N6‐methyladenosine methylation regulator RBM15 promotes the progression of diabetic nephropathy by regulating cell proliferation, inflammation, oxidative stress, and pyroptosis through activating the AGE‐RAGE pathway

Abstract

AbstractBackgroundDiabetic nephropathy (DN) is a major cause of end‐stage renal disease throughout the world, and m6A modification plays a critical role in the progression of DN. We aimed to find m6A‐related genes and their regulatory mechanisms in DN.MethodsThe expression levels of four important m6A‐related genes (METTL16, RBM15, IGF2BP1, and ALKBH5) were detected by quantitative real‐time PCR (RT‐qPCR). RBM15 was chosen and its function was explored. The downstream pathway of RBM15 was screened by transcriptome sequencing. The levels of AGE, inflammation, and oxidative stress were determined with enzyme‐linked immunosorbent assay, and the expression of AGE‐RAGE pathway‐related proteins were detected by Western blot (WB). Cell proliferation was assessed by Cell counting Kit‐8 (CCK‐8). The levels of pyroptosis‐related proteins were evaluated by RT‐qPCR or WB.ResultsMETTL16 and RBM15 were up regulated in the mouse model of DN, in which RBM15 was more significant. Silencing RBM15 recovered cell proliferation, reduced the levels of inflammation factors, and inhibited cell pyroptosis in high glucose‐induced HK‐2 cells. Transcriptome sequencing suggested that the AGE‐RAGE pathway might be downstream of RBM15. RBM15 knockdown reduced AGE level and the expression of AGE‐RAGE pathway‐related proteins. After silencing RBM15, we found that activating the AGE‐RAGE pathway inhibited cell proliferation, increased the levels of inflammation factors, promoted oxidative stress, and induced cell pyroptosis in HK‐2 cell model of DN.ConclusionThe m6A‐related gene RBM15 inhibited cell proliferation, promoted inflammation, oxidative stress, and cell pyroptosis, thereby facilitating the progression of DN through the activation of the AGE‐RAGE pathway.