Evidence map›Paper›PMID 24858548›Full record

ArticlePloS one2014

CXC chemokine CXCL12 and its receptor CXCR4 in tree shrews (Tupaia belangeri): structure, expression and function.

Guiyuan Chen, Wei Wang, Shengke Meng, Lichao Zhang, Wenxue Wang, Zongmin Jiang, Min Yu, Qinghua Cui, Meizhang Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Tree shrew (Zoological research · 2017
    Review
  10. Review
  11. Article
  12. 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

9 authors at 3 institutions in 1 country.

Guiyuan ChenDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China; Department of Biochemistry & Molecular Biology, School of Basic Medicine, Dali University, Dali, China.
Wei WangDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China; Department of Rheumatology & Immunology, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Shengke MengDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Lichao ZhangDepartment of Hepatobiliary Surgery, Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Wenxue WangDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Zongmin JiangDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Min YuDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Qinghua CuiDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Meizhang LiDepartment of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming, China.
Yunnan University · CNKunming Medical University · CNDali University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokines are small secreted proteins functionally involved in the immune system's regulation of lymphocyte migration across numerous mammalian species. Given its growing popularity in immunological models, we investigated the structure and function of chemokine CXCL12 protein in tree shrews. We found that CXCL12 and its receptor CXCR4 in tree shrew had structural similarities to their homologous human proteins. Phylogenetic analysis supports the view that tree shrew is evolutionarily-close to the primates. Our results also showed that the human recombinant CXCL12 protein directly enhanced the migration of tree shrew's lymphocytes in vitro, while AMD3100 enhanced the mobilization of hematopoietic progenitor cells (HPCs) from bone marrow into peripheral blood in tree shrew in vivo. Collectively, these findings suggested that chemokines in tree shrews may play the same or similar roles as those in humans, and that the tree shrew is a viable animal model for studying human immunological diseases.

Indexed as

Chemokine CXCL12Models, ImmunologicalPhylogenyReceptors, CXCR4TupaiaAnimalsAnti-HIV AgentsBenzylaminesCyclamsGene Expression RegulationHeterocyclic CompoundsHumansAnti-HIV AgentsBenzylaminesChemokine CXCL12CyclamsHeterocyclic CompoundsplerixaforReceptors, CXCR4

Identifiers

PMID24858548
PMCPMC4032326
OpenAlexW2051300892

What OpenQuestion 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 OpenQuestion graph.