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MicroRNA-31 Negatively Regulates Interleukin-34 Expression In Vitro.

Miaomiao LiYang DongZhangming ChenLei MengXingyun LiuXinhui ZhangHuimin WangWeijia MaoJie ZhangZhe JiangTing HuangJie HuPanquan LuoHeinrich KornerSongcheng YingJun Li
Published in: Immunological investigations (2019)
Interleukin-34 (IL-34) is a recently discovered cytokine that promotes tissue macrophage maturation and differentiation. We previously found that 1α,25-Dihydroxyvitamin D3 up-regulated IL-34 expression in SH-SY5Y neural cells. However, whether microRNA regulates IL-34 expression is not completely clear. By using on-line TargetScan and MiRanda software, we found that there was only one conserved microRNA-31 (miR-31) binding site in the 3' untranslated region (3'UTR) of IL-34 mRNA. Intriguingly, using qPCR we demonstrated that miR-31 levels were negatively correlated to IL-34 mRNA levels in different cell lines. By examining the effect of miR-31 on IL-34 3' UTR reporter luciferase activity and on IL-34 mRNA and argonaute RISC catalytic component 2 (AGO2) binding, it was found that miR-31 bound directly to IL-34 3'UTR and regulated the post-transcriptional expression of IL-34 in MGC-803 cells. Moreover, a miR-31 mimic significantly reduced IL-34 expression levels while a miR-31 inhibitor up-regulated IL-34 expression in KYSE-45 and HT-29 cells. Taken together, these results show that miR-31 negatively regulates IL-34 expression by directly binding to the IL-34 3' UTR in vitro.
Keyphrases
  • poor prognosis
  • long non coding rna
  • cell proliferation
  • binding protein
  • long noncoding rna
  • induced apoptosis
  • transcription factor
  • gene expression
  • endoplasmic reticulum stress
  • heat shock