Transcriptomic and Quantitative Proteomic Analyses Provide Insights Into the Phagocytic Killing of Hemocytes in the Oyster Crassostrea gigas
Jiang, Shuai1; Qiu, Limei1; Wang, Lingling2; Jia, Zhihao1,3; Lv, Zhao1,3; Wang, Mengqiang1; Liu, Conghui1,3; Xu, Jiachao1,3; Song, Linsheng2
刊名FRONTIERS IN IMMUNOLOGY
2018-06-11
卷号9页码:17
关键词Crassostrea gigas transcriptome quantitative proteome phagocyte oxidative killing lysosome cathepsin L
ISSN号1664-3224
DOI10.3389/fimmu.2018.01280
通讯作者Wang, Lingling(wanglingling@dlou.edu.cn)
英文摘要As invertebrates lack an adaptive immune system, they depend to a large extent on their innate immune system to recognize and clear invading pathogens. Although phagocytes play pivotal roles in invertebrate innate immunity, the molecular mechanisms underlying this killing remain unclear. Cells of this type from the Pacific oyster Crassostrea gigas were classified efficiently in this study via fluorescence-activated cell sorting (FACS) based on their phagocytosis of FITC-labeled latex beads. Transcriptomic and quantitative proteomic analyses revealed a series of differentially expressed genes (DEGs) and proteins present in phagocytes; of the 352 significantly high expressed proteins identified here within the phagocyte proteome, 262 corresponding genes were similarly high expressed in the transcriptome, while 140 of 205 significantly low expressed proteins within the proteome were transcriptionally low expressed. A pathway crosstalk network analysis of these significantly high expressed proteins revealed that phagocytes were highly activated in a number of antimicrobial-related biological processes, including oxidation-reduction and lysosomal proteolysis processes. A number of DEGs, including oxidase, lysosomal protease, and immune receptors, were also validated in this study using quantitative PCR, while seven lysosomal cysteine proteases, referred to as cathepsin Ls, were significantly high expressed in phagocytes. Results show that the expression level of cathepsin L protein in phagocytes [mean fluorescence intensity (MFI): 327 +/- 51] was significantly higher (p < 0.01) than that in non-phagocytic hemocytes (MFI: 83 +/- 26), while the cathepsin L protein was colocalized with the phagocytosed Vibrio splendidus in oyster hemocytes during this process. The results of this study collectively suggest that oyster phagocytes possess both potent oxidative killing and microbial disintegration capacities; these findings provide important insights into hemocyte phagocytic killing as a component of C. gigas innate immunity.
资助项目Natural Science Foundation of China[31530069] ; Natural Science Foundation of China[41406170] ; Qingdao National Laboratory for Marine Science and Technology[2017ASTCP-OS13] ; 863 Program[2014AA103501] ; for Modern Agro-industry Technology Research System[CARS-49] ; Dalian High Level Talent Innovation Support Program[2015R020] ; Research Foundation for Distinguished Professor in Liaoning ; Talented Scholars in Dalian Ocean University
WOS研究方向Immunology
语种英语
出版者FRONTIERS MEDIA SA
WOS记录号WOS:000434796400001
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/159202]  
专题海洋研究所_实验海洋生物学重点实验室
通讯作者Wang, Lingling
作者单位1.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao, Peoples R China
2.Dalian Ocean Univ, Liaoning Key Lab Marine Anim Immunol & Dis Contro, Dalian, Peoples R China
3.Univ Chinese Acad Sci, Beijing, Peoples R China
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Jiang, Shuai,Qiu, Limei,Wang, Lingling,et al. Transcriptomic and Quantitative Proteomic Analyses Provide Insights Into the Phagocytic Killing of Hemocytes in the Oyster Crassostrea gigas[J]. FRONTIERS IN IMMUNOLOGY,2018,9:17.
APA Jiang, Shuai.,Qiu, Limei.,Wang, Lingling.,Jia, Zhihao.,Lv, Zhao.,...&Song, Linsheng.(2018).Transcriptomic and Quantitative Proteomic Analyses Provide Insights Into the Phagocytic Killing of Hemocytes in the Oyster Crassostrea gigas.FRONTIERS IN IMMUNOLOGY,9,17.
MLA Jiang, Shuai,et al."Transcriptomic and Quantitative Proteomic Analyses Provide Insights Into the Phagocytic Killing of Hemocytes in the Oyster Crassostrea gigas".FRONTIERS IN IMMUNOLOGY 9(2018):17.
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