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活跃细胞机制参与嗜热四膜虫无小核细胞口腔器的解体过程。

Involvement of active cellular mechanisms on the disorganization of oral apparatus in amicronucleate cells in Tetrahymena thermophila.

作者信息

Haremaki T, Sugai T, Takahashi M

机构信息

Institute of Biological Sciences, University of Tsukuba, Japan.

出版信息

Cell Struct Funct. 1996 Feb;21(1):73-80. doi: 10.1247/csf.21.73.

Abstract

Ciliated protozoa, a group of unicellular eukaryotes, have two kinds of nuclei, a macronucleus (somatic nucleus) and a micronucleus (germinal nucleus) in a single cell. We previously reported that amicronucleate cells of Tetrahymena thermophila induced by nocodazole gradually lost their oral apparatus (OA) and ciliary rows but that amacronucleate cells did not. Since the macronucleus is responsible for the gene expression in the vegetative phase, the effects of actinomycin D and cycloheximide on the disorganization of the OA in amicronucleate cells induced by nocodazole were investigated. These inhibitors prevented the disorganization of the OA in amicronucleate cells. Amicronucleate cells did not grow even in the medium supplemented with high concentration of Fe, Cu and folinic acid which allow cells to grow without formation of food vacuoles. The results suggest that the macronucleus in the amicronucleate cells plays an active role in the induction of disorganization of the OA and malfunctions of nutrient uptake from the cell surface and/or in the fundamental cell division mechanisms, resulting in the death of amicronucleate cells.

摘要

纤毛原生动物是一类单细胞真核生物,在单个细胞中具有两种细胞核,即大核(体细胞核)和小核(生殖细胞核)。我们之前报道过,诺考达唑诱导的嗜热四膜虫无小核细胞会逐渐失去其口器(OA)和纤毛列,但无大核细胞则不会。由于大核负责营养生长阶段的基因表达,因此研究了放线菌素D和环己酰亚胺对诺考达唑诱导的无小核细胞口器解体的影响。这些抑制剂阻止了无小核细胞口器的解体。即使在添加了高浓度铁、铜和亚叶酸的培养基中,无小核细胞也无法生长,而在这种培养基中细胞可以在不形成食物泡的情况下生长。结果表明,无小核细胞中的大核在口器解体的诱导以及从细胞表面摄取营养物质的功能障碍和/或基本细胞分裂机制中发挥着积极作用,从而导致无小核细胞死亡。

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