From the Department of Gastroenterology, Central Hospital of Shanxian, Heze.
Department of Gastroenterology, The Second People's Hospital of Jingmen, Jingmen, China.
Pancreas. 2021 Feb 1;50(2):243-250. doi: 10.1097/MPA.0000000000001748.
This research plans to address the function of miR-204-5p/tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma (YWHAG) in cerulein-induced acute pancreatitis (AP).
Rat pancreatic acinar cell AR42J was stimulated by 100 nmol/L of cerulein to mimic the situation in AP. Gene Expression Omnibus database was used to select differentially expressed genes. StarBase database and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were used to select the target genes of miR-204-5p, which were further affirmed by dual luciferase assay. The biological behaviors of AR42J cells were measured by cell proliferation and flow cytometry assays. Quantitative real-time polymerase chain reaction and western blot assays were executed to assess YWHAG expression. The secretion of C-C Motif Chemokine Ligand 2/Timp metallopeptidase inhibitor 1 in AR42J cells was evaluated by enzyme-linked immunosorbent assay. The protein expression of YAP1/p-YAP1/PI3K/p-PI3K was measured by western blot.
miR-204-5p expression was profoundly reduced in cerulein-induced AP model. YWHAG was upregulated in cerulein-induced AP model and related to C-C Motif Chemokine Ligand 2/Timp1. In addition to the negative association between miR-204-5p and YWHAG, the alleviation impact of miR-204-5p mimic on cerulein-induced AR42J cell damage was blocked by YWHAG overexpression and PI3K/Hippo signaling pathways activation.
These observations indicated that the alleviation impact of miR-204-5p on cerulein-induced AR42J cell damage was mediated via YWHAG and PI3K/Hippo signaling pathways.
本研究旨在探讨 miR-204-5p/酪氨酸 3-单加氧酶/色氨酸 5-单加氧酶激活蛋白γ(YWHAG)在鹅膏蕈碱诱导的急性胰腺炎(AP)中的作用。
用 100 nmol/L 鹅膏蕈碱刺激大鼠胰腺腺泡细胞 AR42J,模拟 AP 情况。使用基因表达综合数据库(GEO)数据库筛选差异表达基因。StarBase 数据库和京都基因与基因组百科全书(KEGG)富集分析用于筛选 miR-204-5p 的靶基因,进一步通过双荧光素酶报告基因实验验证。通过细胞增殖和流式细胞术实验检测 AR42J 细胞的生物学行为。实时定量聚合酶链反应(qRT-PCR)和蛋白质印迹实验检测 YWHAG 的表达。酶联免疫吸附实验(ELISA)检测 AR42J 细胞中 C-C 基序趋化因子配体 2/金属蛋白酶组织抑制剂 1 的分泌。蛋白质印迹法(western blot)检测 YAP1/p-YAP1/PI3K/p-PI3K 的蛋白表达。
miR-204-5p 在鹅膏蕈碱诱导的 AP 模型中表达显著下调。YWHAG 在鹅膏蕈碱诱导的 AP 模型中上调,与 C-C 基序趋化因子配体 2/Timp1 相关。miR-204-5p 与 YWHAG 呈负相关,miR-204-5p 模拟物减轻鹅膏蕈碱诱导的 AR42J 细胞损伤的作用被 YWHAG 过表达和 PI3K/Hippo 信号通路激活所阻断。
这些结果表明,miR-204-5p 通过 YWHAG 和 PI3K/Hippo 信号通路减轻鹅膏蕈碱诱导的 AR42J 细胞损伤。