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J Hepatol. 2016 Feb;64(2):352-360. doi: 10.1016/j.jhep.2015.09.025. Epub 2015 Oct 8.
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β-Adrenergic receptors stimulate interleukin-6 production through Epac-dependent activation of PKCδ/p38 MAPK signalling in neonatal mouse cardiac fibroblasts.β-肾上腺素能受体通过 Epac 依赖性激活 PKCδ/p38 MAPK 信号通路促进新生鼠心肌成纤维细胞白细胞介素 6 的产生。
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PLCγ2 通过 PKCD/JNK MAPK 和 PKCD/p38 MAPK 信号通路促进大鼠肝细胞凋亡,抑制增殖。

PLCγ2 promotes apoptosis while inhibits proliferation in rat hepatocytes through PKCD/JNK MAPK and PKCD/p38 MAPK signalling.

机构信息

Animal Science and Technology School, Henan University of Science and Technology, Luoyang, China.

出版信息

Cell Prolif. 2018 Jun;51(3):e12437. doi: 10.1111/cpr.12437. Epub 2018 Feb 11.

DOI:10.1111/cpr.12437
PMID:29430764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6528867/
Abstract

OBJECTIVES

The PLCG2 (PLCγ2) gene is a member of PLC gene family encoding transmembrane signalling enzymes involved in various biological processes including cell proliferation and apoptosis. Our earlier study indicated that PLCγ2 may be involved in the termination of regeneration of the liver which is mainly composed of hepatocytes, but its exact biological function and molecular mechanism in liver regeneration termination remains unclear. This study aims to examine the role of PLCγ2 in the growth of hepatocytes.

MATERIALS AND METHODS

A recombinant adenovirus expressing PLCγ2 was used to infect primary rat hepatocytes. PLCγ2 mRNA and protein levels were detected by qRT-PCR and Western blot. The subcellular location of PLCγ2 protein was tested by an immunofluorescence assay. The proliferation of hepatocytes was measured by MTT assay. The cell cycle and apoptosis were analysed by flow cytometry. Caspase-3, -8 and -9 activities were measured by a spectrophotometry method. Phosphorylation levels of PKCD, JNK and p38 in the infected cells were detected by Western blot. The possible mechanism underlying the role of PLCγ2 in hepatocyte growth was also explored by adding a signalling pathway inhibitor.

RESULTS

Hepatocyte proliferation was dramatically reduced, while cell apoptosis was remarkably increased. The results demonstrated that PLCγ2 increased the phosphorylation of PKCD, p38 and JNK in rat hepatocytes. After PKCD activity was inhibited by the inhibitor Go 6983, the levels of both p-p38 and p-JNK MAPKs significantly decreased, and PLCγ2-induced cell proliferation inhibition and cell apoptosis were obviously reversed.

CONCLUSIONS

This study showed that PLCγ2 regulates hepatocyte growth through PKCD-dependently activating p38 MAPK and JNK MAPK pathways; this result was experimentally based on the further exploration of the effect of PLCγ2 on hepatocyte growth in vivo.

摘要

目的

PLCγ2(PLCγ2)基因是 PLC 基因家族的成员,编码参与多种生物过程的跨膜信号酶,包括细胞增殖和细胞凋亡。我们之前的研究表明,PLCγ2 可能参与肝脏再生的终止,肝脏主要由肝细胞组成,但 PLCγ2 在肝脏再生终止中的确切生物学功能和分子机制尚不清楚。本研究旨在研究 PLCγ2 在肝细胞生长中的作用。

材料和方法

使用表达 PLCγ2 的重组腺病毒感染原代大鼠肝细胞。通过 qRT-PCR 和 Western blot 检测 PLCγ2 mRNA 和蛋白水平。通过免疫荧光测定检测 PLCγ2 蛋白的亚细胞定位。通过 MTT 测定法测量肝细胞的增殖。通过流式细胞术分析细胞周期和细胞凋亡。通过分光光度法测定 caspase-3、-8 和 -9 的活性。通过 Western blot 检测感染细胞中 PKCD、JNK 和 p38 的磷酸化水平。还通过添加信号通路抑制剂来探索 PLCγ2 在肝细胞生长中的作用的可能机制。

结果

肝细胞增殖明显减少,而细胞凋亡明显增加。结果表明,PLCγ2 增加了大鼠肝细胞中 PKCD、p38 和 JNK 的磷酸化。用抑制剂 Go 6983 抑制 PKCD 活性后,p-p38 和 p-JNK MAPKs 的水平显著降低,PLCγ2 诱导的细胞增殖抑制和细胞凋亡明显逆转。

结论

本研究表明,PLCγ2 通过依赖 PKCD 的方式调节肝细胞生长,激活 p38 MAPK 和 JNK MAPK 通路;这一结果是在进一步探索 PLCγ2 对体内肝细胞生长的影响的基础上得出的。