Evidence map›Paper›PMID 31782037›Full record

ArticleCellular and molecular neurobiology2020

Differential Inhibition of Sox10 Functions by Notch-Hes Pathway.

Guanxiu Xiao, Junqing Du, Huihui Wu, Xinqi Ge, Xiaofeng Xu, Aifen Yang, Ying Zhu, Xuemei Hu, Kang Zheng, Qiang Zhu and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Regulators of Oligodendrocyte Differentiation.Cold Spring Harbor perspectives in biology · 2024
    Review
  4. Conditional Deletion ofInternational journal of molecular sciences · 2023
    Article
  5. Article
  6. 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 2 institutions in 2 countries.

Guanxiu XiaoCollege of Life Sciences, Zhejiang University, Hangzhou, 310036, China.
Junqing DuInstitute of Life Sciences, Key Laboratory of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 310036, China.
Huihui WuInstitute of Life Sciences, Key Laboratory of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 310036, China.
Xinqi GeCollege of Life Sciences, Zhejiang University, Hangzhou, 310036, China.
Xiaofeng XuInstitute of Life Sciences, Key Laboratory of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 310036, China.
Aifen YangInstitute of Life Sciences, Key Laboratory of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 310036, China.
Ying ZhuDepartment of Anatomical Sciences and Neurobiology, School of Medicine, University of Louisville, Louisville, KY, 40292, USA.
Xuemei HuDepartment of Anatomical Sciences and Neurobiology, School of Medicine, University of Louisville, Louisville, KY, 40292, USA.
Kang ZhengInstitute of Life Sciences, Key Laboratory of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 310036, China.
Qiang ZhuDepartment of Anatomical Sciences and Neurobiology, School of Medicine, University of Louisville, Louisville, KY, 40292, USA.
Mengsheng QiuCollege of Life Sciences, Zhejiang University, Hangzhou, 310036, China. m0qiu001@yahoo.com.ORCID http://orcid.org/0000-0001-6038-3718
Hangzhou Normal University · CNUniversity of Louisville · US

Funding

National Natural Science Foundation of China 31572224National Natural Science Foundation of China 31771621Natural Science Foundation of Zhejiang Province LQ16C090004
6 · The paper itself

Abstract

In the developing central nervous system, the terminal differentiation of oligodendrocytes (OLs) is regulated by both extrinsic and intrinsic factors. Recent studies have suggested that the Notch-Hes signaling pathway influences the maturation of oligodendrocytes in culture and during development. However, the specific Notch receptors and their downstream effectors Hes genes that are involved in oligodendrocyte maturation have not been investigated systematically. In this study, we showed that Notch1 and Notch3 are expressed in oligodendrocyte precursor cells (OPCs) during gliogenesis, and Hes5 is the major Notch downstream transcription factor that is transiently expressed in OPCs. Overexpression of Notch intracellular domain (NICD) and Hes5 proteins in embryonic chicken spinal cord suppressed both the endogenous and Sox10-induced Mbp gene expression. Unexpectedly, overexpression of NICD/Hes5 did not inhibit Sox10 induction of Olig2 expression and Myrf induced Mbp expression, suggesting the differential inhibitory effects of NICD/Hes5 signaling on Sox10 activation of myelin-related genes and early progenitor genes.

Indexed as

Signal TransductionAnimalsBasic Helix-Loop-Helix ProteinsChickensGene Expression Regulation, DevelopmentalMice, KnockoutMyelin Basic ProteinOligodendrogliaReceptors, NotchSOXE Transcription FactorsSpinal CordStem CellsBasic Helix-Loop-Helix ProteinsMyelin Basic ProteinReceptors, NotchSOXE Transcription FactorsDifferentiationExpression patternHes5Oligodendrocytes

Identifiers

PMID31782037
PMCPMC11448864
OpenAlexW2991047085

What OpenQuestion holds

Textmetadata
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.