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在糖尿病肾病中,通过靶向 导致足细胞损伤和自噬障碍加重。

deficiency exacerbates podocyte injury and autophagy disorder by targeting in diabetic nephropathy.

机构信息

Department of Nephropathy, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, PR China.

Center for Scientific Research, Anhui Medical University, Hefei, Anhui, PR China.

出版信息

Autophagy. 2024 May;20(5):1072-1097. doi: 10.1080/15548627.2023.2286128. Epub 2023 Dec 5.

Abstract

Circular RNAs (circRNAs) are special non-coding RNA (ncRNA) molecules that play a significant role in many diseases. However, the biogenesis and regulation of circRNAs in diabetic nephropathy (DN) are largely unknown. Here, we investigated the expression profile of circRNAs in kidney of DN mice through circular RNA sequencing (circRNA-seq). The renal biopsy samples of patients with DN had low expression, which was significantly associated with renal function. Furthermore, loss-of-function and gain-of-function experiments were carried out to prove the role of in DN. Podocyte conditional knockin (cKI) or systemic overexpression of alleviated albuminuria and restored macroautophagy/autophagy in kidney of diabetic mice. However, knockdown exacerbated albuminuria and podocyte injury. Mechanistically, we found directly binds to to perform its function. Silencing of or overexpression of recovered podocyte autophagy both and . To examine the cause of downregulation in DN, bioinformatics prediction found that sequence has a high possibility of containing an m6A methylation site. Additionally, METTL3 was proved to regulate the expression and methylation level of through YTHDF2 (YTH N6-methyladenosine RNA binding protein 2). In conclusion, this study revealed that regulates podocyte autophagy by targeting in DN. Therefore, is a potential biomarker for prevention and cure of DN. CCL2/MCP-1: C-C motif chemokine ligand 2; ceRNA: competing endogenous RNA; circRNA: circular RNA; cKI: conditional knockin; cKO: conditional knockout; CRE: creatinine; DM: diabetes mellitus; DN: diabetic nephropathy; ESRD: end-stage renal disease; HG: high glucose; IF: immunofluorescence; MAP1LC3/LC3B: microtubule-associated protein 1 light chain 3 beta; MPC5: mouse podocyte clone 5; MTECs: mouse tubular epithelial cells; MTOR: mechanistic target of rapamycin kinase; NC: normal control; ncRNA: non-coding RNA; NPHS1: nephrosis 1, nephrin; NPHS2: nephrosis 2, podocin; PAS: periodic acid-Schiff; RELA/p65: v-rel reticuloendotheliosis viral oncogene homolog A (avian); SDs: slit diaphragm proteins; Seq: sequencing; STZ: streptozotocin; SV40: SV40-MES13-cells, mouse mesangial cell line; T1D: type 1 diabetes mellitus; T2D: type 2 diabetes mellitus; TEM: transmission electron microscopy; TNF/TNF-α: tumor necrosis factor; VECs: vascular endothelial cells; WT1: WT1 transcription factor; YTHDF2: YTH N6-methyladenosine RNA binding protein 2.

摘要

环状 RNA(circRNAs)是一类特殊的非编码 RNA(ncRNA)分子,在许多疾病中发挥着重要作用。然而,糖尿病肾病(DN)中 circRNAs 的生物发生和调控机制在很大程度上尚不清楚。在这里,我们通过环状 RNA 测序(circRNA-seq)研究了 DN 小鼠肾脏中 circRNAs 的表达谱。DN 患者的肾活检样本中 表达水平较低,与肾功能显著相关。此外,还进行了功能丧失和获得功能实验,以证明 在 DN 中的作用。条件敲入(cKI)或系统过表达 可减轻糖尿病小鼠的白蛋白尿并恢复肾脏中的巨自噬/自噬。然而, 敲低则加剧了白蛋白尿和足细胞损伤。机制上,我们发现 直接与 结合以发挥其功能。沉默 或过表达 均可恢复 和 。为了研究 在 DN 中下调的原因,生物信息学预测发现 序列极有可能含有 m6A 甲基化位点。此外,METTL3 通过 YTHDF2(YTH N6-甲基腺苷 RNA 结合蛋白 2)被证明可调节 的表达和甲基化水平。综上所述,本研究揭示了 在 DN 中通过靶向 来调节足细胞自噬。因此, 是预防和治疗 DN 的潜在生物标志物。CCL2/MCP-1:C-C 基序趋化因子配体 2;ceRNA:竞争性内源性 RNA;circRNA:环状 RNA;cKI:条件敲入;cKO:条件敲除;CRE:肌酐;DM:糖尿病;DN:糖尿病肾病;ESRD:终末期肾病;HG:高葡萄糖;IF:免疫荧光;MAP1LC3/LC3B:微管相关蛋白 1轻链 3B;MPC5:小鼠足细胞克隆 5;MTECs:小鼠肾小管上皮细胞;MTOR:雷帕霉素靶蛋白激酶;NC:正常对照;ncRNA:非编码 RNA;NPHS1:肾病 1,nephrin;NPHS2:肾病 2,podocin;PAS:过碘酸-Schiff;RELA/p65:v-rel 网状内皮增生病毒癌基因同源物 A(禽);SDs:裂孔隔膜蛋白;Seq:测序;STZ:链脲佐菌素;SV40:SV40-MES13 细胞,小鼠系膜细胞系;T1D:1 型糖尿病;T2D:2 型糖尿病;TEM:透射电子显微镜;TNF/TNF-α:肿瘤坏死因子;VECs:血管内皮细胞;WT1:WT1 转录因子;YTHDF2:YTH N6-甲基腺苷 RNA 结合蛋白 2。

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