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在乙型肝炎病毒感染期间,载脂蛋白 M 水平升高会反馈抑制乙型肝炎病毒复制。

Enchanced levels of apolipoprotein M during HBV infection feedback suppresses HBV replication.

机构信息

Center for Gene Diagnosis, Zhongnan Hospital, Wuhan University, PR China.

出版信息

Lipids Health Dis. 2011 Aug 29;10:154. doi: 10.1186/1476-511X-10-154.

Abstract

BACKGROUND

Chronic liver diseases can interfere with hepatic metabolism of lipoproteins, apolipoproteins. Hepatitis B virus (HBV) is a major etiological agent causing acute and chronic liver diseases. Apolipoprotein M (ApoM) is a high-density lipoprotein (HDL) apolipoprotein and exclusively expressed in the liver parenchyma cells and in the tubular cells of the kidney. This study was to determine the correlation between HBV infection and ApoM expression.

MATERIALS AND METHODS

Serum ApoM levels in patients with HBV infection and in healthy individuals were measured by ELISA, ApoM mRNA expression were determined by RT-PCR, and the expression of S and E proteins of HBV, as well as the synthesis of viral DNA were measured by ELISA and real-time PCR.

RESULTS

The levels of serum ApoM was significantly elevated in patients as compared to healthy individuals (P < 0.001), ApoM promoter activity, mRNA and protein expression were all stimulated in cells transfected with infectious HBV clone. In addition, ApoM decreases the expression of S and E proteins of HBV and the synthesis of viral DNA.

CONCLUSION

Raised ApoM levels in HBV infection may in turn suppress HBV replication, one of the protective mechanisms of nature.

摘要

背景

慢性肝脏疾病可干扰脂蛋白、载脂蛋白的肝脏代谢。乙型肝炎病毒(HBV)是引起急性和慢性肝脏疾病的主要病因。载脂蛋白 M(ApoM)是一种高密度脂蛋白(HDL)载脂蛋白,仅在肝实质细胞和肾脏的管状细胞中表达。本研究旨在确定 HBV 感染与 ApoM 表达之间的相关性。

材料和方法

采用 ELISA 法检测 HBV 感染患者和健康个体的血清 ApoM 水平,采用 RT-PCR 法检测 ApoM mRNA 表达,采用 ELISA 和实时 PCR 法检测 HBV 的 S 和 E 蛋白的表达以及病毒 DNA 的合成。

结果

与健康个体相比,患者的血清 ApoM 水平显著升高(P < 0.001),转染感染性 HBV 克隆的细胞中 ApoM 启动子活性、mRNA 和蛋白表达均受到刺激。此外,ApoM 降低了 HBV 的 S 和 E 蛋白的表达和病毒 DNA 的合成。

结论

HBV 感染中升高的 ApoM 水平可能反过来抑制 HBV 复制,这是自然的一种保护机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9ee/3173363/7b5846b9bb91/1476-511X-10-154-1.jpg

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