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人类和鼠类幽门螺杆菌感染中胃体部金属蛋白酶组织抑制剂表达的改变

Altered gastric corpus expression of tissue inhibitors of metalloproteinases in human and murine Helicobacter infection.

作者信息

Bodger K, Ahmed S, Pazmany L, Pritchard D M, Micheal A, Khan A L, Dimaline R, Dockray G J, Varro A

机构信息

Aintree Centre for Gastroenterology, University Hospital Aintree, Liverpool, UK.

出版信息

J Clin Pathol. 2008 Jan;61(1):72-8. doi: 10.1136/jcp.2007.048058. Epub 2007 Apr 5.

Abstract

BACKGROUND

Matrix metalloproteinases (MMPs) have roles in inflammation and other processes relevant to the architectural disturbances seen in the gastric mucosa in response to Helicobacter pylori infection. Upregulation of MMPs has been reported in H pylori infection, but there are no detailed reports regarding altered production of their inhibitors, the tissue inhibitors of metalloproteinases (TIMPs).

AIMS

To investigate changes in the abundance of TIMPs in human gastric corpus mucosa and murine stomach in Helicobacter infection, and to study cellular sources in man.

METHODS

Gastric corpus biopsy samples were assessed for abundance of mRNA or protein for TIMP-1 to -4 by real-time quantitative PCR or western blotting, respectively. Antral and corpus biopsies were processed for histology, H pylori status and inflammatory scoring. Cellular sources of TIMP-1, -3 and -4 were examined by indirect immunohistochemistry. Circulating gastrin was measured by radioimmunoassay. Also, abundance of TIMP-1, -3 and -4 mRNA in the stomach of Helicobacter felis infected mice post-infection was compared with that of uninfected control animals.

RESULTS

Compared with uninfected patients, mRNA and protein for TIMP-1, -3 and -4 were significantly more abundant in the gastric corpus of H pylori infected subjects. Gastric TIMP expression did not differ significantly between hyper- and normogastrinaemic subjects within the H pylori negative and positive groups. There was no difference in mRNA abundance for MMP-3 or -8. Immunohistochemistry showed TIMP proteins localised to gastric epithelial, stromal cells and inflammatory cells. Murine H felis infection was associated with upregulation of TIMP-1 and -3 mRNA.

CONCLUSIONS

Helicobacter infection is associated with upregulation of specific TIMPs (TIMP-1 and -3) in glandular epithelium and stroma. It is suggested that increased expression of specific protease inhibitors in the corpus mucosa may exert important effects on extracellular matrix remodelling and influence the outcome of H pylori infection.

摘要

背景

基质金属蛋白酶(MMPs)在炎症及其他与幽门螺杆菌感染后胃黏膜结构紊乱相关的过程中发挥作用。已有报道称幽门螺杆菌感染时MMPs上调,但关于其抑制剂金属蛋白酶组织抑制剂(TIMPs)产生变化的详细报道却未见。

目的

研究幽门螺杆菌感染时人胃体黏膜和鼠胃中TIMPs丰度的变化,并探究人体中的细胞来源。

方法

分别通过实时定量PCR或蛋白质印迹法评估胃体活检样本中TIMP-1至-4的mRNA或蛋白质丰度。对胃窦和胃体活检样本进行组织学、幽门螺杆菌状态及炎症评分处理。通过间接免疫组织化学检查TIMP-1、-3和-4的细胞来源。采用放射免疫分析法测定循环胃泌素。此外,将感染猫幽门螺杆菌的小鼠感染后胃中TIMP-1、-3和-4 mRNA的丰度与未感染的对照动物进行比较。

结果

与未感染患者相比,幽门螺杆菌感染受试者胃体中TIMP-1、-3和-4的mRNA和蛋白质明显更为丰富。在幽门螺杆菌阴性和阳性组中,高胃泌素血症和正常胃泌素血症受试者之间的胃TIMP表达无显著差异。MMP-3或-8的mRNA丰度无差异。免疫组织化学显示TIMP蛋白定位于胃上皮细胞、基质细胞和炎症细胞。鼠感染猫幽门螺杆菌与TIMP-1和-3 mRNA上调有关。

结论

幽门螺杆菌感染与腺上皮和基质中特定TIMPs(TIMP-1和-3)的上调有关。提示胃体黏膜中特定蛋白酶抑制剂表达增加可能对细胞外基质重塑产生重要影响,并影响幽门螺杆菌感染的结局。

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