[1]张丽君,袁俊婕,赵经文,等.Akkermansia muciniphila上清通过抑制内质网应激改善小肠黏膜损伤[J].天津医科大学学报,2024,30(06):528-534.[doi:10.20135/j.issn.1006-8147.2024.06.0528]
ZHANG Lijun,YUAN Junjie,ZHAO Jingwen,et al.Akkermansia muciniphila supernatant improves intestinal mucosal injury by inhibiting endoplasmic
reticulum stress[J].Journal of Tianjin Medical University,2024,30(06):528-534.[doi:10.20135/j.issn.1006-8147.2024.06.0528]
点击复制
Akkermansia muciniphila上清通过抑制内质网应激改善小肠黏膜损伤(PDF)
《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]
- 卷:
-
30卷
- 期数:
-
2024年06期
- 页码:
-
528-534
- 栏目:
-
基础医学
- 出版日期:
-
2024-11-20
文章信息/Info
- Title:
-
Akkermansia muciniphila supernatant improves intestinal mucosal injury by inhibiting endoplasmic
reticulum stress
- 文章编号:
-
1006-8147(2024)06-0528-07
- 作者:
-
张丽君1; 袁俊婕1; 赵经文1; 2; 陈鑫1; 2
-
(1.天津医科大学总医院消化科,天津300052;2.天津市消化疾病研究所,天津市消化病学重点实验室,天津300052)
- Author(s):
-
ZHANG Lijun1; YUAN Junjie1; ZHAO Jingwen1; 2; CHEN Xin1; 2
-
(1.Department of Gastroenterology and Hepatology,General Hospital,Tianjin Medical University,Tianjin 300052,China;2.Tianjin Institute of Digestive Diseases,Tianjin Key Laboratory of Digestive Diseases,Tianjin 300052,China)
-
- 关键词:
-
AKK上清; 内质网应激; NSAIDs; 小肠黏膜损伤
- Keywords:
-
AKK supernatant; endoplasmic reticulum stress; NSAIDs; intestinal mucosal injury
- 分类号:
-
R574.5
- DOI:
-
10.20135/j.issn.1006-8147.2024.06.0528
- 文献标志码:
-
A
- 摘要:
-
目的:探究Akkermansia muciniphila(AKK)上清对非甾体类抗炎药(NSAIDs)导致小肠黏膜损伤的干预效果及作用机制。方法:将18只C57BL/6小鼠(6~8周龄)采用随机数字表法随机分为3组:正常对照组(CON组)、造模组(INDO组)、干预组(INDO+AKK组),每组6只。INDO组使用吲哚美辛构建NSAIDs小肠损伤模型,INDO+AKK组使用AKK上清灌胃。采集各组肠道标本,常规苏木精-伊红(HE)染色观察黏膜屏障形态,免疫组织化学染色法(IHC)观察黏膜屏障指标咬合蛋白(Occuldin)、闭锁小带蛋白(ZO1)、黏蛋白2(MUC2)的表达水平。采用实时荧光定量PCR(qRT-PCR)从mRNA水平验证MUC2、葡萄糖调节蛋白78(GRP78)、X盒结合蛋白1(XBP1s)、C/EBP坏死因子相关蛋白(CHOP)、激活转录因子4(ATF4)、激活转录因子6(ATF6)、真核翻译起始因子2α激酶3(PERK)等基因的表达变化。结果:小肠组织HE染色观察发现,与CON组相比,INDO组出现小肠黏膜结构破坏、绒毛明显减少等特征。INDO+AKK组小肠黏膜损伤减轻、绒毛丧失现象减少、黏膜及其下层的炎症细胞浸润区域也显著减小。IHC分析显示,与INDO组相比,INDO+AKK组Occuldin(F=11.48,P<0.05)、ZO1(F=68.10,P<0.001)、MUC2(F=19.93,P<0.01)表达水平增加。PAS结果显示,INDO+AKK组杯状细胞数量相对于INDO组明显增加(F=205.9,P<0.001)。qRT-PCR结果发现,与INDO组相比,INDO+AKK组MUC2的基因(F=23.67,P<0.01)表达水平升高,GRP78(F=7.869,P<0.01)、CHOP(F=11.45,P<0.05)、XBP1s(F=8.344,P<0.05)、ATF4(F=16.37,P<0.001)、ATF6(F=12.99,P<0.001)、PERK(F=11.58,P<0.01)的基因表达水平均下降。结论:AKK上清通过抑制内质网应激,改善NSAIDs诱导的小肠黏膜屏障损伤。
- Abstract:
-
Objective: To investigate the effect and mechanism of Akkermansia muciniphila (AKK) supernatant on intestinal mucosal injury induced by non-steroidal anti-inflammatory drugs (NSAIDs). Methods:Eighteen C57BL/6 mice (6-8 weeks of age) were randomly divided into three groups by random number table method: normal control group (CON),modeling group (INDO) and intervention group (INDO+AKK),with 6 mice in each group. INDO group was treated with Indomethacin to establish the small intestine injury model of NSAIDs,INDO+AKK group was treated with AKK supernatant by oral gavage. Intestinal samples of each group were collected,and mucosal barrier morphology was observed by hematoxylin-eosin (HE) staining,mucosal barrier indexes occuldin,zona occlusa (ZO1),and mucin 2 (MUC2) were observed by immunohistochemical staining (IHC),and goblet cell number was observed by periodic Schiff (PAS) staining. Real-time quantitative fluorescent PCR (qRT-PCR) was used to verify the expression changes of MUC2,glucose regulatory protein 78 (GRP78),X-box binding protein 1 (XBP1s),C/EBP necrosis factor related protein (CHOP),activated transcription factor 4 (ATF4),activated transcription factor 6 (ATF6),and eukaryotic translation initiation factor 2α kinase 3 (PERK). and other genes at mRNA level. Results:HE staining of small intestine tissue revealed that compared with CON group,INDO group showed damage of intestinal mucosal structure and reduced villi. In the INDO+AKK group,the damage of small intestinal mucosa and the loss of villi were reduced,and the areas infiltrated by inflammatory cells in the mucosa and its sublayer were also significantly reduced. IHC analysis showed that Occuldin (F=11.48,P<0.05),ZO1(F=68.10,P<0.001) and MUC2 (F=19.93,P<0.01) expression levels were increased in INDO+AKK group compared with INDO group. PAS results showed that the number of goblet cells in INDO+AKK group was significantly increased compared with INDO group (F=205.9,P<0.001). The results of qRT-PCR showed that compared with the INDO group,the expression level of MUC2 gene (F= 23.67,P<0.01) was increased in the INDO+AKK group,GRP78 (F=7.869,P<0.01),CHOP (F=11.45,P<0.05),XBP1s (F=8.344,P<0.05),ATF4 (F=16.37,P<0.001),ATF6(F=12.99,P<0.001),PERK (F=11.58,P<0.01) were all decreased. Conclusion:AKK supernatant can ameliorate NSAIDs induced intestinal mucosal barrier injury by inhibiting ER stress.
参考文献/References:
[1] LANAS A,GARC?魱A-RODR?魱GUEZ L A,POLO-TOM?魣S M,et al. Time trends and impact of upper and lower gastrointestinal bleeding and perforation in clinical practice[J]. Am J Gastroenterol,2009, 104(7):1633-1641.
[2] TAI F,MCALINDON M E. Non-steroidal anti-inflammatory drugs and the gastrointestinal tract[J]. Clin Med (Lond),2021,21(2):131-134.
[3] GRAHAM D Y,OPEKUN A R,WILLINGHAM F F,et al. Visible small-intestinal mucosal injury in chronic NSAID users[J]. Clin Gastroenterol Hepatol,2005,3(1):55-59.
[4] CANI P D,DEPOMMIER C,DERRIEN M,et al. Akkermansia muciniphila: paradigm for next-generation beneficial microorganisms[J]. Nat Rev Gastroenterol Hepatol,2022,19(10):625-637.
[5] PEREZ-VILAR J,HILL R L. The structure and assembly of secreted mucins[J]. J Biol Chem,1999,274(45):31751-31754.
[6] 聂烁,闻正顺. 肠道黏蛋白2的分泌、结构、合成调控及其在肠道疾病发生发展中的作用[J]. 动物营养学报,2020,32(6):2521-2532.
[7] BOELSTERLI U A,REDINBO M R,SAITTA K S. Multiple NSAID-induced hits injure the small intestine: underlying mechanisms and novel strategies[J]. Toxicol Sci,2013,131(2):654-667.
[8] LICHTENBERGER L M,ZHOU Y,JAYARAMAN V,et al. Insight into NSAID-induced membrane alterations,pathogenesis and therapeutics: characterization of interaction of NSAIDs with phosphatidylcholine[J]. Biochim Biophys Acta,2012,1821(7):994-1002.
[9] SANDOVAL-ACU?譙A C,LOPEZ-ALARC?譫N C,ALIAGA M E,et al. Inhibition of mitochondrial complex I by various non-steroidal anti-inflammatory drugs and its protection by quercetin via a coenzyme Q-like action[J]. Chem Biol Interact,2012,199(1):18-28.
[10] SOMASUNDARAM S,SIGTHORSSON G,SIMPSON R J,et al. Uncoupling of intestinal mitochondrial oxidative phosphorylation and inhibition of cyclooxygenase are required for the development of NSAID-enteropathy in the rat[J]. Aliment Pharmacol Ther,2000,14(5):639-650.
[11] LOGUIDICE A,RAMIREZ-ALCANTARA V,PROLI A,et al. Pharmacologic targeting or genetic deletion of mitochondrial cyclophilin D protects from NSAID-induced small intestinal ulceration in mice[J]. Toxicol Sci,2010,118(1):276-285.
[12] LOGUIDICE A,WALLACE B D,BENDEL L,et al. Pharmacologic targeting of bacterial β-glucuronidase alleviates nonsteroidal anti-inflammatory drug-induced enteropathy in mice[J]. J Pharmacol Exp Ther,2012,341(2):447-454.
[13] HARUSATO A,NAITO Y,TAKAGI T,et al. Suppression of indomethacin-induced apoptosis in the small intestine due to Bach1 deficiency[J]. Free Radic Res,2011,45(6):717-727.
[14] OHYAMA K,SHIOKAWA A,ITO K,et al. Toxicoproteomic analysis of a mouse model of nonsteroidal anti-inflammatory drug-induced gastric ulcers[J]. Biochem Biophys Res Commun,2012,420(1):210-215.
[15] WATANABE T,HIGUCHI K,KOBATA A,et al. Non-steroidal anti-inflammatory drug-induced small intestinal damage is Toll-like receptor 4 dependent[J]. Gut,2008,57(2):181-187.
[16] NADATANI Y,WATANABE T,TANIGAWA T,et al. High mobility group box 1 promotes small intestinal damage induced by nonsteroidal anti-inflammatory drugs through Toll-like receptor 4[J]. Am J Pathol,2012,181(1):98-110.
[17] FUKUMOTO K,NAITO Y,TAKAGI T,et al. Role of tumor necrosis factor-α in the pathogenesis of indomethacin-induced small intestinal injury in mice[J]. Int J Mol Med,2011,27(3):353-359.
[18] REUTER B K,DAVIES N M,WALLACE J L. Nonsteroidal anti-inflammatory drug enteropathy in rats: role of permeability,bacteria,and enterohepatic circulation[J]. Gastroenterology,1997,112(1):109-117.
[19] 易俊,刘小伟. 炎症性肠病的肠道屏障功能研究进展[J]. 中华炎性肠病杂志,2019,3(1):41-44.
[20] HEAZLEWOOD C K,COOK M C,ERI R,et al. Aberrant mucin assembly in mice causes endoplasmic reticulum stress and spontaneous inflammation resembling ulcerative colitis[J]. PLoS Med,2008,5(3):e54.
[21] NAAMA M,TELPAZ S,AWAD A,et al. Autophagy controls mucus secretion from intestinal goblet cells by alleviating ER stress[J]. Cell Host Microbe,2023,31(3):433-446,e4.
相似文献/References:
[1]江天铎,程欣欣,徐哲龙.锌转运体ZIP13在小鼠肝脏缺血再灌注损伤中的作用[J].天津医科大学学报,2022,28(05):459.
JIANG Tian-duo,CHENG Xin-xin,XU Zhe-long.Role of zinc transporter ZIP13 in hepatic ischemia/reperfusion injury in mice[J].Journal of Tianjin Medical University,2022,28(06):459.
备注/Memo
- 备注/Memo:
-
基金项目 天津市卫生健康科技项目(TJWJ2021MS005)
作者简介 张丽君(1997-),女,硕士,研究方向:上消化道疾病小肠损伤;
通信作者:陈鑫,E-mail:xchen03@tmu.edu.cn。
更新日期/Last Update:
2024-11-25