Cargando…

THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES

The contents of selected hydrolytic enzymes of oil-induced peritoneal, normal alveolar, and BCG-induced alveolar macrophages have been studied. On a per cell or nitrogen basis the normal alveolar cells contained considerably more acid phosphatase, cathepsin, acid ribonuclease, lysozyme, and lipase t...

Descripción completa

Detalles Bibliográficos
Autores principales: Cohn, Zanvil A., Wiener, Edith
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1963
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137687/
https://www.ncbi.nlm.nih.gov/pubmed/14112277
_version_ 1782143390288183296
author Cohn, Zanvil A.
Wiener, Edith
author_facet Cohn, Zanvil A.
Wiener, Edith
author_sort Cohn, Zanvil A.
collection PubMed
description The contents of selected hydrolytic enzymes of oil-induced peritoneal, normal alveolar, and BCG-induced alveolar macrophages have been studied. On a per cell or nitrogen basis the normal alveolar cells contained considerably more acid phosphatase, cathepsin, acid ribonuclease, lysozyme, and lipase than peritoneal cells. The BCG-induced alveolar macrophage exhibited increased levels of acid phosphatase, lysozyme, and lipase as compared to alveolar macrophages from unstimulated rabbits. The morphological differences between these cells was discussed and electron micrographs of the BCG-induced macrophage presented. Fractionation of the BCG-induced macrophage by differential centrifugation showed that 60 to 80 per cent of the total cell content of acid phosphatase, cathepsin, beta glucuronidase, acid ribonuclease, acid deoxyribonuclease, aryl sulfatase, lysozyme, and lipase were localized in a postnuclear fraction which sedimented at 15,000 g. This fraction also contained the majority of the mitochondria as evidenced by its content of cytochrome oxidase. Non-specific esterase was not localized to this fraction. A separation of the hydrolase-containing particles and mitochondria was achieved by isopycnic sucrose gradient centrifugation. Under the conditions employed, the mitochondria distributed at densities of 1.19 to 1.20, whereas the hydrolase particles sedimented to a density of 1.26 to 1.27. Each of the hydrolases including acid phosphatase, beta glucuronidase, cathepsin, lysozyme, and acid ribonuclease exhibited maximum activities in the same gradient fraction. The isolated granules exhibited enzymatic latency, and activation could be achieved by cycles of freezing and thawing or surface active agents. The majority of each of the hydrolytic enzymes could be liberated in a non-particulate form by mechanical trauma. Macrophages which had been stained supravitally with neutral red were fractionated by differential and gradient centrifugation. More than 70 per cent of the dye could be recovered in the particulate hydrolase fraction. The isolated, stained granules resembled those seen in the intact cell.
format Text
id pubmed-2137687
institution National Center for Biotechnology Information
language English
publishDate 1963
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21376872008-04-17 THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES Cohn, Zanvil A. Wiener, Edith J Exp Med Article The contents of selected hydrolytic enzymes of oil-induced peritoneal, normal alveolar, and BCG-induced alveolar macrophages have been studied. On a per cell or nitrogen basis the normal alveolar cells contained considerably more acid phosphatase, cathepsin, acid ribonuclease, lysozyme, and lipase than peritoneal cells. The BCG-induced alveolar macrophage exhibited increased levels of acid phosphatase, lysozyme, and lipase as compared to alveolar macrophages from unstimulated rabbits. The morphological differences between these cells was discussed and electron micrographs of the BCG-induced macrophage presented. Fractionation of the BCG-induced macrophage by differential centrifugation showed that 60 to 80 per cent of the total cell content of acid phosphatase, cathepsin, beta glucuronidase, acid ribonuclease, acid deoxyribonuclease, aryl sulfatase, lysozyme, and lipase were localized in a postnuclear fraction which sedimented at 15,000 g. This fraction also contained the majority of the mitochondria as evidenced by its content of cytochrome oxidase. Non-specific esterase was not localized to this fraction. A separation of the hydrolase-containing particles and mitochondria was achieved by isopycnic sucrose gradient centrifugation. Under the conditions employed, the mitochondria distributed at densities of 1.19 to 1.20, whereas the hydrolase particles sedimented to a density of 1.26 to 1.27. Each of the hydrolases including acid phosphatase, beta glucuronidase, cathepsin, lysozyme, and acid ribonuclease exhibited maximum activities in the same gradient fraction. The isolated granules exhibited enzymatic latency, and activation could be achieved by cycles of freezing and thawing or surface active agents. The majority of each of the hydrolytic enzymes could be liberated in a non-particulate form by mechanical trauma. Macrophages which had been stained supravitally with neutral red were fractionated by differential and gradient centrifugation. More than 70 per cent of the dye could be recovered in the particulate hydrolase fraction. The isolated, stained granules resembled those seen in the intact cell. The Rockefeller University Press 1963-11-30 /pmc/articles/PMC2137687/ /pubmed/14112277 Text en Copyright © 1963, by The Rockefeller Institute 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
Cohn, Zanvil A.
Wiener, Edith
THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title_full THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title_fullStr THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title_full_unstemmed THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title_short THE PARTICULATE HYDROLASES OF MACROPHAGES : I. COMPARATIVE ENZYMOLOGY, ISOLATION, AND PROPERTIES
title_sort particulate hydrolases of macrophages : i. comparative enzymology, isolation, and properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137687/
https://www.ncbi.nlm.nih.gov/pubmed/14112277
work_keys_str_mv AT cohnzanvila theparticulatehydrolasesofmacrophagesicomparativeenzymologyisolationandproperties
AT wieneredith theparticulatehydrolasesofmacrophagesicomparativeenzymologyisolationandproperties
AT cohnzanvila particulatehydrolasesofmacrophagesicomparativeenzymologyisolationandproperties
AT wieneredith particulatehydrolasesofmacrophagesicomparativeenzymologyisolationandproperties