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植物糖蛋白(24千道尔顿)通过蛋白激酶Cα和丝裂原活化蛋白激酶抑制氧自由基刺激的张氏肝细胞中增殖细胞核抗原的表达。

Phytoglycoprotein (24 kDa) inhibits expression of PCNA via PKCalpha and MAPKs in oxygen radical-stimulated Chang liver cells.

作者信息

Lee Sei-Jung, Lim Kye-Taek

机构信息

Molecular Biochemistry Laboratory, Biotechnology Research Institute and Center for the Control of Animal Hazards Using Biotechnology (BK 21), Chonnam National University, Kwang-ju 500-757, South Korea.

出版信息

J Nutr Biochem. 2009 Feb;20(2):96-105. doi: 10.1016/j.jnutbio.2007.12.004. Epub 2008 May 27.

DOI:10.1016/j.jnutbio.2007.12.004
PMID:18508255
Abstract

The purpose of this study was to investigate the inhibitory effect of 24-kDa glycoprotein isolated from Zanthoxylum piperitum DC fruit (ZPDC glycoprotein) on glucose/glucose oxidase (G/GO)- or hypoxanthine/xanthine oxidase (HX/XO)-induced cell proliferation in Chang liver cells. We found that ZPDC glycoprotein has significant scavenging effect on the production of intracellular H2O2 without cytotoxicity in G/GO- or HX/XO-treated in Chang liver cells. In the G/GO or HX/XO-stimulated protein kinases activity, ZPDC glycoprotein inhibited translocation of protein kinase C alpha (PKCalpha) to membrane and phosphorylation of extracellular signal-regulated kinase, p38 MAP kinase and c-Jun N-terminal kinase, respectively. In the G/GO or HX/XO-stimulated transcriptional activity, ZPDC glycoprotein also blocked the DNA binding activities of nuclear factor-kappa B and activator protein-1 and attenuated the activities of p50, p65, c-Jun and c-Fos, respectively. Finally, in the G/GO or HX/XO-stimulated cell proliferation, the activity of proliferating cell nuclear antigen was significantly blocked by treatment with ZPDC glycoprotein as well as protein kinase C inhibitor and mitogen-activated protein kinase inhibitors. On the basis of these results, we speculate that this glycoprotein is one of the natural antioxidants and of the modulators on abnormal activation of cell proliferation-related molecules in Chang liver cells.

摘要

本研究旨在探讨从花椒果实中分离出的24 kDa糖蛋白(ZPDC糖蛋白)对葡萄糖/葡萄糖氧化酶(G/GO)或次黄嘌呤/黄嘌呤氧化酶(HX/XO)诱导的Chang肝细胞增殖的抑制作用。我们发现,ZPDC糖蛋白对G/GO或HX/XO处理的Chang肝细胞内H2O2的产生具有显著的清除作用,且无细胞毒性。在G/GO或HX/XO刺激的蛋白激酶活性方面,ZPDC糖蛋白分别抑制蛋白激酶Cα(PKCalpha)向膜的转位以及细胞外信号调节激酶、p38丝裂原活化蛋白激酶和c-Jun氨基末端激酶的磷酸化。在G/GO或HX/XO刺激的转录活性方面,ZPDC糖蛋白还阻断了核因子-κB和活化蛋白-1的DNA结合活性,并分别减弱了p50、p65、c-Jun和c-Fos的活性。最后,在G/GO或HX/XO刺激的细胞增殖中,ZPDC糖蛋白以及蛋白激酶C抑制剂和丝裂原活化蛋白激酶抑制剂处理均显著阻断了增殖细胞核抗原的活性。基于这些结果,我们推测这种糖蛋白是天然抗氧化剂之一,也是Chang肝细胞中细胞增殖相关分子异常激活的调节剂。

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