Structural and molecular biological study of duplication of centrioles during ciliogenesis
Structural and molecular biological study of duplication of centrioles during ciliogenesis
批准号:
14570002
负责人:
HAGIWARA Haruo
金额:
$2.24万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003
中文摘要
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英文摘要
In most animal cells, the Golgi apparatus is located in the juxtanuclear region and appears almost stationary around the centrosome. The centrosome, consisting of a pair of centrioles and the centrosomal matrix, nucleates microtubules. Several Golgi matrix proteins including TGN 38 and golgin-97 have been reported to be localized to the centrosome throughout the cell cycle, but localization of Golgi 58K protein to the centrosome has not been studied as yet. In the present study, we investigated the localization of Golgi 58K protein in MDCK, KD, and HeLa cells and in the oviductal columnar epithelium of human and experimental animals. Localization of Golgi proteins to centrioles was investigated with structural and cell biological methods.The centrosome was positively stained with anti Golgi 58K antibodies in MDCK, KD and HeLa cells. Golgi 58K remained associated with the centrosome throughout the cell cycle. Association of Golgi 58K to the centrosome was not disturbed by the colcemid or brefeldin A treatment. Cold treatment also had no effect on the association of Golgi 58K to the centrosome. The oviduct epithelium mainly consisted of ciliated cells and secretory cells with or without primary cilia. The centrosome located in the apical region of columnar epithelial cells and basal bodies extending cilia were positively stained with Golgi 58K. These observations indicate that centrioles are maintained within the matrix containing common molecules to the Golgi apparatus, even after the migration to the apical cytoplasm and or formation of cilia. Golgi matrix proteins might have important roles on duplication of centrioles during ciliogenesis.
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萩原治夫(分担執筆): "初めてでもできる共焦点顕微鏡活用プロトコール:多重染色法"羊土社. 217(70-77) (2004)
Haruo Hagiwara(合著者):“初学者共聚焦显微镜方案:多重染色方法”Yodosha 217(70-77)(2004)。
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萩原治夫: "線毛のルートレット"ミクロスコピア. 20・4. 20-21 (2004)
Haruo Hagiwara:“纤毛根”显微镜 20・4(2004)。
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Shinoda Y, Matsuzaki T, Yokoo-Sugawara M, Hagiwara H, et al.: "Induction and Expression of Glucose Transporters in Pancreatic Acinar Cells by In Vitro Elecroporation."Acta Histochemica et Cytochemica. 36・1. 77-82 (2003)
Shinoda Y、Matsuzaki T、Yokoo-Sugara M、Hagiwara H 等:“通过体外电穿孔在胰腺腺泡细胞中诱导和表达葡萄糖转运蛋白”。Acta Histochemica et Cytochemica 36·1(2003)。
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Hagiwara H, Ohwada N, Takata K: "Cell biology of normal and abnormal ciliogenesis in the ciliated epithelium."International review of cytology. 234. 101-141 (2004)
Hagiwara H、Ohwada N、Takata K:“纤毛上皮中正常和异常纤毛发生的细胞生物学。”国际细胞学评论。
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Takata K, Takahashi Y, Matsuzaki T, Tajika Y, Hagiwara H et al.: "A simple electroporation method for the introduction of plasmids into cells cultured on coverslips for histochemical examination."Acta Histochemica et Cytochemica. 36・4. 317-323 (2003)
Takata K、Takahashi Y、Matsuzaki T、Tajika Y、Hagiwara H 等人:“一种将质粒引入盖玻片上培养的细胞中进行组织化学检查的简单电穿孔方法。”Acta Histochemica et Cytochemica 36・4。 (2003)
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共 10 条
The mechanism of elongation of primary cilia from basal bodies in ciliogenesis
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