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高迁移率族蛋白B1在脂多糖诱导的Caco-2细胞上皮屏障损伤中的作用
引用本文:陈晓雷,陈思如,修光辉,陈献忠,孙洁,凌斌,刘萍. 高迁移率族蛋白B1在脂多糖诱导的Caco-2细胞上皮屏障损伤中的作用[J]. 中华急诊医学杂志, 2021, 30(3): 287-292. DOI: 10.3760/cma.j.issn.1671-0282.2021.03.006
作者姓名:陈晓雷  陈思如  修光辉  陈献忠  孙洁  凌斌  刘萍
作者单位:云南大学附属医院(云南省第二人民医院)重症医学科, 昆明 650021
基金项目:国家自然科学基金(81901950);云南省科技厅-昆明医科大学联合专项基金[2017FE467(-194),2018FE001(-078),2019FE001(-009),202001AY070001-166];云南省基础研究计划项目(2019FB099);云南省高层次卫生计生技术人才培养经费资助(H-2017060);徐俊专家工作站(2017IC025)
摘    要:目的:探讨高迁移率族蛋白B1(high mobility group box 1,HMGB1)在脂多糖(lipopolysaccharide,LPS)诱导的Caco-2细胞肠上皮屏障损伤中的作用及机制。方法:用Transwell小室培养Caco-2细胞,检测跨上皮电阻值(TEER值),当TEER值达到500 Ω·cm...

关 键 词:脓毒症  肠上皮屏障功能  高迁移率族蛋白B1  脂多糖  Caco-2细胞

The role of high mobility group box 1 in the injury of Caco-2 epithelial barrier induced by lipopolysaccharide
Chen Xiaolei,Chen Siru,Xiu Guanghui,Chen Xianzhong,Sun Jie,Ling Bin,Liu Ping. The role of high mobility group box 1 in the injury of Caco-2 epithelial barrier induced by lipopolysaccharide[J]. Chinese Journal of Emergency Medicine, 2021, 30(3): 287-292. DOI: 10.3760/cma.j.issn.1671-0282.2021.03.006
Authors:Chen Xiaolei  Chen Siru  Xiu Guanghui  Chen Xianzhong  Sun Jie  Ling Bin  Liu Ping
Affiliation:(Department of Critical Care Medicine,the Affiliated Hospital of Yunnan University(the Second People's Hospital of Yunnan Province),Kunming 650021,China)
Abstract:Objective:To investigate the role and mechanism of high mobility group box 1(HMGB1) in the injury of Caco-2 intestinal epithelial barrier induced by lipopolysaccharide (LPS).Methods:The Caco-2 cellular monolayer barrier was established with Transwell chamber. After the Caco-2 monolayer model was established, the transepithelial electrical resistance (TEER) values were measured. When the TEER value reached 500 Ω·cm 2, the cells were divided into 3 groups: control group, LPS treatment group, and LPS+ ethyl pyruvate (EP) treatment group. The concentration of LPS and EP were 100 μg/mL, 50 μg/mL, separately. Then TEER values were measured at 12, 24, 48 and 72 h, and FITC-dextran permeability was detected at 24 h. The cells were seeded on 6-well plates. After cell density reached 80%, treatments were given as the above. The real-time polymerase chain reaction (RT-PCR) and Western blot were used to measure the changes in the protein and mRNA expressions of Occludin, HMGB1, and nuclear factor-κB (NF-κB). Results:Compared with the control group, the TEER values (Ω·cm 2) reduced at 12, 24, 48 and 72 h in the LPS treatment group [(514.22±12.59) vs (304.96±9.69), (521.65±13.35) vs (276.21±7.82), (523.99±8.18) vs (206.64±15.85), (491.21±6.72) vs (156.33±10.83), all P<0.05]. The FITC-dextran permeability increased significantly at 24 h [(2.58±0.07) vs (1.04±0.06), P<0.05]. The expression levels of Occludin protein and mRNA were decreased (all P<0.05), while the expression levels of HMGB1 and NF-κB protein and mRNA were significantly increased (all P<0.05). Compared with the LPS treatment group, the TEER values (Ω·cm 2) increased significantly at 12, 24, 48 and 72 h in the EP treatment group [(519.00±5.66) vs (304.96±9.69), (504.69±8.57) vs (276.21±7.82), (453.65±10.74) vs (206.64±15.85), (385.28±7.57) vs (156.33±10.83), all P<0.05]. The FITC-dextran permeability decreased at 24 h [(1.23±0.11) vs (2.58±0.07), P<0.05]. The expression level of Occludin protein and mRNA were increased ( P<0.05), while the expression levels of HMGB1 and NF-κB protein and mRNA were significantly decreased (all P<0.05). Conclusions:LPS can injure intestinal barrier directly in vitro and reduces the expression of tight junction proteins between cells. The mechanism may be related to the increased expression of HMGB1 and NF-κB protein.
Keywords:Sepsis  Intestinal epithelial barrier function  High mobility group box 1  Lipopolysaccharide  Caco-2 cells
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