Hu Fengyu, Hu Xuchu, Ma Changling, Zhao Junhong, Xu Jin, Yu Xinbing
Department of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, PR China.
Mol Biochem Parasitol. 2009 Oct;167(2):127-34. doi: 10.1016/j.molbiopara.2009.05.003. Epub 2009 May 20.
A gene encoding a homologue of phospholipase A(2) was identified from the Clonorchis sinensis adult cDNA plasmid library. The deduced amino acid sequence including a signal peptide that has 28-46% identity with secretory phospholipase A(2), group III (group III sPLA(2)) of other species. It also has typical features of group III sPLA(2)s including 10 cysteines, the key residues of the Ca(2+) loop and catalytic site. The recombinant protein encoded by this gene expressed in Escherichia coli showed a product of about 34kDa in SDS-PAGE. Prediction of signal peptide and Western blot analysis indicated the group III secretory phospholipase A(2) of C. sinensis (CsGIIIsPLA(2)) was an excretory-secretory product (ES product). The enzyme activity of the recombinant protein was determined using phosphatidylcholine as substrates. The result revealed that the protein was a Ca(2+)-dependent PLA(2). Both MTT test and cell cycle analysis of LX-2 showed a higher percentage of cells are in proliferation phase. Semi-quantitative RT-PCR experiments demonstrated an up-regulated expression of collagen III in these cells after incubation with the recombinant protein. We also identified that the recombinant CsGIIIsPLA(2) could bind to some membrane proteins on LX-2 cells specifically by immunofluorescence, thus there might be receptors of CsGIIIsPLA(2) on the LX-2 cell membrane. Our results suggest that CsGIIIsPLA(2) might play an important role in the initiation and development of hepatic fibrosis caused by C. sinensis.
从华支睾吸虫成虫cDNA质粒文库中鉴定出一个编码磷脂酶A(2)同源物的基因。推导的氨基酸序列包括一个信号肽,与其他物种的分泌型磷脂酶A(2)Ⅲ组(Ⅲ组sPLA(2))具有28 - 46%的同一性。它还具有Ⅲ组sPLA(2)的典型特征,包括10个半胱氨酸、Ca(2+)环和催化位点的关键残基。该基因编码的重组蛋白在大肠杆菌中表达,在SDS - PAGE中显示出约34kDa的产物。信号肽预测和蛋白质印迹分析表明,华支睾吸虫的Ⅲ组分泌型磷脂酶A(2)(CsGIIIsPLA(2))是一种排泄 - 分泌产物(ES产物)。以磷脂酰胆碱为底物测定重组蛋白的酶活性。结果表明该蛋白是一种Ca(2+)依赖性磷脂酶A(2)。MTT试验和LX - 2细胞周期分析显示,处于增殖期的细胞百分比更高。半定量RT - PCR实验表明,用重组蛋白孵育后,这些细胞中Ⅲ型胶原的表达上调。我们还通过免疫荧光鉴定出重组CsGIIIsPLA(2)可以特异性结合LX - 2细胞上的一些膜蛋白,因此LX - 2细胞膜上可能存在CsGIIIsPLA(2)的受体。我们的结果表明,CsGIIIsPLA(2)可能在华支睾吸虫引起的肝纤维化的起始和发展中起重要作用。