Peng Mian, Yi Wanhua, Murong Min, Peng Na, Tong Huasheng, Jiang Mengliu, Jin Di, Peng Suliu, Liang Weifen, Quan Jingwen, Li Muman, Shi Linna, Xiao Guizhen
Department of Critical Care Medicine, Shenzhen Luohu Hospital Group, Shenzhen, Guangdong, 518001, China.
Department of Critical Care Medicine, General Hospital of Southern Theater Command, Guangzhou, Guangdong, 510010, China.
Microb Pathog. 2023 Apr;177:106028. doi: 10.1016/j.micpath.2023.106028. Epub 2023 Feb 14.
Heat stress causes an elevation of intestinal epithelial barrier permeability and leads to multiple organ dysfunction in heatstroke. Akkermansia muciniphila (A. muciniphila) plays a role in maintaining intestinal integrity and improving the inflammatory state. This study aimed to investigate whether A. muciniphila could alleviate heat stress-induced dysfunction of intestinal permeability in Caco-2 monolayers and have the preventive effects on heatstroke.
Human intestinal epithelial Caco-2 cells were preincubated with live or pasteurized A. muciniphila then exposed to heat stress at 43 °C. Transepithelial electrical resistance (TEER) and the flux of horseradish peroxidase (HRP) across cell monolayers were measured to determine intestinal permeability. The levels of the tight junction proteins Occludin, ZO-1 and HSP27 were analyzed by Western blotting. These proteins were immunostained and localized by fluorescence microscopy. TJ morphology was observed using transmission electron microscopy (TEM).
Both live and pasteurized A. muciniphila effectively attenuated the decrease in TEER and impairment of intestinal permeability in HRP flux induced by heat exposure. A. muciniphila significantly elevated the expression of Occludin and ZO-1 by promoting HSP27 phosphorylation. The distortion and redistribution of tight junction proteins and disruption of morphology were also effectively prevented by pretreatment with A. muciniphila.
This study indicates for the first time that both live and pasteurized A. muciniphila play an important protective role against heat-induced permeability dysfunction and epithelial barrier damage.
热应激会导致肠道上皮屏障通透性升高,并引发中暑时的多器官功能障碍。嗜黏蛋白阿克曼氏菌(A. muciniphila)在维持肠道完整性和改善炎症状态方面发挥作用。本研究旨在探讨嗜黏蛋白阿克曼氏菌是否能减轻热应激诱导的Caco-2单层细胞肠道通透性功能障碍,并对中暑具有预防作用。
将人肠道上皮Caco-2细胞先用活的或巴氏杀菌的嗜黏蛋白阿克曼氏菌预孵育,然后在43℃下暴露于热应激。测量跨上皮电阻(TEER)和辣根过氧化物酶(HRP)跨细胞单层的通量,以确定肠道通透性。通过蛋白质免疫印迹法分析紧密连接蛋白闭合蛋白(Occludin)、紧密连接蛋白1(ZO-1)和热休克蛋白27(HSP27)的水平。这些蛋白质通过荧光显微镜进行免疫染色和定位。使用透射电子显微镜(TEM)观察紧密连接形态。
活的和巴氏杀菌的嗜黏蛋白阿克曼氏菌均有效减轻了热暴露诱导的TEER降低和HRP通量中肠道通透性的损伤。嗜黏蛋白阿克曼氏菌通过促进HSP27磷酸化显著提高了Occludin和ZO-1的表达。嗜黏蛋白阿克曼氏菌预处理也有效防止了紧密连接蛋白的扭曲和重新分布以及形态破坏。
本研究首次表明,活的和巴氏杀菌的嗜黏蛋白阿克曼氏菌对热诱导的通透性功能障碍和上皮屏障损伤均发挥重要的保护作用。