Literature DB >> 30186504

MicroRNA-126 accelerates IgE-mediated mast cell degranulation associated with the PI3K/Akt signaling pathway by promoting Ca2+ influx.

Yuan Bao1, Song Wang2, Yang Gao2, Wen Zhang3, Haitao Jin4, Yang Yang1, Jiangyu Li5.   

Abstract

Mast cells (MCs) have been reported to serve a crucial role in allergic diseases, including asthma, allergic rhinitis and anaphylaxis. A previous study revealed that microRNA-126 (miR-126) was associated with airway hyperresponsiveness induced by house dust mites, however the molecular mechanisms were unclear. The present study aimed to investigate the effect of miR-126 on immunoglobulin E (IgE)-regulated MC degranulation and explore its underlying mechanisms. miR-126 expression was quantified using a rat model in vivo and in rat peritoneal mast cells (RPMCs) in vitro. Overexpression or downregulation of miR-126 was established by transfection with miR-126 mimics or miR-126 inhibitors and MC degranulation was subsequently evaluated. The effect of miR-126 on protein kinase B (Akt) and phosphorylated Akt protein expression was examined by western blot analysis. The phosphoinositide 3-kinase (PI3K) inhibitor (LY294002) was used to determine the role of the PI3K/Akt signaling pathway. In addition, cytosolic calcium (Ca2+) levels were measured by a fura-2 assay. The results demonstrated that miR-126 expression was upregulated in the ear tissues of rats with allergic contact dermatitis and IgE-activated MCs. The overexpression of miR-126 in RPMCs was established following miR-126 mimic transfection. The release of β-hexosaminidase and histamine, markers of MC degranulation, were significantly increased in cells with miR-126 overexpression. The phosphorylation of Akt was significantly increased following transfection with miR-126 mimics in stimulated cells, however the signaling activation was abrogated by LY294002. In addition, Ca2+ influx was significantly promoted in stimulated RPMCs overexpressing miR-126. These results indicate that miR-126 accelerated IgE-mediated MC degranulation associated with the PI3K/Akt signaling pathway by promoting Ca2+ influx. This suggests that miR-126 may be a promising therapeutic target for the treatment of allergic skin diseases.

Entities:  

Keywords:  Ca2+ influx; allergic skin diseases; mast cells; microRNA-126; phosphoinositide 3-kinase/protein kinase B signaling pathway

Year:  2018        PMID: 30186504      PMCID: PMC6122504          DOI: 10.3892/etm.2018.6510

Source DB:  PubMed          Journal:  Exp Ther Med        ISSN: 1792-0981            Impact factor:   2.447


  32 in total

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7.  Inhibition of miR-25 improves cardiac contractility in the failing heart.

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Review 9.  Genetic and Imaging Approaches Reveal Pro-Inflammatory and Immunoregulatory Roles of Mast Cells in Contact Hypersensitivity.

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Journal:  Front Immunol       Date:  2018-06-05       Impact factor: 7.561

10.  MicroRNA‑126 inhibits proliferation and metastasis by targeting pik3r2 in prostate cancer.

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Journal:  Mol Med Rep       Date:  2015-12-09       Impact factor: 2.952

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