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LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE
A method has been described for the detection of streptococcal antigens in tissues using the indirect immunofluorescent technique. This method has been applied to the histologic distribution in the mouse of M protein of types 1, 5, 12, and 19. Histologic localization of these M proteins was similar,...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1958
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136689/ https://www.ncbi.nlm.nih.gov/pubmed/13513904 |
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author | Kaplan, Melvin H. |
author_facet | Kaplan, Melvin H. |
author_sort | Kaplan, Melvin H. |
collection | PubMed |
description | A method has been described for the detection of streptococcal antigens in tissues using the indirect immunofluorescent technique. This method has been applied to the histologic distribution in the mouse of M protein of types 1, 5, 12, and 19. Histologic localization of these M proteins was similar, and their rates of disappearance from the tissues were comparable. The major sites of deposition were the endocardium and adjacent subendocardium of the heart, alveolar walls of the lung, glomerular tufts of the kidney, and reticulo-endothelial cells of liver, spleen, lymph nodes, and adrenal gland. M protein was distributed in considerably lesser concentration in capillary endothelium and connective tissue sites in myocardium, kidney, skin, and gastrointestinal tract. Traces were also present in adrenal cortical cells. It was observed only rarely in cell nuclei. After injection of 0.5 mg. M protein fraction, the concentration of antigen diminished to undetectable levels in all organ sites by 4 days, except in the renal glomerulus, where traces were visible at 8 days. In mice injected with streptococcal culture intraperitoneally, M protein was detected at sites of focal abscesses in liver and spleen, and on the serous surfaces of these organs. The histologic distribution of M protein is compared with that described previously for pneumococcal polysaccharide and animal protein. Differences in the extent of distribution and in the characteristics of antigen deposition are pointed out. |
format | Text |
id | pubmed-2136689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1958 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21366892008-04-17 LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE Kaplan, Melvin H. J Exp Med Article A method has been described for the detection of streptococcal antigens in tissues using the indirect immunofluorescent technique. This method has been applied to the histologic distribution in the mouse of M protein of types 1, 5, 12, and 19. Histologic localization of these M proteins was similar, and their rates of disappearance from the tissues were comparable. The major sites of deposition were the endocardium and adjacent subendocardium of the heart, alveolar walls of the lung, glomerular tufts of the kidney, and reticulo-endothelial cells of liver, spleen, lymph nodes, and adrenal gland. M protein was distributed in considerably lesser concentration in capillary endothelium and connective tissue sites in myocardium, kidney, skin, and gastrointestinal tract. Traces were also present in adrenal cortical cells. It was observed only rarely in cell nuclei. After injection of 0.5 mg. M protein fraction, the concentration of antigen diminished to undetectable levels in all organ sites by 4 days, except in the renal glomerulus, where traces were visible at 8 days. In mice injected with streptococcal culture intraperitoneally, M protein was detected at sites of focal abscesses in liver and spleen, and on the serous surfaces of these organs. The histologic distribution of M protein is compared with that described previously for pneumococcal polysaccharide and animal protein. Differences in the extent of distribution and in the characteristics of antigen deposition are pointed out. The Rockefeller University Press 1958-02-28 /pmc/articles/PMC2136689/ /pubmed/13513904 Text en Copyright © Copyright, 1958, by The Rockefeller Institute for Medical Research New York 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 Kaplan, Melvin H. LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title | LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title_full | LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title_fullStr | LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title_full_unstemmed | LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title_short | LOCALIZATION OF STREPTOCOCCAL ANTIGENS IN TISSUES : I. HISTOLOGIC DISTRIBUTION AND PERSISTENCE OF M PROTEIN, TYPES 1, 5, 12, AND 19 IN THE TISSUES OF THE MOUSE |
title_sort | localization of streptococcal antigens in tissues : i. histologic distribution and persistence of m protein, types 1, 5, 12, and 19 in the tissues of the mouse |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2136689/ https://www.ncbi.nlm.nih.gov/pubmed/13513904 |
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