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Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity

Monoblasts, promonocytes, and macrophages in in vitro cultures of murine bone marrow were studied ultrastructurally, with special attention to peroxidatic activity. Monoblasts show peroxidatic activity in the rough endoplasmic reticulum and nuclear envelope as well as in the granules. The presence o...

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Detalles Bibliográficos
Autores principales: Van Der Meer, JWM, Beelen, RHJ, Fluitsma, DM, Van Furth, R
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1979
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184748/
https://www.ncbi.nlm.nih.gov/pubmed/570211
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author Van Der Meer, JWM
Beelen, RHJ
Fluitsma, DM
Van Furth, R
author_facet Van Der Meer, JWM
Beelen, RHJ
Fluitsma, DM
Van Furth, R
author_sort Van Der Meer, JWM
collection PubMed
description Monoblasts, promonocytes, and macrophages in in vitro cultures of murine bone marrow were studied ultrastructurally, with special attention to peroxidatic activity. Monoblasts show peroxidatic activity in the rough endoplasmic reticulum and nuclear envelope as well as in the granules. The presence of peroxidatic activity in the Golgi apparatus could not be determined. Promonocytes have peroxidase-positive rough endoplasmic reticulum, Golgi apparatus, nuclear envelope, and granules, as previously reported. During culture, cells are formed with peroxidatic activity similar to that of monocytes or exudate macrophages (positive granules; negative Golgi apparatus, RER, and nuclear envelope); we call these cells early macrophages. In addition, transitional macrophages with both positive granules and positive RER, nuclear envelope, negative Golgi apparatus (as in exudate- resident macrophages in vivo), and mature macrophages with peroxidatic activity only in the RER and nuclear envelope (as in resident macrophages in vivo) were found. A considerable number of cells without detectable peroxidatic activity were also encountered. Our finding that macrophages with the peroxidatic pattern of monocytes (early macrophages), exudate-resident macrophages (transitional macrophages), and resident macrophages (mature macrophages), develop in vitro from proliferating precursor cells deriving from the bone marrow, demonstrates once again that resident macrophages in tissues originate from precursor cells in the bone marrow. Therefore, this conclusion can no longer be challenged on the basis of a cytochemical difference between monocytes and exudate macrophages on the one hand and resident macrophages on the other.
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spelling pubmed-21847482008-04-17 Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity Van Der Meer, JWM Beelen, RHJ Fluitsma, DM Van Furth, R J Exp Med Articles Monoblasts, promonocytes, and macrophages in in vitro cultures of murine bone marrow were studied ultrastructurally, with special attention to peroxidatic activity. Monoblasts show peroxidatic activity in the rough endoplasmic reticulum and nuclear envelope as well as in the granules. The presence of peroxidatic activity in the Golgi apparatus could not be determined. Promonocytes have peroxidase-positive rough endoplasmic reticulum, Golgi apparatus, nuclear envelope, and granules, as previously reported. During culture, cells are formed with peroxidatic activity similar to that of monocytes or exudate macrophages (positive granules; negative Golgi apparatus, RER, and nuclear envelope); we call these cells early macrophages. In addition, transitional macrophages with both positive granules and positive RER, nuclear envelope, negative Golgi apparatus (as in exudate- resident macrophages in vivo), and mature macrophages with peroxidatic activity only in the RER and nuclear envelope (as in resident macrophages in vivo) were found. A considerable number of cells without detectable peroxidatic activity were also encountered. Our finding that macrophages with the peroxidatic pattern of monocytes (early macrophages), exudate-resident macrophages (transitional macrophages), and resident macrophages (mature macrophages), develop in vitro from proliferating precursor cells deriving from the bone marrow, demonstrates once again that resident macrophages in tissues originate from precursor cells in the bone marrow. Therefore, this conclusion can no longer be challenged on the basis of a cytochemical difference between monocytes and exudate macrophages on the one hand and resident macrophages on the other. The Rockefeller University Press 1979-01-01 /pmc/articles/PMC2184748/ /pubmed/570211 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
Van Der Meer, JWM
Beelen, RHJ
Fluitsma, DM
Van Furth, R
Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title_full Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title_fullStr Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title_full_unstemmed Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title_short Ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. A study on peroxidatic activity
title_sort ultrastructure of mononuclear phagocytes developing in liquid bone marrow cultures. a study on peroxidatic activity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184748/
https://www.ncbi.nlm.nih.gov/pubmed/570211
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