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微小膜蛋白MIC4或一种类似MIC4的蛋白,在刚地弓形虫的大配子体内表达,并与卵囊壁的形成有关。

The microneme protein MIC4, or an MIC4-like protein, is expressed within the macrogamete and associated with oocyst wall formation in Toxoplasma gondii.

作者信息

Ferguson D J, Brecht S, Soldati D

机构信息

Nuffield Department of Pathology, Oxford University, John Radcliffe Hospital, Oxford OX3 9DU, UK.

出版信息

Int J Parasitol. 2000 Oct;30(11):1203-9. doi: 10.1016/s0020-7519(00)00096-5.

Abstract

The expression and localisation of MIC4, or an immuno-cross reacting MIC4-like protein, was examined in the enteric forms of Toxoplasma gondii using immunocytochemistry. In addition to being located within the micronemes of the merozoites, MIC4 or the MIC4-like protein was present within the macrogamete and was associated with the developing oocyst wall. The macrogamete is characterised by two types of structurally distinct wall forming bodies (WFB1 and 2). However, by immuno-electron microscopy, it was possible to identify two populations of dense granules (WFB1) which appear to form sequentially during macrogamete development. The first granules to form (WFB1a) stained positively with anti-MIC4 and were followed by MIC4 negative granules (WFB1b). During oocyst wall formation, the WFB1a and b sequentially released their contents onto the surface with WFB1a material forming an anti-MIC4 positive outer veil, while the WFB1b forms the electron dense outer layer of the oocyst wall. The inner layer was formed by WFB2. Thus, for the first time, it was possible to identify two populations of dense granules (WFB1a and b) involved in the formation of different parts of the oocyst wall. It was not possible to analyse the contents of macrogametes by western blot to unequivocally identify the antigen recognised by the polyclonal antisera as MIC4.

摘要

利用免疫细胞化学技术,对弓形虫肠道型中MIC4或免疫交叉反应性MIC4样蛋白的表达和定位进行了检测。除了定位于裂殖子的微线体外,MIC4或MIC4样蛋白还存在于大配子内,并与发育中的卵囊壁相关。大配子的特征是有两种结构不同的壁形成体(WFB1和2)。然而,通过免疫电子显微镜观察,有可能识别出在大配子发育过程中似乎依次形成的两种致密颗粒群体(WFB1)。最早形成的颗粒(WFB1a)用抗MIC4抗体染色呈阳性,随后是MIC4阴性颗粒(WFB1b)。在卵囊壁形成过程中,WFB1a和b依次将其内容物释放到表面,WFB1a物质形成抗MIC4阳性的外层包膜,而WFB1b形成卵囊壁的电子致密外层。内层由WFB2形成。因此,首次有可能识别出参与卵囊壁不同部分形成的两种致密颗粒群体(WFB1a和b)。无法通过蛋白质印迹法分析大配子的内容物,以明确鉴定多克隆抗血清识别的抗原为MIC4。

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