Laboratory of Pathology and Immunology of Aquatic Animals, KLMME, Ocean University of China, Qingdao 266003, PR China.
Laboratory of Pathology and Immunology of Aquatic Animals, KLMME, Ocean University of China, Qingdao 266003, PR China.
Fish Shellfish Immunol. 2018 Jan;72:325-333. doi: 10.1016/j.fsi.2017.09.074. Epub 2017 Sep 28.
In our previous work, granulocytes and hyalinocytes were successfully separated by immunomagnetic bead (IMB) method using monoclonal antibodies (mAbs) against granulocytes of shrimp (Fenneropenaeus chinensis). In order to elucidate the proteomic differentiation between granulocytes and hyalinocytes, in this paper, the differentially expressed proteins were analyzed between non-fixed/un-permeabilized (NFP) haemocytes and fixed/permeabilized (FP) haemocytes using two-dimensional gel electrophoresis (2-DE) combined with mass spectrometry (MS). Then the FP haemocytes were separated into two haemocyte subpopulations using IMB method, and the comparative proteome between granulocytes and hyalinocytes was investigated. The results showed that 10 differentially expressed protein spots were detected and identified as 4 proteins in the NFP haemocytes. Twenty one differentially expressed proteins were successfully identified between granulocytes and hyalinocytes, which include 4 unique expressed proteins in granulocytes, 4 significantly highly expressed proteins in granulocytes, and 13 significantly high expressed proteins in hyalinocytes. According to Gene Ontology annotation, the identified proteins between granulocytes and hyalinocytes were classified into six categories, including binding proteins, proteins involved in catalytic activity, enzyme regulator activity, structural molecule activity, translation regulator activity, and ungrouped proteins. Furthermore, quantitative PCR confirmed that the trend of transcription levels of three selected genes were consistent with the proteomic data from 2-DE. The results may lead to better understanding of the functions of haemocyte subpopulations.
在我们之前的工作中,使用针对中国对虾(Fenneropenaeus chinensis)粒细胞的单克隆抗体(mAbs),通过免疫磁珠(IMB)方法成功地分离了粒细胞和透明细胞。为了阐明粒细胞和透明细胞之间的蛋白质组学差异,本文使用二维凝胶电泳(2-DE)结合质谱(MS)分析了非固定/未通透(NFP)血细胞和固定/通透(FP)血细胞之间差异表达的蛋白质。然后使用 IMB 方法将 FP 血细胞分离成两个血细胞亚群,并研究了粒细胞和透明细胞之间的比较蛋白质组学。结果表明,在 NFP 血细胞中检测到并鉴定出 10 个差异表达的蛋白质斑点。在粒细胞和透明细胞之间成功鉴定出 21 个差异表达的蛋白质,其中粒细胞中有 4 个独特表达的蛋白质,粒细胞中 4 个表达显著上调的蛋白质,透明细胞中有 13 个表达显著上调的蛋白质。根据基因本体注释,在粒细胞和透明细胞之间鉴定出的蛋白质分为 6 类,包括结合蛋白、催化活性相关蛋白、酶调节活性相关蛋白、结构分子活性相关蛋白、翻译调节活性相关蛋白和未分类蛋白。此外,定量 PCR 证实了三个选定基因的转录水平趋势与 2-DE 的蛋白质组学数据一致。这些结果可能有助于更好地理解血细胞亚群的功能。