miR-146a modulates TLR1/2 and 4 induced inflammation and links it with proliferation and lipid production via the indirect regulation of GNG7 in human SZ95 sebocytes

Author:

Dull Katalin,Fazekas Fruzsina,Deák Dávid,Kovács Dóra,Póliska Szilárd,Szegedi Andrea,Zouboulis Christos C.,Törőcsik Dániel

Abstract

AbstractActivation of Toll-like receptors (TLR) 1/2 and 4 are central in inducing inflammation in sebocytes by regulating the expression of protein coding mRNAs, however the microRNA (miRNA) profile in response to TLR activation and thus the possible role of miRNAs in modulating sebocyte functions has not been elucidated. In this work we identified miR-146a to have the highest induction in the TLR1/2 and 4 activated SZ95 sebocytes and found that its increased levels led to the down-regulation of IL-8 secretion, decreased the chemoattractant potential and stimulated the proliferation of sebocytes. Assessing the gene expression profile of SZ95 sebocytes treated with a miR-146a inhibitor, the induction of GNG7 was one of the highest, while when cells were treated with a miR-146a mimic, the expression of GNG7 was down-regulated. These findings correlated with our in situ hybridization results, that compared with control, miR-146a showed an increased, while GNG7 a decreased expression in sebaceous glands of acne samples. Further studies revealed, that when inhibiting the levels of GNG7 in SZ95 sebocytes, cells increased their lipid content and decreased their proliferation. Our findings suggest, that miR-146a could be a potential player in acne pathogenesis by regulating inflammation, inducing proliferation and, through the indirect down-regulation of GNG7, promoting the lipid production of sebocytes.

Funder

European Regional Development Fund

Doctoral School of Health Sciences, University of Debrecen

Hungarian National Research, Development and Innovation Funds

European Social Fund

New National Excellence Program of the Ministry of Human Capacities

Bolyai János Research Scholarship of the Hungarian Academy of Sciences

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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