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疟原虫摄食过程的三维重建。

Three-dimensional reconstruction of the feeding process of the malaria parasite.

作者信息

Slomianny C

机构信息

Institut National de la Santé et de la Recherche Médicale, France.

出版信息

Blood Cells. 1990;16(2-3):369-78.

PMID:2096983
Abstract

The use of serial sectioning followed by three-dimensional (3D) reconstruction is a convenient way to study the spatial morphology of any structure (organ, cell, organelle). This method was applied to the study of the feeding mechanism of some strains of murine and human Plasmodium and enabled clarification of morphological features of this process. The feeding and digestive system of Plasmodium is polymorphic: in single sections, it shows rounded or elongated vesicles or vacuoles of very different sizes and content. The 3D reconstruction allowed us to describe the phenomenon both in space and in time. The contents of the host cell are taken up through the cytostome to form a sausage-shaped cytostomal tube. Individual digestive vesicles are either pinched off from the terminal portion of the tube or by the individualization of the different portions of the tube itself. The cytosomal system can be made of several tubes or vesicles always originating from cytostomes that can disappear when the tube is fully developed. A second feeding mechanism is also observed. Smaller vesicles are formed from the cytostomal vacuoles or tubes, or from the surface of the so-called "food vacuole, " or from the whole erythrocyte/parasite interface. Very few differences appear when the different strains are compared. In the chloroquine-resistant strain of P. berghei or in the P. falciparum FCR3 strain, there appears to be a large increase in the number of cytostomal vesicles, with several functional cytostomes in P. falciparum. The chronology of the appearance of the two systems is comparable between the different species except in P. falciparum, where the pigment vesicles fuse together very rapidly to form a large residual vacuole with which the subsequently formed and degraded digestive vacuoles fuse.

摘要

采用连续切片并进行三维(3D)重建是研究任何结构(器官、细胞、细胞器)空间形态的便捷方法。该方法被应用于研究某些鼠疟原虫和人疟原虫菌株的摄食机制,并有助于阐明这一过程的形态学特征。疟原虫的摄食和消化系统具有多态性:在单一切片中,它呈现出大小和内容物差异很大的圆形或细长形囊泡或液泡。三维重建使我们能够在空间和时间上描述这一现象。宿主细胞的内容物通过胞口被摄取,形成香肠状的胞口管。单个消化囊泡要么从管的末端部分 pinched off,要么通过管自身不同部分的个体化形成。胞口系统可以由几个总是起源于胞口的管或囊泡组成,当管完全发育时这些胞口可能会消失。还观察到另一种摄食机制。较小的囊泡由胞口液泡或管形成,或从所谓的“食物泡”表面形成,或从整个红细胞/寄生虫界面形成。比较不同菌株时几乎没有差异。在伯氏疟原虫的氯喹抗性菌株或恶性疟原虫FCR3菌株中,胞口囊泡的数量似乎大幅增加,恶性疟原虫中有几个功能性胞口。除了恶性疟原虫外,不同物种中这两种系统出现的时间顺序具有可比性,在恶性疟原虫中,色素囊泡迅速融合在一起形成一个大的残余液泡,随后形成并降解的消化液泡与之融合。 (注:pinched off 此处可能是“分离”之意,原文此处表述不太完整准确)

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