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microRNA‐146a downregulates IL‐17 and IL‐35 and inhibits proliferation of human periodontal ligament stem cells
Author(s) -
Zhao Sen,
Cheng Yawei,
Kim Jong Ghee
Publication year - 2019
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.28659
Subject(s) - periodontal fiber , microrna , microbiology and biotechnology , periodontal ligament stem cells , stem cell , chemistry , cancer research , medicine , biology , dentistry , gene , biochemistry , alkaline phosphatase , enzyme
Periodontitis is characterized by increased levels of proinflammatory factors, such as interleukin‐17 (IL‐17) and IL‐35. In this study, the expression of microRNA‐146a (miRNA‐146a), IL‐17, and IL‐35 in the plasma of patients with periodontitis and healthy controls were detected by quantitative reverse transcription polymerase chain reaction and enzyme‐linked immunosorbent assay, respectively. miRNA‐146a mimic was transfected into periodontal ligament stem cells (PDLSCs) isolated from periodontitis‐affected teeth and healthy teeth. Cell proliferation and expression of IL‐17 and IL‐35 were detected by cell counting kit‐8 assay and Western blot analysis, respectively. It was observed that miRNA‐146a was downregulated but IL‐17 and IL‐35 were upregulated in the plasma of patients with periodontitis than in healthy controls. miRNA‐146a was inversely correlated with IL‐17 and IL‐35 in patients with periodontitis. miRNA‐146a overexpression inhibited proliferation of PDLSCs derived from both periodontitis‐affected teeth and healthy teeth. miRNA‐146a overexpression led to downregulated IL‐17 and IL‐35 expression in PDLSCs isolated from periodontitis‐affected teeth. We, therefore, conclude that miRNA‐146a may improve periodontitis by downregulating IL‐17 and IL‐35 expression and inhibiting proliferation of human PDLSCs.