Evidence map›Paper›PMID 31816056›Full record

ArticleThe Journal of cell biology2020

NCAM regulates temporal specification of neural progenitor cells via profilin2 during corticogenesis.

Rui Huang, De-Juan Yuan, Shao Li, Xue-Song Liang, Yue Gao, Xiao-Yan Lan, Hua-Min Qin, Yu-Fang Ma, Guang-Yin Xu, Melitta Schachner and 4 more

Abstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. NCAM mimetic peptide P2 synergizes with bone marrow mesenchymal stem cells in promoting functional recovery after stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Neural glycomics: the sweet side of nervous system functions.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. Review
  13. 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

14 authors.

Rui Huang *Neurology Department, Dalian Municipal Central Hospital affiliated with Dalian Medical University, Dalian, China.
De-Juan Yuan *Jiangsu Key Laboratory of Translational Research and Therapy for Neuro-Psycho-Diseases, Institute of Neuroscience, Soochow University, Suzhou, China.
Shao Li *Physiology Department, Dalian Medical University, Dalian, China.
Xue-Song LiangNeurology Department, Dalian Municipal Central Hospital affiliated with Dalian Medical University, Dalian, China.
Yue GaoNeurology Department, Dalian Municipal Central Hospital affiliated with Dalian Medical University, Dalian, China.
Xiao-Yan LanNeurology Department, Dalian Municipal Central Hospital affiliated with Dalian Medical University, Dalian, China.
Hua-Min QinPathology Department, The Second Hospital of Dalian Medical University, Dalian, China.
Yu-Fang MaBiochemistry and Molecular Biology Department, Dalian Medical University, Dalian, China.
Guang-Yin XuJiangsu Key Laboratory of Translational Research and Therapy for Neuro-Psycho-Diseases, Institute of Neuroscience, Soochow University, Suzhou, China.
Melitta SchachnerCenter for Neuroscience, Shantou University Medical College, Shantou, China.
Vladimir SytnykSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
Johannes BoltzeSchool of Life Sciences, University of Warwick, Coventry, UK.
Quan-Hong MaJiangsu Key Laboratory of Translational Research and Therapy for Neuro-Psycho-Diseases, Institute of Neuroscience, Soochow University, Suzhou, China.
Shen LiNeurology Department, Dalian Municipal Central Hospital affiliated with Dalian Medical University, Dalian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of cerebral cortex requires spatially and temporally orchestrated proliferation, migration, and differentiation of neural progenitor cells (NPCs). The molecular mechanisms underlying cortical development are, however, not fully understood. The neural cell adhesion molecule (NCAM) has been suggested to play a role in corticogenesis. Here we show that NCAM is dynamically expressed in the developing cortex. NCAM expression in NPCs is highest in the neurogenic period and declines during the gliogenic period. In mice bearing an NPC-specific NCAM deletion, proliferation of NPCs is reduced, and production of cortical neurons is delayed, while formation of cortical glia is advanced. Mechanistically, NCAM enhances actin polymerization in NPCs by interacting with actin-associated protein profilin2. NCAM-dependent regulation of NPCs is blocked by mutations in the profilin2 binding site. Thus, NCAM plays an essential role in NPC proliferation and fate decision during cortical development by regulating profilin2-dependent actin polymerization.

Indexed as

Cell DifferentiationNeurogenesisAnimalsCD56 AntigenCell ProliferationCells, CulturedCerebral CortexMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeural Stem CellsNeurogliaNeuronsProfilinsCD56 AntigenNcam1 protein, mouseProfilins

Identifiers

PMID31816056
PMCPMC7039204

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.