Literature DB >> 2584910

Three-dimensional studies of cytoskeletal organizations in cultured thyroid cells by quick-freezing and deep-etching method.

S Ohno, N Takasu.   

Abstract

Isolated porcine thyroid cells were cultured on collagen gels (control group, TSH-stimulated group, and double-layered culture). They were split or cut to remove cytoplasmic soluble proteins for replica preparations. Some specimens were immunostained with anti-actin antibody or decorated with S1 myosin fragments to identify actin filaments. The basal cell membranes of thyroid cells of monolayer culture were in contact with collagen gels and the apical cell membranes faced the culture medium. Networks of actin filaments were attached to the cytoplasmic sides of the apical cell membranes, while intermediate filaments were localized along the basal ones. The thyroid-stimulating hormone (TSH) treatment induced the formation of microvilli only on the apical cell membranes and the accumulation of actin filaments under the apical cell membranes, indicating the apical-basal polarity of the cells. In double-layered culture, the primitive follicular lumens with microvilli appeared between two adjacent cells. The interaction of cell membranes with collagen gels is a determinant factor in the orientation of apical-basal polarity. Moreover, the TSH treatment and cell-cell contact further intensify the polarization through reorganizing the cytoskeletons.

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Year:  1989        PMID: 2584910

Source DB:  PubMed          Journal:  J Electron Microsc (Tokyo)        ISSN: 0022-0744


  8 in total

1.  An ultrastructural study of the cytoplasmic aspects of erythrocyte membranes by a quick-freezing and deep-etching method.

Authors:  S Ohno
Journal:  J Anat       Date:  1992-04       Impact factor: 2.610

2.  Three-dimensional studies of the cytoskeleton of cultured hepatocytes: a quick-freezing and deep-etching study.

Authors:  S Ohno; Y Fujii
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

3.  Three-dimensional ultrastructure of glomerular injury in serum sickness nephritis using the quick-freezing and deep-etching method.

Authors:  A Naramoto; S Ohno; K Nakazawa; H Takami; N Itoh; H Shigematsu
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

4.  Immunocytochemical study of membrane skeletons in abnormally shaped erythrocytes as revealed by a quick-freezing and deep-etching method.

Authors:  S Ohno; N Terada; Y Fujii; H Ueda; H Kuramoto; N Kamisawa
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

5.  Immunocytochemical study of dystrophin in cultured mouse muscle cells by the quick-freezing and deep-etching method.

Authors:  Y C Park-Matsumoto; S Ohno; T Baba; T Kobayashi; H Tsukagoshi
Journal:  Histochem J       Date:  1992-06

6.  Localization of laminin in nephritic glomeruli as revealed by a quick-freezing and deep-etching method with immunohistochemistry.

Authors:  A Naramoto; S Ohno; N Itoh; N Shibata; H Shigematsu
Journal:  Histochem J       Date:  1992-10

7.  Ultrastructure of matriceal changes in chronic phase of Masugi nephritis by quick-freezing and deep-etching method.

Authors:  A Naramoto; S Ohno; N Itoh; N Shibata; K Nakazawa; H Takami; H J Duan; H Kasahara; H Shigematsu
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

8.  Three-dimensional ultrastructure of anionic sites of the glomerular basement membrane by a quick-freezing and deep-etching method using a cationic tracer.

Authors:  A Yoshimura; S Ohno; K Nakano; H Oniki; K Inui; T Ideura; S Koshikawa
Journal:  Histochemistry       Date:  1991
  8 in total

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