| Literature DB >> 14722909 |
Gelsomina De Stasio1, Bradley H Frazer, Marco Girasole, Lisa M Wiese, Ewa K Krasnowska, Giulia Greco, Annalucia Serafino, Tiziana Parasassi.
Abstract
Established microscopies such as Scanning Electron Microscopy (SEM) and more recent developments such as Atomic Force Microscopy (AFM) and X-ray Photo-Electron Emission spectroMicroscopy (X-PEEM) can only image the sample surface. We present an argon sputtering method able to progressively expose inner cell structures without apparent damage. By varying the sputtering time, the structure of cell cytoskeleton, vesicles, mitochondria, nuclear membrane, and nucleoli can be imaged. We compared images obtained with confocal fluorescence microscopy, transmission electron microscopy (TEM), SEM, and X-PEEM on similar samples after argon sputtering, then confirmed the similarity of reference intracellular structures, including cytoskeleton fibers, cell-cell and cell-substrate adhesion structures, and secretory vesicles. We conclude that the sputtering method is a new valuable tool for surface sensitive microscopies. Copyright 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 14722909 DOI: 10.1002/jemt.20019
Source DB: PubMed Journal: Microsc Res Tech ISSN: 1059-910X Impact factor: 2.769