Evidence map›Paper›PMID 21632930›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Phosphoinositide 3-kinase enhancer regulates neuronal dendritogenesis and survival in neocortex.

Chi Bun Chan, Xia Liu, Sompol Pradoldej, Chunhai Hao, Jie An, Manuel Yepes, Hongbo R Luo, Keqiang Ye

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
  2. Genome research · 2024
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Defective phosphoinositide metabolism in autism.Journal of neuroscience research · 2017
    Review
  13. Neurogenesis in Stroke Recovery.Translational stroke research · 2017
    Review
  14. α-Synuclein binds and sequesters PIKE-L into Lewy bodies, triggering dopaminergic cell death via AMPK hyperactivation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Norepinephrine Protects against Amyloid-β Toxicity via TrkB.Journal of Alzheimer's disease : JAD · 2015
    Article
  20. 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

8 authors.

Chi Bun ChanDepartment of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Xia Liu
Sompol Pradoldej
Chunhai Hao
Jie An
Manuel Yepes
Hongbo R Luo
Keqiang Ye

Funding

Nuclear GTPase PIKE Regulation and FunctionsR01NS045627 · NINDS · EMORY UNIVERSITY · PI YE, KEQIANG · 2004 to 2013
$3.1M
Protease-Regulated Blood Brain Barrier PermeabilityR01NS049478 · NINDS · EMORY UNIVERSITY · PI YEPES, MANUEL SALVADOR · 2005 to 2008
$1.2M
NINDS NIH HHS R01 NS045627NINDS NIH HHS R01 NS049478NINDS NIH HHS R01 NS45627NINDS NIH HHS R01 NS49478
6 · The paper itself

Abstract

Phosphoinositide 3-kinase enhancer (PIKE) binds and enhances phosphatidylinositol 3-kinase (PI3K)/Akt activities. However, its physiological functions in brain have never been explored. Here we show that PIKE is important in regulating the neuronal survival and development of neocortex. During development, enhanced apoptosis is observed in the ventricular zone of PIKE knock-out (PIKE(-/-)) cortex. Moreover, PIKE(-/-) neurons show reduced dendritic complexity, dendritic branch length, and soma size. These defects are due to the reduced PI3K/Akt activities in PIKE(-/-) neurons, as the impaired dendritic arborization can be rescued when PI3K/Akt cascade is augmented in vitro or in PIKE(-/-)PTEN(-/-) double-knock-out mice. Interestingly, PIKE(-/-) mice display behavioral abnormality in locomotion and spatial navigation. Because of the diminished PI3K/Akt activities, PIKE(-/-) neurons are more vulnerable to glutamate- or stroke-induced neuronal cell death. Together, our data established the critical role of PIKE in regulating neuronal survival and development by substantiating the PI3K/Akt pathway.

Indexed as

AnimalsApoptosisBrain-Derived Neurotrophic FactorCell Culture TechniquesCell SurvivalDendritesGlutamic AcidGTP PhosphohydrolasesInfarction, Middle Cerebral ArteryLocomotionMiceMice, Inbred C57BLMice, KnockoutNeocortexNerve Tissue ProteinsNeurogenesisBrain-Derived Neurotrophic FactorGlutamic AcidGTP PhosphohydrolasesNerve Tissue ProteinsPIKE protein, mouseProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, mouse

Identifiers

PMID21632930
PMCPMC3551346

What OpenQuestion holds

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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.