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Cell-substrate contacts illuminated by total internal reflection fluorescence
A technique for exciting fluorescence exclusively from regions of contact between cultured cells and the substrate is presented. The technique utilizes the evanescent wave of a totally internally reflecting laser beam to excite only those fluorescent molecules within one light wavelength or less of...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111781/ https://www.ncbi.nlm.nih.gov/pubmed/7014571 |
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collection | PubMed |
description | A technique for exciting fluorescence exclusively from regions of contact between cultured cells and the substrate is presented. The technique utilizes the evanescent wave of a totally internally reflecting laser beam to excite only those fluorescent molecules within one light wavelength or less of the substrate surface. Demonstrations of this technique are given for two types of cell cultures: rat primary myotubes with acetylcholine receptors labeled by fluorescent alpha- bungarotoxin and human skin fibroblasts labeled by a fluorescent lipid probe. Total internal reflection fluorescence examination of cells appears to have promising applications, including visualization of the membrane and underlying cytoplasmic structures at cell-substrate contacts, dramatic reduction of autofluorescence from debris and thick cells, mapping of membranes topography, and visualization of reversible bound fluorescent ligands at membrane receptors. |
format | Text |
id | pubmed-2111781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21117812008-05-01 Cell-substrate contacts illuminated by total internal reflection fluorescence J Cell Biol Articles A technique for exciting fluorescence exclusively from regions of contact between cultured cells and the substrate is presented. The technique utilizes the evanescent wave of a totally internally reflecting laser beam to excite only those fluorescent molecules within one light wavelength or less of the substrate surface. Demonstrations of this technique are given for two types of cell cultures: rat primary myotubes with acetylcholine receptors labeled by fluorescent alpha- bungarotoxin and human skin fibroblasts labeled by a fluorescent lipid probe. Total internal reflection fluorescence examination of cells appears to have promising applications, including visualization of the membrane and underlying cytoplasmic structures at cell-substrate contacts, dramatic reduction of autofluorescence from debris and thick cells, mapping of membranes topography, and visualization of reversible bound fluorescent ligands at membrane receptors. The Rockefeller University Press 1981-04-01 /pmc/articles/PMC2111781/ /pubmed/7014571 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Cell-substrate contacts illuminated by total internal reflection fluorescence |
title | Cell-substrate contacts illuminated by total internal reflection fluorescence |
title_full | Cell-substrate contacts illuminated by total internal reflection fluorescence |
title_fullStr | Cell-substrate contacts illuminated by total internal reflection fluorescence |
title_full_unstemmed | Cell-substrate contacts illuminated by total internal reflection fluorescence |
title_short | Cell-substrate contacts illuminated by total internal reflection fluorescence |
title_sort | cell-substrate contacts illuminated by total internal reflection fluorescence |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2111781/ https://www.ncbi.nlm.nih.gov/pubmed/7014571 |