Evidence map›Paper›PMID 26549736›Full record

ArticleImmunology letters2016

MiR-150 impairs inflammatory cytokine production by targeting ARRB-2 after blocking CD28/B7 costimulatory pathway.

Wei Sang, Ying Wang, Cong Zhang, Dianzheng Zhang, Cai Sun, Mingshan Niu, Zhe Zhang, Xiangyu Wei, Bin Pan, Wei Chen and 4 more

Abstract read
In one paragraph

Article in Immunology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 59 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

14 authors at 5 institutions in 2 countries.

Wei SangThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Ying WangThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Cong ZhangDepartment of Hematology, Huaibei Miners General Hospital, Anhui Province, China.
Dianzheng ZhangDepartment of Biochemistry and Molecular Biology, Philadelphia College of Osteopathic Medicine, USA.
Cai SunThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Mingshan NiuThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Zhe ZhangThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Xiangyu WeiThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Bin PanThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Wei ChenThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Dongmei YanThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Lingyu ZengThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China.
Thomas P LoughranDepartment of Medicine, University of Virginia Cancer Center, VA, USA. Electronic address: tploughran@virginia.edu.
Kailin XuThe Key Laboratory of Transplantation Immunity, Affiliated Hospital of Xuzhou Medical College, Jiangsu Province, China. Electronic address: kailinxu616@126.com.
Affiliated Hospital of Xuzhou Medical College · CNXuzhou Medical College · CNHuaibei Mining (China) · CNPhiladelphia College of Osteopathic Medicine · USUniversity of Virginia Cancer Center

Funding

Survival Mechanisms in Leukemic NK CellsR01CA098472 · NCI · UNIVERSITY OF VIRGINIA · PI LOUGHRAN, THOMAS P. · 2003 to 2016
$4.0M
NCI NIH HHS R01 CA098472
6 · The paper itself

Abstract

MiR-150, a major modulator negatively regulating the development and differentiation of various immune cells, is widely involved in orchestrating inflammation. In transplantation immunity, miR-150 can effectively induce immune tolerance, although the underlying mechanisms have not been fully elucidated. In the current study, we found that miR-150 is elevated after blocking CD28/B7 co-stimulatory signaling pathway and impaired IL-2 production by targeting ARRB2. Further investigation suggested that miR-150 not only repressed the level of ARRB2/PDE4 directly but also prevented AKT/ARRB2/PDE4 trimer recruitment into the lipid raft by inhibiting the activities of PI3K and AKT through the cAMP-PKA-Csk signaling pathway. This leads to the interruption of cAMP degradation and subsequently results in inhibition of the NF-kB pathway and reduced production of both IL-2 and TNF. In conclusion, our study demonstrated that miR-150 can effectively prevent CD28/B7 co-stimulatory signaling transduction, decrease production of inflammatory cytokines, such as IL-2 and TNF, and elicit the induction of immune tolerance. Therefore, miR-150 could become a novel potential therapeutic target in transplantation immunology.

Indexed as

B7 Antigensbeta-Arrestin 2CD28 AntigensCD4-Positive T-LymphocytesCells, CulturedCyclic AMPHumansImmune ToleranceInflammation MediatorsInterleukin-2Membrane MicrodomainsMicroRNAsNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionARRB2 protein, humanB7 Antigensbeta-Arrestin 2CD28 AntigensCyclic AMPInflammation MediatorsInterleukin-2MicroRNAsMIR150, humanNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTumor Necrosis Factor-alphaCD28/B7 co-stimulatory signaling pathwayInflammatory cytokineMicroRNAT cell

Identifiers

PMID26549736
PMCPMC4846526
OpenAlexW2120346550

What OpenQuestion holds

Textmetadata
LicenceTDM
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.