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STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN
Histochemical and ultrastructural studies demonstrate that keratohyalin can be mobilized from fresh specimens of cattle hoof epidermis by 1.0 M potassium phosphate buffer (pH 7.0). Macroaggregates with histochemical characteristics identical to those of in situ keratohyalin granules (staining by Har...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1971
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108338/ https://www.ncbi.nlm.nih.gov/pubmed/19866768 |
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author | Ugel, Arthur R. |
author_facet | Ugel, Arthur R. |
author_sort | Ugel, Arthur R. |
collection | PubMed |
description | Histochemical and ultrastructural studies demonstrate that keratohyalin can be mobilized from fresh specimens of cattle hoof epidermis by 1.0 M potassium phosphate buffer (pH 7.0). Macroaggregates with histochemical characteristics identical to those of in situ keratohyalin granules (staining by Harris' hematoxylin, Congo red, diazotized sulfanilic acid, sodium alizarin sulfonate, toluidine blue, methyl green-pyronin, and acridine orange) and with similar morphological characteristics at the ultrastructural level are formed upon dialyzing the extracted keratohyalin against distilled water. Staining by basic dyes (toluidine blue, methyl green-pyronin, and acridine orange) is abolished by treating either in situ keratohyalin granules or isolated macroaggregates with ribonuclease. Electrophoresis of isolated macroaggregates on polyacrylamide gels in the presence of sodium decylsulfate results in the fractionation of a 13 member oligomeric series of ribonucleoproteins and two non-homologous species of ribonucleoproteins. The oligomeric series can be purified by isolating "stacked" oligomers on low concentration (3%) polyacrylamide gels. Fractionated oligomers on polyacrylamide gels and aggregates formed from purified ribonucleoproteins demonstrate histochemical characteristics identical to those of in situ keratohyalin granules. Aggregates formed from denatured ribonucleoproteins are highly disordered and are markedly different from in situ keratohyalin granules or nondenatured isolated macroaggregates at the ultrastructural level, possibly due to irreversible denaturation of the oligomers by sodium decylsulfate. |
format | Text |
id | pubmed-2108338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1971 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21083382008-05-01 STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN Ugel, Arthur R. J Cell Biol Article Histochemical and ultrastructural studies demonstrate that keratohyalin can be mobilized from fresh specimens of cattle hoof epidermis by 1.0 M potassium phosphate buffer (pH 7.0). Macroaggregates with histochemical characteristics identical to those of in situ keratohyalin granules (staining by Harris' hematoxylin, Congo red, diazotized sulfanilic acid, sodium alizarin sulfonate, toluidine blue, methyl green-pyronin, and acridine orange) and with similar morphological characteristics at the ultrastructural level are formed upon dialyzing the extracted keratohyalin against distilled water. Staining by basic dyes (toluidine blue, methyl green-pyronin, and acridine orange) is abolished by treating either in situ keratohyalin granules or isolated macroaggregates with ribonuclease. Electrophoresis of isolated macroaggregates on polyacrylamide gels in the presence of sodium decylsulfate results in the fractionation of a 13 member oligomeric series of ribonucleoproteins and two non-homologous species of ribonucleoproteins. The oligomeric series can be purified by isolating "stacked" oligomers on low concentration (3%) polyacrylamide gels. Fractionated oligomers on polyacrylamide gels and aggregates formed from purified ribonucleoproteins demonstrate histochemical characteristics identical to those of in situ keratohyalin granules. Aggregates formed from denatured ribonucleoproteins are highly disordered and are markedly different from in situ keratohyalin granules or nondenatured isolated macroaggregates at the ultrastructural level, possibly due to irreversible denaturation of the oligomers by sodium decylsulfate. The Rockefeller University Press 1971-05-01 /pmc/articles/PMC2108338/ /pubmed/19866768 Text en Copyright © 1971 by The Rockefeller University Press 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 | Article Ugel, Arthur R. STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title | STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title_full | STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title_fullStr | STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title_full_unstemmed | STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title_short | STUDIES ON ISOLATED AGGREGATING OLIGORIBONUCLEOPROTEINS OF THE EPIDERMIS WITH HISTOCHEMICAL AND MORPHOLOGICAL CHARACTERISTICS OF KERATOHYALIN |
title_sort | studies on isolated aggregating oligoribonucleoproteins of the epidermis with histochemical and morphological characteristics of keratohyalin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108338/ https://www.ncbi.nlm.nih.gov/pubmed/19866768 |
work_keys_str_mv | AT ugelarthurr studiesonisolatedaggregatingoligoribonucleoproteinsoftheepidermiswithhistochemicalandmorphologicalcharacteristicsofkeratohyalin |