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细胞毒性T淋巴细胞的穿孔素和颗粒酶B介导细胞凋亡,与幽门螺杆菌感染无关:可能是消化性溃疡形成的触发因素。

Perforin and granzyme B of cytotoxic T lymphocyte mediate apoptosis irrespective of Helicobacter pylori infection: possible act as a trigger of peptic ulcer formation.

作者信息

Ohara Tadashi, Morishita Tetsuo, Suzuki Hidekazu, Masaoka Tatsuhiro, Ishii Hiromasa

机构信息

Department of Internal Medicine, Tokyo Dental College, Chiba Hospital, Ichikawa General Hospital, Chiba, Japan.

出版信息

Hepatogastroenterology. 2003 Nov-Dec;50(54):1774-9.

Abstract

BACKGROUND/AIMS: The perforin/granzyme and Fas/Fas ligand pathways are two known major pathways of cytotoxic T lymphocyte-mediated apoptosis. We designed a clinical study to examine whether cytotoxic T lymphocyte-mediated apoptosis associated with peptic ulcer formation may occur via either or both of these two pathways.

METHODOLOGY

Mucosal biopsy specimens were obtained endoscopically from the marginal zone of active stage gastric and duodenal ulcers in patients with or without Helicobacter pylori infection. RT-PCR, immunoblotting and immunohistochemistry were used to study the samples for the expression of apoptotic cells, perforin, granzyme B, Fas, Fas ligand and caspase 3.

RESULTS

Apoptotic cells (Tunnel positive cells) appeared in the marginal zone of gastric and duodenal ulcers with and without H. pylori infection. Perforin/granzyme B and caspase 3 were expressed consistently, however Fas ligand was not. Furthermore, the immunohistochemical findings demonstrated apoptotic changes of target cells caused by perforin/granzyme B.

CONCLUSIONS

These results suggest that the main pathway of cytotoxic T lymphocyte-mediated apoptosis in peptic ulcer formation is the perforin/granzyme pathway irrespective of H. pylori infection.

摘要

背景/目的:穿孔素/颗粒酶途径和Fas/Fas配体途径是细胞毒性T淋巴细胞介导的凋亡的两个已知主要途径。我们设计了一项临床研究,以检查与消化性溃疡形成相关的细胞毒性T淋巴细胞介导的凋亡是否可能通过这两个途径中的一个或两个发生。

方法

通过内镜从有或无幽门螺杆菌感染的胃和十二指肠溃疡活动期边缘区域获取黏膜活检标本。采用逆转录聚合酶链反应(RT-PCR)、免疫印迹和免疫组织化学方法研究样本中凋亡细胞、穿孔素、颗粒酶B、Fas、Fas配体和半胱天冬酶3的表达。

结果

在有和无幽门螺杆菌感染的胃和十二指肠溃疡边缘区域均出现凋亡细胞(TUNEL阳性细胞)。穿孔素/颗粒酶B和半胱天冬酶3持续表达,但Fas配体未表达。此外,免疫组织化学结果显示穿孔素/颗粒酶B导致靶细胞发生凋亡变化。

结论

这些结果表明,无论是否存在幽门螺杆菌感染,消化性溃疡形成过程中细胞毒性T淋巴细胞介导的凋亡的主要途径是穿孔素/颗粒酶途径。

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