Evidence map›Paper›PMID 27587248›Full record

ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2016

[Effect of miR- 155 on immune- factors and its mechanism in mesenchymal stem cells under hypoxic environment].

X Han, H Bai, J J Yin, K Yang, Y X Han, J F Ou, C B Wang, T Wu

Open access · greenAbstract read
In one paragraph

Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

X HanDepartment of Hematology, Center for Hematologic Diseases of Chinese PLA/Lanzhou Military Area General Hospital, Lanzhou 730050, China.
H Bai
J J Yin
K Yang
Y X Han
J F Ou
C B Wang
T Wu
Lanzhou Army General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of miR-155 on immune-factors and its mechanism in mesenchymal stem cells under hypoxia.

methodsThe microRNA sequences targeting miR-155 mimic and mimic NC gene was designed and transfected into MSC by lipofectamineTM 2000. Lipopolysaccharide was used to stimulate the immunity of MSC under hypoxic environment. Transfection efficiency of miR- 155 and immune-related genes (IL-6, IL-8, iNOS, TGF-β, HIF-1α) were detected by real-time RT-PCR. The cell surface antigens (CD29, CD73, CD90, CD105, CD31, CD45) and supernatant cytokines (IL- 6, IL- 8, TGF- β, SDF- 1α) were analyzed by flow cytometry and ELISA, respectively. Western Blot was applied to evaluate related proteins, iNOS and HIF- 1α.

resultmiR- 155 was transfected into MSC effectively (53.447±8.361 vs 1.070±0.174, P<0.01). In miR-155 high-expressed groups, the expressions of IL-6 and IL-8 were up-regulated [(24.201±1.536) vs (1.802±0.058), P<0.01; (24.406±4.611) vs (7.407± 1.553), P<0.01] and iNOS was markedly suppressed [(0.151 ±0.035) vs (32.925±1.632), P<0.01]. Hypoxia up-regulated expressions of HIF-1α [(45.093±3.371) vs (2.210±0.498), P<0.01] and promoted the regulation of miR-155. MiR-155 and hypoxia had effect on mRNA expression of SDF-1α and TGF-β [(5.690±1.655) vs (0.841±0.194), P<0.01; (6.982±1.353) vs (0.632±0.184), P<0.01]. However, there was no influence on cytokines of SDF- 1α and TGF- β [(24.609±2.584) vs (25.359±2.455), P=0.760;(0.568±0.019) vs (0.345±0.037), P=0.002].

conclusionHypoxia environment may promote miR-155 to positively modulate immune factors of MSC through up-regulating the expression of HIF-1α, which down-regulated iNOS protein.

Indexed as

Cell HypoxiaChemokine CXCL12Down-RegulationHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitImmunologic FactorsInterleukin-6LipidsMesenchymal Stem CellsMicroRNAsReal-Time Polymerase Chain ReactionTransfectionTransforming Growth Factor betaUp-RegulationChemokine CXCL12Hypoxia-Inducible Factor 1, alpha SubunitImmunologic FactorsInterleukin-6LipidsLipofectamineMicroRNAsMIRN155 microRNA, humanTransforming Growth Factor beta

Identifiers

PMID27587248
PMCPMC7348527
OpenAlexW2523996045

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.