Lin Rong, Jiang Ye, Zhao Xin Yan, Guan Yang, Qian Wei, Fu Xiao Chao, Ren Hun Yu, Hou Xiao Hua
Division of Gastroenterology, Union Hospital, Wuhan, Hubei Province, China.
J Dig Dis. 2014 Nov;15(11):597-605. doi: 10.1111/1751-2980.12179.
To investigate the influence of gut microbiota on autophagy activation in intestinal epithelial cells (IEC) and to evaluate the IEC autophagy response to different types of Bifidobacteria.
IEC-18 cells were treated with lipopolysaccharide (LPS) derived from enteropathogenic Escherichia coli (EPEC) O127:B8 and culture medium supernatants of four types of Bifidobacteria. Transepithelial electrical resistance (TEER) was measured using an epithelial voltohmmeter. Autophagy was determined by transmission electron microscopy (TEM), the ratio of LC3-II to LC3-I and the persistence of both green fluorescent protein (GFP) and mCherry signals using a tandem mCherry-GFP-LC3 construct. The expression of Atg12-Atg5-Atg16 complex was measured by quantitative real-time polymerase chain reaction.
EPEC-LPS significantly diminished the TEER of IEC compared with untreated controls by 45-55%. This reduction was not observed after treated with Bifidobacteria at all time points. Bifidobacteria could initiate the activation of autophagy in IEC, based on both the ratio of LC3-II to LC3-I and TEM. There was no difference in the influence of the four types of Bifidobacteria on the autophagy response. Compared with Bifidobacteria, IEC reacted to EPEC-LPS much more intensively by autophagy accumulation. More mCherry(+) LC3 autophagic puncta and increased expressions of autophagy genes Atg5, Atg12 and Atg16 could be detected after being treated with Bifidobacteria and EPEC-LPS.
Bifidobacteria initiate autophagy activation in IEC. The Atg12-Atg5-Atg16 multimeric complex might participate in the activation of Bifidobacteria-induced cell autophagy.
研究肠道微生物群对肠上皮细胞(IEC)自噬激活的影响,并评估IEC对不同类型双歧杆菌的自噬反应。
用源自肠致病性大肠杆菌(EPEC)O127:B8的脂多糖(LPS)和四种双歧杆菌的培养基上清液处理IEC-18细胞。使用上皮电压电阻计测量跨上皮电阻(TEER)。通过透射电子显微镜(TEM)、LC3-II与LC3-I的比值以及使用串联mCherry-GFP-LC3构建体检测绿色荧光蛋白(GFP)和mCherry信号的持续性来确定自噬。通过定量实时聚合酶链反应测量Atg12-Atg5-Atg16复合物的表达。
与未处理的对照相比,EPEC-LPS使IEC的TEER显著降低45%-55%。在所有时间点用双歧杆菌处理后均未观察到这种降低。基于LC3-II与LC3-I的比值和TEM,双歧杆菌可启动IEC中的自噬激活。四种双歧杆菌对自噬反应的影响没有差异。与双歧杆菌相比,IEC对EPEC-LPS的自噬积累反应更强烈。用双歧杆菌和EPEC-LPS处理后,可以检测到更多的mCherry(+) LC3自噬斑点以及自噬基因Atg5、Atg12和Atg16的表达增加。
双歧杆菌启动IEC中的自噬激活。Atg12-Atg5-Atg16多聚体复合物可能参与双歧杆菌诱导的细胞自噬激活。