Evidence map›Paper›PMID 24209749›Full record

ArticleCell reports2013

Protein phosphatase 4 and Smek complex negatively regulate Par3 and promote neuronal differentiation of neural stem/progenitor cells.

Jungmook Lyu, Hee-Ryang Kim, Vicky Yamamoto, Si Ho Choi, Zong Wei, Choun-Ki Joo, Wange Lu

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  12. The Roles of Par3, Par6, and aPKC Polarity Proteins in Normal Neurodevelopment and in Neurodegenerative and Neuropsychiatric Disorders.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Review
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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

7 authors at 2 institutions in 2 countries.

Jungmook LyuCatholic Institute for Visual Science, Department of Ophthalmology and Visual Science, College of Medicine, The Catholic University of Korea, Seoul 137-040, South Korea; The Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Department of Biochemistry and Molecular Biology, University of Southern California, Keck School of Medicine, Los Angeles, CA 90042, USA. Electronic address: jmlyu@catholic.ac.kr.
Hee-Ryang Kim
Vicky Yamamoto
Si Ho Choi
Zong Wei
Choun-Ki Joo
Wange Lu
University of Southern California · USCatholic University of Korea · KR

Funding

Molecular Mechanisms of Neuronal DifferentiationR01NS067213 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LU, WANGE · 2010 to 2014
$1.7M
NINDS NIH HHS 5R01NS067213NINDS NIH HHS R01 NS067213
6 · The paper itself

Abstract

Neural progenitor cells (NPCs) are multipotent cells that can self-renew and differentiate into neurons and glial cells. However, mechanisms that control their fate decisions are poorly understood. Here, we show that Smek1, a regulatory subunit of the serine/threonine protein phosphatase PP4, promotes neuronal differentiation and suppresses the proliferative capacity of NPCs. We identify the cell polarity protein Par3, a negative regulator of neuronal differentiation, as a Smek1 substrate and demonstrate that Smek1 suppresses its activity. We also show that Smek1, which is predominantly nuclear in NPCs, is excluded from the nucleus during mitosis, allowing it to interact with cortical/cytoplasmic Par3 and mediate its dephosphorylation by the catalytic subunit PP4c. These results identify the PP4/Smek1 complex as a key regulator of neurogenesis.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell Adhesion MoleculesCell CycleCell Cycle ProteinsCell DifferentiationCells, CulturedHEK293 CellsHumansMiceNeural Stem CellsNeurogenesisPhosphoprotein PhosphatasesPhosphorylationProsencephalonSubcellular FractionsAdaptor Proteins, Signal TransducingCell Adhesion MoleculesCell Cycle ProteinsPard3 protein, mousePhosphoprotein PhosphatasesPpp4r3a protein, mouseprotein phosphatase 4

Identifiers

PMID24209749
PMCPMC3855259
OpenAlexW2099840327

What OpenQuestion holds

Textmetadata
LicenceTDM
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.