Evidence map›Paper›PMID 37373471›Full record

ArticleInternational journal of molecular sciences2023

CCN3/NOV Regulates Proliferation and Neuronal Differentiation in Mouse Hippocampal Neural Stem Cells via the Activation of the Notch/PTEN/AKT Pathway.

Yan Luan, Hanyue Zhang, Kaige Ma, Yingfei Liu, Haixia Lu, Xinlin Chen, Yong Liu, Zhichao Zhang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Yan LuanInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Hanyue ZhangInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Kaige MaInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Yingfei LiuInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Haixia LuInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Xinlin ChenInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Yong LiuInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.
Zhichao ZhangInstitute of Neurobiology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China.ORCID 0000-0001-7990-101X
Xi'an Jiaotong University · CN

Funding

Fundamental Research Funds for the Central Universities xzy012022035Key Research and Development Projects of Shaanxi Province 2023-YBSF-303National Natural Science Foundation of China 82001493National Natural Science Foundation of China 82171308National Natural Science Foundation of China 82271200
6 · The paper itself

Abstract

Neural stem cells (NSCs) persist in the subgranular zone (SGZ) throughout the lifespan and hold immense potential for the repair and regeneration of the central nervous system, including hippocampal-related diseases. Several studies have demonstrated that cellular communication network protein 3 (CCN3) regulates multiple types of stem cells. However, the role of CCN3 in NSCs remains unknown. In this study, we identified CCN3 expression in mouse hippocampal NSCs and observed that supplementing CCN3 improved cell viability in a concentration-dependent manner. Additionally, in vivo results showed that the injection of CCN3 in the dentate gyrus (DG) increased Ki-67- and SOX2-positive cells while decreasing neuron-specific class III beta-tubulin (Tuj1) and doublecortin (DCX)-positive cells. Consistently with the in vivo results, supplementing CCN3 in the medium increased the number of BrdU and Ki-67 cells and the proliferation index but decreased the number of Tuj1 and DCX cells. Conversely, both the in vivo and in vitro knockdown of the

Indexed as

Nephroblastoma Overexpressed ProteinNeural Stem CellsProto-Oncogene Proteins c-aktAnimalsCell DifferentiationCell ProliferationHippocampusKi-67 AntigenMiceNeurogenesisCcn3 protein, mouseKi-67 AntigenNephroblastoma Overexpressed ProteinProto-Oncogene Proteins c-aktCCN3differentiationhippocampal neural stem cellsNotch/PTEN/AKT pathwayproliferation

Identifiers

PMID37373471
PMCPMC10299577
OpenAlexW4381165523

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.