Evidence map›Paper›PMID 27573194›Full record

ArticleCurrent molecular medicine2016

CXCR7 Participates in CXCL12-mediated Cell Cycle and Proliferation Regulation in Mouse Neural Progenitor Cells.

Y Wang, P Xu, L Qiu, M Zhang, Y Huang, J C Zheng

Open access · bronzeAbstract read
In one paragraph

Article in Current molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed, 32 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

6 authors at 3 institutions in 2 countries.

Y Wang
P Xu
L Qiu
M Zhang
Y HuangShanghai Tenth People's Hospital Affiliated to Tongji University School of Medicine, Shanghai 200072, China; 985930 University of Nebraska Medical Center, Omaha, NE 68198-5930, USA. yhuan1@unmc.edu.
J C Zheng
Tongji University · CNUniversity of Nebraska Medical Center · USShanghai Tenth People's Hospital · CN

Funding

TRAIL and glutaminase: neurotoxic link in HIV-1 DementiaR01NS041858 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZHENG, JIALIN CHARLES · 2001 to 2014
$4.4M
Glutaminase and its neurotoxic link to HANDR01NS097195 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GENDELMAN, HOWARD E · 2016 to 2020
$1.5M
Glutaminase and its neurotoxic link to HANDR56NS041858 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZHENG, JIALIN CHARLES · 2015 to 2015
$376k
Targeting FOX03a with TIC10 to eradicate HIV-1 from CNS reservoirsR03NS094071 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HUANG, YUNLONG · 2015 to 2016
$151k
NINDS NIH HHS R01 NS041858NINDS NIH HHS R01 NS097195NINDS NIH HHS R03 NS094071NINDS NIH HHS R56 NS041858
6 · The paper itself

Abstract

backgroundCell cycle regulation of neural progenitor cells (NPCs) is an essential process for neurogenesis, neural development, and repair after brain trauma. Stromal cell-derived factor-1 (SDF-1, CXCL12) and its receptors CXCR4 and CXCR7 are well known in regulating the migration and survival of NPCs. The effects of CXCL12 on NPCs proliferation, cell cycle regulation, and their associated signaling pathways remain unclear. Cyclin D1 is a protein required for progression through the G1 phase of the cell cycle and a known downstream target of β -catenin. Therefore, cyclin D1 plays critical roles of cell cycle regulation, proliferation, and survival in NPCs.

methodsPrimary mouse NPCs (mNPCs) were derived from brain tissues of wild-type, Cxcr4 knockout, or Cxcr7 knockout mice at mouse embryonic day 13.5 (E13.5). Flow cytometry was used to perform cell cycle analysis by quantitation of DNA content. Real-time PCR and Western blot were used to evaluate mRNA and protein expressions, respectively. Ki67 immunostaining and TUNEL assay were used to assess the proliferation and survival of mNPCs, respectively.

resultsCXCL12 pretreatment led to the shortening of G0/G1 phase and lengthening of S phase, suggesting that CXCL12 regulates cell cycle progression in mNPCs. Consistently, CXCL12 treatment increased the expression of CyclinD1 and β -catenin, and promoted proliferation and survival of mNPCs. Cxcr7 knockout of mNPCs blocked CXCL12-mediated mNPCs proliferation, whereas Cxcr4 knockout mNPC did not significantly effect CXCL12- mediated mNPCs proliferation.

conclusionCXCR7 plays an important role in CXCL12-mediated mNPC cell cycle regulation and proliferation.

Indexed as

Cell CycleAnimalsApoptosisbeta CateninCell ProliferationCell SurvivalChemokine CXCL12Cyclin D1Gene Expression RegulationMiceNeural Stem CellsReceptors, CXCRSignal Transductionbeta CateninChemokine CXCL12Cmkor1 protein, mouseCyclin D1Receptors, CXCR

Identifiers

PMID27573194
PMCPMC5345320
OpenAlexW2507875362

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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.