肠道菌群、GRP78、TLR4在大鼠肝硬化发生发展中的作用#br#

doi:10.13418/j.issn.1001-165x.2019.03.004

中国临床解剖学杂志 ›› 2019, Vol. 37 ›› Issue (3): 254-260.doi: 10.13418/j.issn.1001-165x.2019.03.004

肠道菌群、GRP78、TLR4在大鼠肝硬化发生发展中的作用#br#

陈云霞¹，　张慧英²，　杨泽溪³，　来丽娜⁴，　孟莉¹，　李旭炯⁵

长治医学院　1.微生物学教研室, 2.病理生理学教研室, 3.基础医学部, 4.药理学教研室, 5.生理学教研室，山西长治 046000

收稿日期:2018-12-29 出版日期:2019-05-25 发布日期:2019-06-13
通讯作者: 张慧英，博士，教授，E-mail：zhanghy2001@163.com
作者简介:陈云霞(1972-)，山西晋城人，硕士，副教授，主要研究方向为肠道菌群与疾病，E-mail： chyxwyt@163.com
基金资助:
国家自然科学基金(81070339)；山西省自然科学基金(201601D011092)；山西省卫生计生委科研课题(2017156)；山西省高等学校大学生创新创业训练计划项目(2017313)；长治医学院创新团队资助经费项目(CX201508)；长治医学院普及项目(QDZ201631)

Effects of gut microbiota, GRP78 and TLR4 on the development of liver cirrhosis in rats

CHEN Yun-xia¹, ZHANG Hui-ying², YANG Ze-xi³, LAI Li-na⁴, MENG Li¹, LI Xu-jiong⁵

1.Department of Microbiology, 2.Department of Pathophysiology, 3. Department of Basic Medical, 4. Department of Pharmacology, 5.Department of Physiology, Changzhi Medical College, Changzhi 046000, Shaanxi Province, China

Received:2018-12-29 Online:2019-05-25 Published:2019-06-13

摘要/Abstract

摘要： 目的　探讨肠道菌群、肠组织中内质网应激蛋白GRP78（glucose-regulated protein 78）、模式识别受体TLR4（toll-like receptors 4）表达水平的改变在大鼠肝硬化发生发展中的作用。方法　采用复合致病因素法诱导大鼠肝硬化。HE染色观察肝与小肠病理学改变，ARISA（automated ribosomal intergenic-spacer analysis）分析回肠内容物肠道菌群组成，培养法检测各组动物细菌易位情况，ELISA（enzyme-linked immunosorbent assay）测定血浆生化指标，quantitative real-time PCR、Western blotting检测肝、肠组织GRP78、TLR4的表达。结果　肝硬化模型动物肝、肠组织病理学改变明显。随着肝硬化的进展，模型动物血浆中ALT（alanine aminotransferase）、内毒素和Hcy（homocysteine）的水平逐渐增高。模型组与对照组间肠道菌群的组间相似性明显降低。模型组发生细菌易位的大鼠数量、易位率显著升高。模型组动物肝、肠组织中GRP78的表达水平均随病程进展显著升高；肝组织中TLR4的表达水平在6周之前随病程进展显著升高，8周仍明显高于正常动物，但低于6周时的表达水平；肠组织中TLR4的表达水平在6周之前随病程进展显著升高，8周则明显降低。结论　肠道微生物群落结构的生态失调、应激水平升高、免疫功能下降，导致肠道细菌易位，加重肝损伤，促进肝硬化形成。

关键词: 肝硬化, 　肠道菌群, 　细菌易位, 　GRP78, 　TLR4

Abstract: Objective 　To study the effects of gut microbiota, glucose-regulated protein 78 (GRP78) and toll-like receptors 4 (TLR4) on the development of liver cirrhosis in rats.　Methods　Thirty-six male SD rats were randomly divided into a normal control group (N) and a hepatic cirrhosis model group (M). The liver cirrhosis was induced by compound factors. Each group was sampled at 4, 6 and 8 week time points. Injuries of liver and intestinal mucosa were assessed with H&E stain. The gut microbiota was examined with automated ribosomal intergenic-spacer analysis (ARISA) on fecal DNA, and the bacterial translocation was assessed by standard microbiological techniques on blood, mesenteric lymph nodes (MLN), ascites and liver. The levels of alanine aminotransferase (ALT), endotoxin and homocysteine (Hcy) in the plasma were detected by enzyme-linked immunosorbent assay (ELISA). The expression of GRP78 and TLR4 was analyzed using quantitative real-time PCR and Western blotting.　Results　Compared to group N, the pathologic change of liver and small intestine was obvious in group M, and the levels of ALT, endotoxin, Hcy in the plasma were significantly and gradually increased. The occurrence of bacterial translocation (BT) was increased in the liver of group M compared to that of group N. BT was not detected in the blood in any group. The expression of GRP78 was significantly and gradually increased in the tissues of liver and ileum in group M. In liver homogenate, the expression of TLR4 in group M was significantly and gradually increased in 6 weeks, and significantly higher than group N at 8 weeks, but lower than group M at 6 weeks. In ileal homogenate, the expression of TLR4 in group M was also significantly and gradually increased in 6 weeks, but was significantly decreased than group N at 8 weeks.　Conclusion　With the progress of liver cirrhosis, the dysbiosis of gut microbiota becomes more and more serious, the expression of GRP78 increases significantly and the expression level of TLR4 decreases significantly in ileal homogenate, which may result in the gradual increase of the intestinal mucosal barrier damage, and cause significant increase of the occurrence of BT and level of endotoxin, eventually affecting the expression of GRP78 and TLR4 in liver, and worsening liver injury then.

Key words: Hepatic cirrhosis, 　Gut microbiota, 　Bacterial translocation, 　GRP78, 　TLR4

中图分类号:

R363.1

陈云霞, 张慧英, 杨泽溪, 来丽娜, 孟莉, 李旭炯. 肠道菌群、GRP78、TLR4在大鼠肝硬化发生发展中的作用#br#[J]. 中国临床解剖学杂志, 2019, 37(3): 254-260.

CHEN Yun-xia, ZHANG Hui-ying, YANG Ze-xi, LAI Li-na, MENG Li, LI Xu-jiong . Effects of gut microbiota, GRP78 and TLR4 on the development of liver cirrhosis in rats[J]. Chinese Journal of Clinical Anatomy, 2019, 37(3): 254-260.

参考文献 30

[1]	Tilg H, Cani PD, Mayer EA. Gut microbiome and liver diseases[J]. Gut, 2016, 65(12): 2035-2044.
[2]	Chen LW, Chang WJ, Chen PH, et al. Commensal microflora induce host defense and decrease bacterial translocation in burn mice through toll-likereceptor 4[J]. J Biomed Sci, 2010, 17: 48-62.
[3]	Izcue A, Coombes JL, Powrie F. Regulatory lymphocytes and intestinal inflammation[J]. Annu Rev Immunol, 2009, 27: 313-338.
[4]	MacDonald TT, Monteleone I, Fantini MC, et al. Regulation of homeostasis and inflammation in the intestine[J]. Gastroenterology, 2011, 140(6): 1768-1775.
[5]	Lawrance IC. Microbiota and management of inflammatory bowel disease[J]. J Gastroenterol Hepatol, 2012, 27(7): 1137-1140.
[6]	Fujimoto T, Imaeda H, Takahashi K, et al. Decreased abundance of Faecalibacterium prausnitzii in the gut microbiota of Crohn's disease[J]. J Gastroenterol Hepatol, 2013, 28(4): 613-619.
[7]	Arvaniti V, D'Amico G, Fede G, et al. Infections in patients with cirrhosis increase mortality four-fold and should be used in determining prognosis[J]. Gastroenterology, 2010, 139(4): 1246-1256, 1256.e1–5.
[8]	McLaughlin D, Shellenback L. Sepsis in patients with cirrhosis[J]. AACN Adv Crit Care, 2016, 27(4): 408-419.
[9]	Seki E, De Minicis S, Osterreicher CH, et al. TLR4 enhances TGF-beta signaling and hepatic fibrosis[J]. Nat Med, 2007, 13(11): 1324-1332.
[10]	Zhang HY, Han DW, Zhao ZF, et al. Multiple pathogenic factor-induced complication of cirrhosis in rats: a new model of hepatopulmonary syndrome with intestinal endotoxemia[J]. World J Gastroenterol, 2007, 13(25): 3500-3507.
[11]	陈云霞, 张慧英, 孟莉, 等. 肝硬化大鼠细菌易位以及甜菜碱的干预作用[J]. 微生物学通报, 2014, 41(8):1629-1636.
[12]	Chen YX, Lai LN, Zhang HY, et al. Effect of artesunate supplementation on bacterial translocation and dysbiosis of gut microbiota in rats with liver cirrhosis[J]. World J Gastroenterol, 2016, 22(10): 2949-2959.
[13]	Cardinale M, Brusetti L, Quatrini P, et al. Comparison of different primer sets for use in automated ribosomal intergenic spacer analysis of complex bacterial communities[J]. Appl Environ Microbio, 2004, 70(10): 6147-6156.
[14]	Wiest R, Albillos A, Trauner M, et al. Targeting the gut-liver axis in liver disease[J]. J Hepatol, 2017, 67(5): 1084-1103.
[15]	Frasinariu OE, Ceccarelli S, Alisi A, et al. Gut-liver axis and fibrosis in nonalcoholic fatty liver disease: an input for novel therapies[J]. Dig Liver Dis, 2013, 45(7): 543-551.
[16]	Qin N, Yang F, Li A, et al. Alterations of the human gut microbiome in liver cirrhosis[J]. Nature, 2014, 513(7516): 59-64.
[17]	Vanhoutvin SA, Troost FJ, Hamer HM, et al. Butyrate-induced transcriptional changes in human colonic mucosa[J]. PLoS ONE, 2009, 4(8): e6759-6764.
[18]	Peng L, Li ZR, Green RS, et al. Butyrate enhances the intestinal barrier by facilitating tight junction assembly via activation of AMP-activated protein kinase in Caco-2 cell monolayers[J]. J Nutr, 2009, 139(9): 1619-1625.
[19]	Segain JP, Raingeard de la Blétière D, Bourreille A, et al. Butyrate inhibits inflammatory responses through NFkappaB inhibition: implications for Crohn’s disease[J]. Gut, 2000, 47(3): 397-403.
[20]	Lührs H, Gerke T, Schauber J, et al. Cytokine-activated degradation of inhibitory kappaB protein alpha is inhibited by the short chain fatty acid butyrate[J]. Int J Colorectal Dis, 2001, 16(4): 195-201.
[21]	Henao-Mejia J, Elinav E, Jin C, et al. Inflammasome-mediated dysbiosis regulates progression of NAFLD and obesity[J]. Nature, 2012, 482(7384): 179-185.
[22]	Gjymishka A, Coman RM, Brusko TM, et al. Influence of host immunoregulatory genes, ER stress and gut microbiota on the shared pathogenesis of inflammatory bowel disease and Type 1 diabetes[J]. Immunotherapy, 2013, 5(12): 1357-1366.
[23]	Görlach A, Klappa P, Kietzmann T. The endoplasmic reticulum: Folding, calcium homeostasis, signaling, and redox control[J]. Antioxid Redox Signal, 2006, 8(9-10): 1391-1418.
[24]	Ji C. Dissection of endoplasmic reticulum stress signaling in alcoholic and non-alcoholic liver injury[J]. J Gastroenterol Hepatol, 2008, 23 (Suppl 1): S16-S24.
[25]	Dupaul-Chicoine J, Yeretssian G, Doiron K, et al. Control of intestinal homeostasis, colitis, andcolitis-associated colorectal cancer by the inflammatory caspases[J]. Immunity, 2010, 32(3): 367-378.
[26]	Wu YY, Hsu CM, Chen PH, et al. Toll-like receptor stimulation induces nondefensin protein expression and reverses antibiotic-induced gut defense impairment[J]. Infect Immun, 2014, 82(5): 1994-2005.
[27]	Zhang HY, Han DW, Wang XG, et al. Experimental study on the role of endotoxin in the development of hepatopulmonary syndrome[J]. World J Gastroenterol, 2005, 11(4): 567-572.
[28]	Zhang HY, Han DW, Su AR, et al. Intestinal endotoxemia plays a central role in development of hepatopulmonary syndrome in a cirrhotic rat model induced by multiple pathogenic factors[J]. World J Gastroenterology, 2007, 13(47): 6385-6395.
[29]	Xiu F, Catapano M, Diao L, et al. Prolonged endoplasmic reticulum-stressed hepatocytes drive an alternative macrophage polarization[J]. Shock, 2015, 44(1): 44-51.
[30]	田小霞, 张慧英, 陈云霞, 等. 巨噬细胞极化在大鼠肝硬化发生发展中的作用[J]. 中国病理生理杂志, 2016, 32(5): 880-885.

肠道菌群、GRP78、TLR4在大鼠肝硬化发生发展中的作用#br#

Effects of gut microbiota, GRP78 and TLR4 on the development of liver cirrhosis in rats

可视化

摘要/Abstract

引用本文

使用本文

参考文献 30

相关文章 7

Metrics

本文评价

推荐阅读 0

[1]	李文豪, 齐宝宁, 施艺, 王昱昊, 赵再华, 王瑜, 沈学锋. 模拟高原低氧小鼠学习记忆能力与肠道菌群结构改变的相关性研究[J]. 中国临床解剖学杂志, 2023, 41(3): 296-303.
[2]	李斯锐, 吴宁, 黄渭, 卢先明, 马明昭. 肝硬化PHT经颈内静脉肝内门体分流术前后的肝CT类灌注成像研究[J]. 中国临床解剖学杂志, 2023, 41(2): 234-239.
[3]	臧成昊, 杨金伟, 马微, 梁宇, 刘矿嫔, 刘伟, 刘洁, 王国栋, 张丝嘉, 吴红杰, 朱科威, 郭建辉, 李力燕. 小肠缺血时间与GRP78表达的相关性研究及意义[J]. 中国临床解剖学杂志, 2022, 40(4): 418-424.
[4]	李琛, 张英杰, 孙洋, 王洪新. 视黄酸通过TLR4/NF-κB通路对脂多糖诱导血管炎症与氧化应激的影响[J]. 中国临床解剖学杂志, 2022, 40(3): 303-308.
[5]	王昱昊, 施艺, 李文豪, 王舒, 沈学锋, 杨建军. 肠道菌群在高原低氧肠道损伤中的作用研究[J]. 中国临床解剖学杂志, 2021, 39(6): 666-672.
[6]	胡辉莹, 胡银霞, 刘昌顺, 苏小婷, 戴辉. 润燥止痒胶囊对银屑病样皮损大鼠肠道菌群和炎症反应的影响[J]. 中国临床解剖学杂志, 2020, 38(5): 574-577.
[7]	王剑华, 周庭永, 张本斯, 成家茂, 李彦彦, 李林宏, 杜赵康. 64层螺旋CT在DIPS术模拟穿刺途径测量中的应用[J]. 中国临床解剖学杂志, 2011, 29(3): 304-307.