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TNBS诱导结肠炎小鼠中细菌鞭毛蛋白的表达及其与肥大细胞脱颗粒的关系
引用本文:路瑶,郝卉杰,贺欣,张目涵,赵美华,马娜,冯百岁. TNBS诱导结肠炎小鼠中细菌鞭毛蛋白的表达及其与肥大细胞脱颗粒的关系[J]. 中国病理生理杂志, 2018, 34(6): 1081-1088. DOI: 10.3969/j.issn.1000-4718.2018.06.020
作者姓名:路瑶  郝卉杰  贺欣  张目涵  赵美华  马娜  冯百岁
作者单位:郑州大学第二附属医院消化内科, 炎症性肠病中心, 吴阶平医学基金会, 炎症性肠病联盟 河南省炎症性肠病中心, 河南 郑州 450014
基金项目:国家自然科学基金资助项目(No.81070288;No.81270452);河南省卫生计生科技创新型人才特聘学科带头人资助项目;河南省自然科学基金项目资助项目(No.162300410268);河南省医学科技攻关计划项目(No.201502015)
摘    要:
目的:研究不同炎症程度下2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎小鼠的血清及结肠组织中细菌鞭毛蛋白CBir1的表达、肥大细胞脱颗粒的情况及两者的相关性。方法:将SPF级雄性BALB/c小鼠随机分为6组,每组12只,分别是:正常对照组、生理盐水组、50%乙醇组、50%乙醇+TNBS组、50%乙醇+TNBS+酮替芬组及50%乙醇+TNBS+脂多糖(LPS)+卵清蛋白(OVA)组,同时对小鼠进行疾病活动指数(DAI)评分。分组处理后第22天处死并提取小鼠的血清及结肠组织,采用组织损伤指数(HI)评分标准对小鼠结肠进行组织病理评估,采用ELISA法检测抗-CBir1、组胺以及肥大细胞类胰蛋白酶(MCT)在小鼠血清中的浓度,并用免疫组化法检测小鼠结肠组织中CBir1、Toll样蛋白受体5(TLR5)及MCT的表达。结果:TNBS诱导组的DAI评分和HI评分,且CBir1、TLR5、MCT、抗-CBir1和组胺在肠黏膜和血清中的表达明显高于正常对照组(P0.05);50%乙醇+TNBS组上述数值除TLR5外均低于50%乙醇+TNBS+LPS+OVA组(P0.05);50%乙醇+TNBS组上述数值除MCT外则均高于50%乙醇+TNBS+酮替芬组(P0.05);生理盐水和50%乙醇组小鼠与正常对照组小鼠比较,上述数值差异无统计学显著性。将TNBS诱导模型组小鼠血清中抗-CBir1与MCT的浓度进行相关性分析,结果提示两者呈正相关(r=0.751,P0.01);此外,小鼠的血清中抗-CBir1与组胺的浓度亦呈正相关(r=0.648,P0.01)。结论:TNBS诱导结肠炎炎症程度越重的小鼠,其体内CBir1的表达量越高,同时肥大细胞脱颗粒作用也越明显。TNBS诱导结肠炎小鼠体内CBir1的表达量与肥大细胞脱颗粒作用呈正相关性。

关 键 词:2  4  6-三硝基苯磺酸  鞭毛蛋白  肥大细胞脱颗粒  炎症性肠病  
收稿时间:2017-09-18

Pathogenic effect of bacterial flagellin in TNBS-induced colitis in mice
LU Yao,HAO Hui-jie,HE Xin,ZHANG Mu-han,ZHAO Mei-hua,MA Na,FENG Bai-sui. Pathogenic effect of bacterial flagellin in TNBS-induced colitis in mice[J]. Chinese Journal of Pathophysiology, 2018, 34(6): 1081-1088. DOI: 10.3969/j.issn.1000-4718.2018.06.020
Authors:LU Yao  HAO Hui-jie  HE Xin  ZHANG Mu-han  ZHAO Mei-hua  MA Na  FENG Bai-sui
Affiliation:Department of Gastroenterology, The Second Affiliated Hospital of Zhengzhou University, Inflammatory Bowel Disease Center, Wu Jie-ping Medical Foundation, China Inflammatory Bowel Disease Coalition, Henan Inflammatory Bowel Disease Center, Zhengzhou 450014, China
Abstract:
AIM: To detect the expression of CBir1 in the serum and colon tissue and mast cell degranulation in the tissue of 2,4,6-trinito-benzene-sulfonic acid (TNBS)-induced colitis in mice with different interventions. ME-THODS: SPF male BALB/c mice were randomized into 6 groups (12 mice in each group):normal control group, normal saline group, 50% alcohol group, 50% alcohol+TNBS group, 50% alcohol+TNBS+lipopolysaccharide (LPS)+ovalbumin (OVA) group and 50% alcohol+TNBS+ketotifen group. Corresponding treatment was given to each group, and the disease activity index (DAI) of the mice was evaluated. The mice were sacrificed on day 22 after treatment. The colon tissues were evaluated by histological index (HI) scoring. Serum concentrations of anti-CBir1, mast cell tryptase (MCT) and histamine were measured by ELISA. The expression of CBir1, toll-like receptor 5 (TLR5) and MCT in the colon tissues was detected by immunohistochemistry. RESULTS: Compared with the normal control group, the DAI score, HI score and CBir1, anti-CBir1, MCT, TLR5, histamine concentrations in colon tissues and serum were all significantly higher in 50% alcohol+TNBS group, 50% alcohol+TNBS+ketotifen group and 50% alcohol+TNBS+LPS+OVA group (P<0.05). The DAI score, HI score and anti-CBir1, CBir1, MCT, histamine levels in 50% alcohol+TNBS group were lower than those in 50% alcohol+TNBS+LPS+OVA group (P<0.05). The DAI score, HI score and anti-CBir1, TLR5, histamine, CBir1 Levels in 50% alcohol+TNBS group were higher than those in 50% alcohol+TNBS+ketotifen group (P<0.05). Normal saline group and 50% alcohol group had no statistically significant difference in comparison with normal control group. In TNBS model group, serum concentration of anti-CBir1 was positively correlated with MCT concentration (r=0.648, P<0.01) and histamine concentration (r=0.751, P<0.01). CONCLUSION: The heavier degree of inflammation in TNBS-induced colitis, the higher levels of the CBir1 and the degranulation of mast cells. There is a positive correlation between the expression of CBir1 and the degranulation of mast cells in TNBS-induced colitic mice.
Keywords:2  4  6-Trinito-benzene-sulfonic acid  Flagellin  Mast cell degranulation  Inflammatory bowel disease
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