Evidence map›Paper›PMID 28344005›Full record

ArticleStem cell reports2017

miR-342-5p Regulates Neural Stem Cell Proliferation and Differentiation Downstream to Notch Signaling in Mice.

Fang Gao, Yu-Fei Zhang, Zheng-Ping Zhang, Luo-An Fu, Xiu-Li Cao, Yi-Zhe Zhang, Chen-Jun Guo, Xian-Chun Yan, Qin-Chuan Yang, Yi-Yang Hu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 58 citations in OpenAlex.

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  17. MicroRNA Signatures of the Developing Primate Fovea.Frontiers in cell and developmental biology · 2021
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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

16 authors at 3 institutions in 1 country.

Fang GaoDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China; Institute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Yu-Fei ZhangDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Zheng-Ping ZhangDepartment of Spinal Surgery, Honghui Hospital, Xi'an Jiaotong University College of Medicine, Xi'an 710054, China.
Luo-An FuDepartment of Neurosurgery, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Xiu-Li CaoDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Yi-Zhe ZhangDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Chen-Jun GuoDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Xian-Chun YanDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Qin-Chuan YangDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China; Institute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Yi-Yang HuDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Xiang-Hui ZhaoInstitute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Ya-Zhou WangInstitute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Sheng-Xi WuInstitute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Gong JuInstitute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China. Electronic address: jugong@fmmu.edu.cn.
Min-Hua ZhengDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China. Electronic address: minhua_zheng@126.com.
Hua HanDepartment of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China. Electronic address: huahan@fmmu.edu.cn.
Air Force Medical University · CNXi'an Honghui Hospital · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notch signaling is critically involved in neural development, but the downstream effectors remain incompletely understood. In this study, we cultured neurospheres from Nestin-Cre-mediated conditional Rbp-j knockout (Rbp-j cKO) and control embryos and compared their miRNA expression profiles using microarray. Among differentially expressed miRNAs, miR-342-5p showed upregulated expression as Notch signaling was genetically or pharmaceutically interrupted. Consistently, the promoter of the miR-342-5p host gene, the Ena-vasodilator stimulated phosphoprotein-like (Evl), was negatively regulated by Notch signaling, probably through HES5. Transfection of miR-342-5p promoted the differentiation of neural stem cells (NSCs) into intermediate neural progenitors (INPs) in vitro and reduced the stemness of NSCs in vivo. Furthermore, miR-342-5p inhibited the differentiation of neural stem/intermediate progenitor cells into astrocytes, likely mediated by targeting GFAP directly. Our results indicated that miR-342-5p could function as a downstream effector of Notch signaling to regulate the differentiation of NSCs into INPs and astrocytes commitment.

Indexed as

Cell ProliferationNeurogenesisSignal TransductionAnimalsAstrocytesGene Expression RegulationGlial Fibrillary Acidic ProteinMiceMicroRNAsNeural Stem CellsReceptors, NotchGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseMicroRNAsMirn342 microRNA, mouseReceptors, Notchgliaintermediate neural progenitorsmiR-342-5pneural stem cellsneuronNotchRBP-J

Identifiers

PMID28344005
PMCPMC5390133
OpenAlexW2598900420

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.