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Cited 15 time in webofscience Cited 16 time in scopus
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Innate immune response in the hemolymph of an ascidian, Halocynthia roretzi, showing soft tunic syndrome, using label-free quantitative proteomics

Authors
Cha, In Seokdel Castillo, Carmelo SegoviaNho, Seong WonHikima, Jun-ichiAoki, TakashiJung, Tae Sung
Issue Date
Aug-2011
Publisher
ELSEVIER SCI LTD
Keywords
Soft tunic syndrome; Halocynthia roretzi; Innate immunity; Label-free quantitative proteomics; Hemolymph
Citation
Developmental and Comparative Immunology, v.35, no.8, pp 809 - 816
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
Developmental and Comparative Immunology
Volume
35
Number
8
Start Page
809
End Page
816
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/23642
DOI
10.1016/j.dci.2011.01.011
ISSN
0145-305X
1879-0089
Abstract
Soft tunic syndrome of Halocynthia roretzi manifests as soft, weak, and rupturable tunics, causing mass mortality. Utilizing liquid chromatography-tandem mass spectrometry (LC-MS/MS), innate immune response was established by comparing hemolymph protein profiles of ascidians with healthy or softened tunics. Of 100 proteins in each individual ascidian, 59 proteins from healthy and 56 proteins from diseased ascidians were functionally classified. Proteins found only in diseased individuals included trypsin inhibitor and Hr-29, and with high exponentially modified protein abundance index (emPAI) values. From 41 proteins identified to be common to both healthy and diseased ascidians, 15 were associated with innate immune response. Ficolin 3, a component of the lectin-complement system, was significantly decreased in diseased ascidians, but a cell surface protein, type II transmembrane serine protease-1 (TTSP), was considerably elevated. These results suggest that trypsin inhibitor, ficolin 3, and TTSP are probably involved in the innate immune response related to this tunic disease. Beside. Hr-29 could be suggested as a biomarker for soft tunic syndrome. (C) 2011 Elsevier Ltd. All rights reserved.
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