八胺通过维持Caco2细胞的基底自来减轻肠道屏障损伤
Xiaoli Liu1, Yan Zhou2, Yu Zhang3
1School of Basic Medical Sciences, Binzhou Medical University, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, Shandong 264003, P.R. China.
Molecular medicine reports
|April 5, 2024
概括
八胺通过通过SSTR2维持细胞活性和自,保护肠道屏障功能,这对于预防炎症损伤至关重要.
科学领域:
- 胃肠病学 胃肠病学
- 细胞生物学 细胞生物学
- 分子医学是分子医学.
背景情况:
- 肠道粘膜屏障对内部环境的稳定性至关重要,并与肠道炎症有关.
- 八甲胺 (OCT) 在肠道损伤方面表现有前途,但其机制尚不清楚.
研究的目的:
- 使用体外炎症模型研究Octreotide对肠粘膜屏障功能的保护作用.
- 阐明 somatostatin受体2 (SSTR2) 在 Octreotide 作用机制中的作用.
主要方法:
- 脂聚糖 (LPS) 诱导的炎症细胞模型.
- 细胞计数套件-8测定活力,跨表皮电阻和FITC-dextran 4测定透性.
- 对SSTR2的基因沉默,免疫阻塞,RT-qPCR用于紧密结合蛋白 (zona occludens 1).
- 电子显微镜和LC3-II/LC3-I转换用于自评估.
主要成果:
- 治疗LPS减少了细胞活力,增加了肠道透性,并破坏了紧密的结节 (zona occludens 1).
- 自标志物 (LC3) 在LPS后显示出动态变化.
- 依赖SSTR2的Octreotide治疗恢复了细胞活性,降低了透性,并使紧结蛋白和自正常化.
结论:
- 通过SSTR2介导的奥克特雷奥提德,保护肠道屏障功能.
- OCT维持肠道上皮细胞的基础自和细胞活性,抵消炎症诱导的功能障碍.
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