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CYTOCHEMICAL DEMONSTRATION OF PEROXIDASE ACTIVITY WITH 3-AMINO-9-ETHYLCARBAZOLE.用3-氨基-9-乙基咔唑进行过氧化物酶活性的细胞化学显示
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AN ELECTRON MICROSCOPE STUDY OF THE AMOEBO-FLAGELLATE, NAEGLERIA GRUBERI (SCHARDINGER). I. THE AMOEBOID AND FLAGELLATE STAGES.阿米巴-鞭毛虫格氏耐格里原虫(沙尔丁格)的电子显微镜研究。I. 阿米巴型和鞭毛型阶段。
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Isolation, ultrastructure, and protein composition of the flagellar rootlet of Naegleria gruberi.格氏耐格里阿米巴鞭毛根丝体的分离、超微结构及蛋白质组成
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The detection of DNA-binding proteins by protein blotting.通过蛋白质印迹法检测DNA结合蛋白。
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Cell differentiation and flagellar elongation in Naegleria gruberi. Dependence on transcription and translation.格氏耐格里变形虫中的细胞分化与鞭毛伸长。对转录和翻译的依赖性。
J Cell Biol. 1980 May;85(2):346-60. doi: 10.1083/jcb.85.2.346.
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Control of flagellum number in Naegleria. Temperature shock induction of multiflagellate cells.纳格里亚属鞭毛数量的控制。多鞭毛细胞的温度休克诱导。
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格氏耐格里阿米巴鞭毛虫细胞骨架的合成与组装。

Synthesis and assembly of the cytoskeleton of Naegleria gruberi flagellates.

作者信息

Walsh C

出版信息

J Cell Biol. 1984 Feb;98(2):449-56. doi: 10.1083/jcb.98.2.449.

DOI:10.1083/jcb.98.2.449
PMID:6363422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2113116/
Abstract

When Naegleria gruberi flagellates were extracted with nonionic detergent and stained by the indirect immunofluorescence method with AA-4.3 (a monoclonal antibody against Naegleria beta-tubulin), flagella and a network of cytoskeletal microtubules (CSMT) were seen. When Naegleria amebae were examined in the same way, no cytoplasmic tubulin-containing structures were seen. Formation of the flagellate cytoskeleton was followed during the differentiation of amebae into flagellates by staining cells with AA-4.3. The first tubulin containing structures were a few cytoplasmic microtubules that formed at the time amebae rounded up into spherical cells. The formation of these microtubules was followed by the appearance of basal bodies and flagella and then by the formation of the CSMT. The CSMT formed before the cells assumed the flagellate shape. In flagellate shaped cells the CSMT radiate from the base of the flagella and follow a curving path the full length of the cell. Protein synthetic requirements for the formation of CSMT were examined by transferring cells to cycloheximide at various times after initiation. One-half the population completed the protein synthesis essential for formation of CSMT 61 min after initiation of the differentiation. This is 10 min after the time when protein synthesis for formation of flagella is completed and 10-15 min before the time when the protein synthesis necessary for formation of the flagellate shape is completed.

摘要

用非离子去污剂提取格氏耐格里阿米巴鞭毛虫,并采用间接免疫荧光法用AA - 4.3(一种抗耐格里阿米巴β - 微管蛋白的单克隆抗体)进行染色时,可观察到鞭毛和细胞骨架微管网络(CSMT)。当以同样的方式检查耐格里阿米巴变形虫时,未观察到含细胞质微管蛋白的结构。通过用AA - 4.3对细胞进行染色,在变形虫向鞭毛虫分化过程中追踪鞭毛虫细胞骨架的形成。最初含微管蛋白的结构是一些细胞质微管,它们在变形虫变圆形成球形细胞时形成。这些微管形成之后出现基体和鞭毛,然后形成CSMT。CSMT在细胞呈现鞭毛虫形状之前形成。在呈鞭毛虫形状的细胞中,CSMT从鞭毛基部放射状发出,并沿着细胞全长呈弯曲路径分布。通过在分化开始后的不同时间将细胞转移至环己酰亚胺来检查CSMT形成所需的蛋白质合成情况。在分化开始后61分钟,一半细胞群体完成了CSMT形成所必需的蛋白质合成。这比鞭毛形成所需蛋白质合成完成时间晚10分钟,比形成鞭毛虫形状所需蛋白质合成完成时间早10 - 15分钟。