Downregulation of miR‑214-3p attenuates mesangial hypercellularity by targeting PTEN‑mediated JNK/c-Jun signaling in IgA nephropathy
| Autor: | Guochun Chen, Du Yuan, Yan Li, Ming Xia, Chang Wang, Hong Liu, Yu Liu, Liang Peng, Haiyang Liu |
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| Rok vydání: | 2021 |
| Předmět: |
Cell signaling
mesangial cell proliferation PTEN MAP Kinase Kinase 4 MAP Kinase Signaling System Proto-Oncogene Proteins c-jun Renal cortex Mesangial hypercellularity urologic and male genital diseases Applied Microbiology and Biotechnology JNK/c-Jun signaling Random Allocation Downregulation and upregulation medicine Animals miR-214 Molecular Biology Ecology Evolution Behavior and Systematics Mice Inbred BALB C biology Mesangial cell Chemistry PTEN Phosphohydrolase Glomerulonephritis IGA Cell Biology IgA nephropathy Cell cycle MicroRNAs medicine.anatomical_structure Mesangial Cells Cancer research biology.protein miR‑214-3p Female Developmental Biology Research Paper |
| Zdroj: | International Journal of Biological Sciences |
| ISSN: | 1449-2288 |
| Popis: | Mesangial cell (MC) proliferation and matrix expansion are basic pathological characteristics of IgA nephropathy (IgAN). However, the stepwise mechanism of MC proliferation and the exact set of related signaling molecules remain largely unclear. In this study, we found a significant upregulation of miR-214-3p in the renal cortex of IgAN mice by miRNA sequencing. In situ hybridization analysis showed that miR-214-3p expression was obviously elevated in MCs in the renal cortex in IgAN. Functionally, knockdown of miR-214-3p alleviated mesangial hypercellularity and renal lesions in IgAN mice. In vitro, the inhibition of miR-214-3p suppressed MC proliferation and arrested G1-S cell cycle pSrogression in IgAN. Mechanistically, a luciferase reporter assay verified PTEN as a direct target of miR-214-3p. Downregulation of miR-214-3p increased PTEN expression and reduced p-JNK and p-c-Jun levels, thereby inhibiting MC proliferation and ameliorating renal lesions in IgAN. Moreover, these changes could be attenuated by co-transfection with PTEN siRNA. Collectively, these results illustrated that miR-214-3p accelerated MC proliferation in IgAN by directly targeting PTEN to modulate JNK/c-Jun signaling. Therefore, miR-214-3p may represent a novel therapeutic target for IgAN. |
| Databáze: | OpenAIRE |
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