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SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES

Rabbit ieukocytes from peritoneal exudates and from blood were stimulated to form leukocyte pyrogen in the presence of radiolabeled amino acids. The stimuli used were endotoxin, phagocytosis, and tuberculin. The crude leukocyte pyrogen samples were purified; pyrogen from exudate cells was rendered h...

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Detalles Bibliográficos
Autores principales: Moore, Douglas M., Murphy, Patrick A., Chesney, P. Joan, Wood, W. B.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1973
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139241/
https://www.ncbi.nlm.nih.gov/pubmed/4573840
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author Moore, Douglas M.
Murphy, Patrick A.
Chesney, P. Joan
Wood, W. B.
author_facet Moore, Douglas M.
Murphy, Patrick A.
Chesney, P. Joan
Wood, W. B.
author_sort Moore, Douglas M.
collection PubMed
description Rabbit ieukocytes from peritoneal exudates and from blood were stimulated to form leukocyte pyrogen in the presence of radiolabeled amino acids. The stimuli used were endotoxin, phagocytosis, and tuberculin. The crude leukocyte pyrogen samples were purified; pyrogen from exudate cells was rendered homogeneous; pyrogen from blood cells was still contaminated with other proteins. All the purified pyrogens were radioactive; and for all it was shown that radioactivity and pyrogenic activity coincided on electrophoresis at pH 3.5 and pH 9 in acrylamide and on isoelectric focusing in acrylamide. Furthermore, pyrogens obtained from exudate cells stimulated in different ways, or from blood cells and exudate cells stimulated with endotoxin, appeared to be identical. These results suggest that leukocyte pyrogen was synthesized de novo from amino acid precursors and that leukocytes made the same pyrogen whatever the stimulus used to activate them.
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spelling pubmed-21392412008-04-17 SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES Moore, Douglas M. Murphy, Patrick A. Chesney, P. Joan Wood, W. B. J Exp Med Article Rabbit ieukocytes from peritoneal exudates and from blood were stimulated to form leukocyte pyrogen in the presence of radiolabeled amino acids. The stimuli used were endotoxin, phagocytosis, and tuberculin. The crude leukocyte pyrogen samples were purified; pyrogen from exudate cells was rendered homogeneous; pyrogen from blood cells was still contaminated with other proteins. All the purified pyrogens were radioactive; and for all it was shown that radioactivity and pyrogenic activity coincided on electrophoresis at pH 3.5 and pH 9 in acrylamide and on isoelectric focusing in acrylamide. Furthermore, pyrogens obtained from exudate cells stimulated in different ways, or from blood cells and exudate cells stimulated with endotoxin, appeared to be identical. These results suggest that leukocyte pyrogen was synthesized de novo from amino acid precursors and that leukocytes made the same pyrogen whatever the stimulus used to activate them. The Rockefeller University Press 1973-05-01 /pmc/articles/PMC2139241/ /pubmed/4573840 Text en Copyright © 1973 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
Moore, Douglas M.
Murphy, Patrick A.
Chesney, P. Joan
Wood, W. B.
SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title_full SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title_fullStr SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title_full_unstemmed SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title_short SYNTHESIS OF ENDOGENOUS PYROGEN BY RABBIT LEUKOCYTES
title_sort synthesis of endogenous pyrogen by rabbit leukocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139241/
https://www.ncbi.nlm.nih.gov/pubmed/4573840
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