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人肝硬化肝脏中小窝蛋白-1在蛋白质和mRNA水平的表达升高:与一氧化氮的关系

Elevated expression of caveolin-1 at protein and mRNA level in human cirrhotic liver: relation with nitric oxide.

作者信息

Yokomori Hiroaki, Oda Masaya, Yoshimura Kazunori, Nomura Masahiko, Wakabayashi Go, Kitajima Masaki, Ishii Hiromasa

机构信息

Department of Internal Medicine, Kitasato Institute Medical Center Hospital, 121-1 Arai, Kitamoto 364-8501, Japan.

出版信息

J Gastroenterol. 2003;38(9):854-60. doi: 10.1007/s00535-003-1161-4.

Abstract

BACKGROUND

Caveolin, the principal structural protein of caveolae, binds with endothelial nitric oxide synthase (eNOS) leading to enzyme inhibition. This study examined the expression of caveolin and eNOS at the protein and mRNA levels in patients with hepatocellular carcinoma and hepatitis C-related cirrhosis, and in control noncirrhotic liver specimens obtained from patients with metastatic liver carcinoma.

METHODS

Anti-eNOS, anti-caveolin-1, and anti-calmodulin antibodies were used for Western blotting. For in situ hybridization (ISH), human eNOS and caveolin-1 peptide nucleic acid probes were used with a catalyzed signal amplification system.

RESULTS

Western blotting showed marked overexpression of caveolin-1 protein in cirrhotic liver, while caveolin-1 was almost undetectable in control liver tissue. Endothelial NOS was expressed at a slightly higher level in cirrhotic liver than in control liver tissue. Calmodulin was expressed abundantly in control liver tissue and at a low level in cirrhotic liver tissue. By ISH, eNOS mRNA was localized on portal vein and hepatic lining cells, and caveolin-1 mRNA was almost undetectable in normal liver tissue. In cirrhotic liver tissue, caveolin-1 mRNA was overexpressed on hepatic sinusoidal lining cells, while eNOS mRNA expression was similar to that in normal liver.

CONCLUSIONS

Enhanced caveolin-1 expression may be associated with a significant reduction in NO catalytic activity in cirrhosis.

摘要

背景

小窝蛋白是小窝的主要结构蛋白,它与内皮型一氧化氮合酶(eNOS)结合导致酶活性受到抑制。本研究检测了肝细胞癌和丙型肝炎相关肝硬化患者以及转移性肝癌患者的非肝硬化肝脏对照标本中小窝蛋白和eNOS在蛋白质和mRNA水平的表达情况。

方法

使用抗eNOS、抗小窝蛋白-1和抗钙调蛋白抗体进行蛋白质印迹分析。对于原位杂交(ISH),使用人eNOS和小窝蛋白-1肽核酸探针以及催化信号放大系统。

结果

蛋白质印迹分析显示,小窝蛋白-1蛋白在肝硬化肝脏中明显过表达,而在对照肝脏组织中几乎检测不到。内皮型一氧化氮合酶在肝硬化肝脏中的表达水平略高于对照肝脏组织。钙调蛋白在对照肝脏组织中大量表达,在肝硬化肝脏组织中表达水平较低。通过原位杂交,eNOS mRNA定位于门静脉和肝内衬细胞,而在正常肝脏组织中几乎检测不到小窝蛋白-1 mRNA。在肝硬化肝脏组织中,小窝蛋白-1 mRNA在肝窦内衬细胞上过表达,而eNOS mRNA表达与正常肝脏相似。

结论

小窝蛋白-1表达增强可能与肝硬化中NO催化活性显著降低有关。

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