Wang Lingling, Zhang Huan, Wang Leilei, Zhang Daoxiang, Lv Zhao, Liu Zhaoqun, Wang Weilin, Zhou Zhi, Qiu Limei, Wang Hao, Li Jun, Song Linsheng
Liaoning Key Laboratory of Marine Animal Immunology & Disease Control, Dalian, 116023, China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, 266071, China.
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Dev Comp Immunol. 2017 Nov;76:209-219. doi: 10.1016/j.dci.2017.06.009. Epub 2017 Jun 20.
The complement system is one of the major effector mechanisms of immune system, playing essential roles in both the innate and adaptive immune responses. In the present study, the counterparts of vertebrate complement components were identified by screening the sequenced genome of Crassostrea gigas, resulting in the identification of 792 gene models containing complement-related domains. The transcriptome of haemocytes at 6, 12 and 24 h post lipopolysaccharides (LPS) stimulation showed differential expression of 77 C1q domain containing proteins, 53 C-type lectins and 42 fibrinogen-related proteins. mRNAs encoding 18 serine protease domain-containing (SPC) proteins, 4 MACPF-domain containing proteins and 11 C3 receptor-like proteins were up-regulated upon LPS stimulation, and CgC3 mRNA was significantly increased at 12 h. The presence of CgC3 was confirmed in cell free plasma and was present in three subunit chains as expected for the processed mature protein. The complement related PRRs with coiled coil regions and SPC proteins with CUB domains may function in the activation of CgC3, whereas, the C3-like receptors with integrin-α/β domain mediated the phagocytosis of C3-labled pathogens. These PRRs appear to serve as opsonins to promote phagocytosis of opsonized pathogens. The overall results suggested the existence of a potential multi-component complement system in C. gigas.
补体系统是免疫系统的主要效应机制之一,在固有免疫应答和适应性免疫应答中均发挥着重要作用。在本研究中,通过筛选太平洋牡蛎的测序基因组鉴定出脊椎动物补体成分的对应物,从而鉴定出792个含有补体相关结构域的基因模型。脂多糖(LPS)刺激后6、12和24小时血细胞的转录组显示,77种含C1q结构域的蛋白、53种C型凝集素和42种纤维蛋白原相关蛋白存在差异表达。编码18种含丝氨酸蛋白酶结构域(SPC)的蛋白、4种含MACPF结构域的蛋白和11种C3受体样蛋白的mRNA在LPS刺激后上调,且CgC3 mRNA在12小时时显著增加。在无细胞血浆中证实了CgC3的存在,并且如加工成熟蛋白所预期的那样,它以三条亚基链的形式存在。具有卷曲螺旋区域的补体相关模式识别受体(PRR)和具有CUB结构域的SPC蛋白可能在CgC3的激活中发挥作用,而具有整合素-α/β结构域的C3样受体介导了C3标记病原体的吞噬作用。这些PRR似乎作为调理素促进被调理病原体的吞噬作用。总体结果表明太平洋牡蛎中存在潜在的多组分补体系统。