Real-time PCR quantification of the in vitro effects of crustacean immunostimulants on gene expression in lobster (Homarus gammarus) granular haemocytes

被引:47
作者
Hauton, C [1 ]
Hammond, JA [1 ]
Smith, VJ [1 ]
机构
[1] Univ St Andrews, Sch Biol, Gatty Marine Lab, Comparat Immunol Grp, St Andrews KY16 8LB, Fife, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
real-time PCR; immunostimulants; prophenoloxidase; beta-1,3-glucan binding protein; lobster; Homarus gammarus; granulocytes;
D O I
10.1016/j.dci.2004.05.006
中图分类号
S9 [水产、渔业];
学科分类号
0908 [水产];
摘要
This paper presents data from an investigation of the mode of action of five different crustacean immunostimulants presented to European lobster (Homarus gammarus) granulocytes cultured in vitro. The experiments were designed to test whether or not the immunostimulants could cause the short-term up-regulation of genes coding for immune proteins without causing the cells to degranulate. Quantitative measurements of mRNA transcript abundance were made using real-time PCR and it was first necessary to isolate the complete gene sequences coding for the proteins prophenoloxidase (proPO), beta-1,3-glucan binding protein (betaGBP) and beta-actin (beta-act) in the lobster. These sequences were used to design TaqMan(TM) primer and fluorescent probe sets. The presented data indicated that the majority of the tested immunostimulants did not induce the up-regulation of immune-related gene expression in the granulocytes in isolation. Alternative modes of action, including the in vivo up-regulation of gene expression in haemopoetic tissues, are discussed. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 42
页数:10
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