Literature DB >> 7844162

Imaging subcellular structures of rat mammary carcinoma cells by scanning force microscopy.

L I Pietrasanta1, A Schaper, T M Jovin.   

Abstract

Scanning force microscopy (SFM) was used for imaging subcellular structures of cultured rat mammary carcinoma cells dried in air. Identification of cellular substructures was achieved by immunofluorescence and specific fluorescence probes. Cells grown attached to a glass support exhibited submicrometer thickness in the dried state. Inside the nuclear domain the nucleoli appeared as prominent conical protrusions. Membrane extensions, microspikes and microvilli were well preserved at the cell periphery after fixation in glutaraldehyde vapor and air-drying and were distinguishable either as isolated elements or intercellular communications. The plasma membrane and soluble proteins were selectively removed with nonionic detergent in a buffer system. The mitochondria were concentrated primarily in the perinuclear space and exhibited a well defined filamentous shape. Their identity was confirmed by specific fluorescence staining with rhodamine 123. In the membrane-free system achieved by dry-cleaving of the sample surface, the cytoskeletal network was resolved as a complex mesh of actin-containing fiber bundles interwoven with a filigree arrangement of thinner filaments. The smallest fibrous substructures revealed by SFM with the scanning tips used to date were approximately 8 to 10 nm in height and 80 nm in width.

Entities:  

Mesh:

Year:  1994        PMID: 7844162     DOI: 10.1242/jcs.107.9.2427

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  8 in total

1.  Continuous wave two-photon scanning near-field optical microscopy.

Authors:  A K Kirsch; V Subramaniam; G Striker; C Schnetter; D J Arndt-Jovin; T M Jovin
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

2.  Targeted delivery of antibiotics to intracellular chlamydial infections using PLGA nanoparticles.

Authors:  Udaya S Toti; Bharath R Guru; Mirabela Hali; Christopher M McPharlin; Susan M Wykes; Jayanth Panyam; Judith A Whittum-Hudson
Journal:  Biomaterials       Date:  2011-06-08       Impact factor: 12.479

3.  Structure of the erythrocyte membrane skeleton as observed by atomic force microscopy.

Authors:  M Takeuchi; H Miyamoto; Y Sako; H Komizu; A Kusumi
Journal:  Biophys J       Date:  1998-05       Impact factor: 4.033

4.  Structural hierarchy in the clustering of HLA class I molecules in the plasma membrane of human lymphoblastoid cells.

Authors:  S Damjanovich; G Vereb; A Schaper; A Jenei; J Matkó; J P Starink; G Q Fox; D J Arndt-Jovin; T M Jovin
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-14       Impact factor: 11.205

5.  Picosecond multiphoton scanning near-field optical microscopy.

Authors:  A Jenei; A K Kirsch; V Subramaniam; D J Arndt-Jovin; T M Jovin
Journal:  Biophys J       Date:  1999-02       Impact factor: 4.033

6.  Flexible, actin-based ridges colocalise with the beta1 integrin on the surface of melanoma cells.

Authors:  K Poole; D Müller
Journal:  Br J Cancer       Date:  2005-04-25       Impact factor: 7.640

7.  High-speed atomic force microscopy combined with inverted optical microscopy for studying cellular events.

Authors:  Yuki Suzuki; Nobuaki Sakai; Aiko Yoshida; Yoshitsugu Uekusa; Akira Yagi; Yuka Imaoka; Shuichi Ito; Koichi Karaki; Kunio Takeyasu
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

8.  Morphological changes of plasma membrane and protein assembly during clathrin-mediated endocytosis.

Authors:  Aiko Yoshida; Nobuaki Sakai; Yoshitsugu Uekusa; Yuka Imaoka; Yoshitsuna Itagaki; Yuki Suzuki; Shige H Yoshimura
Journal:  PLoS Biol       Date:  2018-05-03       Impact factor: 8.029

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.