegenerationNeuronsProtein TransportRatsRats, Sprague-DawleyApoptosis Regulatory Proteinscytokine-induced apoptosis inhibitor 1, ratDopamineIntracellular Signaling Peptides and ProteinsReactive Oxygen SpeciesStaurosporine

Identifiers

PMID20924620
OpenAlexW2156495641

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.