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肿瘤坏死因子相关凋亡诱导配体及其受体在病毒性肝病中的作用

Involvement of tumor necrosis factor-related apoptosis-inducing ligand and tumor necrosis factor-related apoptosis-inducing ligand receptors in viral hepatic diseases.

作者信息

Saitou Yukiko, Shiraki Katsuya, Fuke Hiroyuki, Inoue Tomoko, Miyashita Kazumi, Yamanaka Yutaka, Yamaguchi Yumi, Yamamoto Norihik, Ito Keiichi, Sugimoto Kazushi, Nakano Takeshi

机构信息

First Department of Internal Medicine, Mie University School of Medicine, Tsu, Mie 514-8507, Japan.

出版信息

Hum Pathol. 2005 Oct;36(10):1066-73. doi: 10.1016/j.humpath.2005.07.019.

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induces apoptosis in tumor cells, but not in most normal cells. The role of TRAIL in hepatic cell death and hepatic diseases is not well understood. The present study investigated the expression of TRAIL and TRAIL receptors (TRAIL-Rs) in patients with hepatitis C virus infection using immunohistochemistry and examined physiological roles under viral infection in the HepG2 cell line. Staining of TRAIL or TRAIL-Rs was prominent in the cytoplasm and membrane of hepatocytes in the periportal area. Some liver-infiltrating lymphocytes also displayed positive staining for TRAIL. Staining intensity was significantly increased with disease progression, particularly in the periportal area. AdCMVLacZ (Q-BIOgene, Carisbad, Calif) infection was also found to induce apoptosis in HepG2 cells and significantly augment TRAIL-induced apoptosis. Anti-TRAIL antibody significantly inhibited apoptosis induced by AdCMVLacZ infection. Flow cytometry analysis revealed that both TRAIL-R2 and TRAIL were up-regulated on the cell surface of HepG2 cells with AdCMVLacZ infection. Transforming growth factor-beta1 also enhanced TRAIL expression in HepG2 cells. These results indicate that TRAIL/TRAIL-R apoptotic pathways play important roles in the hepatic cell death during viral infection.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)可诱导肿瘤细胞凋亡,但对大多数正常细胞无此作用。TRAIL在肝细胞死亡及肝脏疾病中的作用尚不清楚。本研究采用免疫组化法调查丙型肝炎病毒感染患者中TRAIL及TRAIL受体(TRAIL-Rs)的表达情况,并在HepG2细胞系中检测病毒感染情况下的生理作用。TRAIL或TRAIL-Rs在汇管区肝细胞的细胞质及细胞膜中染色显著。一些肝内浸润淋巴细胞对TRAIL也呈阳性染色。随着疾病进展,染色强度显著增加,尤其是在汇管区。还发现腺病毒CMV-LacZ(Q-BIOgene公司,加利福尼亚州卡尔斯巴德)感染可诱导HepG2细胞凋亡,并显著增强TRAIL诱导的凋亡。抗TRAIL抗体显著抑制腺病毒CMV-LacZ感染诱导的凋亡。流式细胞术分析显示,腺病毒CMV-LacZ感染时,HepG2细胞表面的TRAIL-R2和TRAIL均上调。转化生长因子-β1也增强了HepG2细胞中TRAIL的表达。这些结果表明,TRAIL/TRAIL-R凋亡途径在病毒感染期间的肝细胞死亡中起重要作用。

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