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鉴定秀丽隐杆线虫的 24kDa 分泌蛋白。

Identification of a 24 kDa excretory secretory protein in Anisakis simplex.

机构信息

Department of Urology, School of Medicine, Pusan National University, Yangsan-si, Gyeongsannam-do 626-870, Republic of Korea.

出版信息

Exp Parasitol. 2012 Jan;130(1):69-72. doi: 10.1016/j.exppara.2011.09.008.

Abstract

A gene coding for a 24 kDa protein (22 U homologous; As22U) was isolated from the Anisakis simplex third-stage larvae cDNA library during expressed sequence tag analysis. As22U was 636 bp long, and was found to code for 212 amino acid residues with a calculated mass of 23.5 kDa and a PI of 9.06. The As22U deduced amino acid sequence harbored a signal peptide region and 16 highly conserved cysteine residues, and it was identified in both the total extracts and excretory secretory (ES) protein of A. simplex. Its molecular weight was measured at 24 kDa via western blot analysis. The expression levels of thymic stromal lymphopoietin, IL-25, and CXCL1 (Gro-α) genes were increased at 6h after recombinant As22U treatment in mouse intestinal epithelial cells. Additionally, thymus and activation-regulated chemokine gene levels were increased at 14 h after treatment. Although we do not currently have sufficient evidence to determine whether As22U plays a role as an allergen, this remains possible. Further in vivo studies may provide some insight as to the allergenic properties of As22U.

摘要

从秀丽隐杆线虫第三期幼虫 cDNA 文库的表达序列标签分析中分离出编码 24 kDa 蛋白(22 U 同源物;As22U)的基因。As22U 长 636 bp,编码 212 个氨基酸残基,计算分子量为 23.5 kDa,PI 为 9.06。As22U 推断的氨基酸序列含有一个信号肽区域和 16 个高度保守的半胱氨酸残基,在秀丽隐杆线虫的总提取物和分泌蛋白中都有发现。通过 Western blot 分析,其分子量测定为 24 kDa。重组 As22U 处理后,在小鼠肠上皮细胞中,胸腺基质淋巴细胞生成素、IL-25 和 CXCL1(Gro-α)基因的表达水平在 6 小时后增加,而在 14 小时后,胸腺和激活调节趋化因子基因水平增加。虽然我们目前还没有足够的证据来确定 As22U 是否作为过敏原发挥作用,但这种可能性仍然存在。进一步的体内研究可能会提供一些关于 As22U 过敏原特性的见解。

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