Cargando…

Expression of c-fos protooncogene in normal human peripheral blood granulocytes

We have investigated by Northern blot analysis the expression of c-fos protooncogene in human peripheral blood polymorphonuclear leukocytes (PMN). Freshly isolated PMN, unlike highly purified circulating lymphoid cells, showed high levels of c-fos transcripts. Appreciable c- fos mRNA was detected in...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188587/
https://www.ncbi.nlm.nih.gov/pubmed/3104528
_version_ 1782146443418533888
collection PubMed
description We have investigated by Northern blot analysis the expression of c-fos protooncogene in human peripheral blood polymorphonuclear leukocytes (PMN). Freshly isolated PMN, unlike highly purified circulating lymphoid cells, showed high levels of c-fos transcripts. Appreciable c- fos mRNA was detected in monocytes, but in lesser amounts compared with PMN. Upon exposure to a series of agents that functionally stimulate granulocytes (PMA, inactivated streptococci, TNF, granulocyte and granulocyte/macrophage colony-stimulating factor), a considerable increase in c-fos transcripts was detected. Expression of c-fos in PMN was superinduced by exposure to cycloheximide. These data indicate that the myelomonocytic differentiation pathway c-fos expression is not peculiar to monocytes/macrophages and that PMN may represent a suitable system with which to investigate the link between protooncogene expression and functional activation.
format Text
id pubmed-2188587
institution National Center for Biotechnology Information
language English
publishDate 1987
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21885872008-04-17 Expression of c-fos protooncogene in normal human peripheral blood granulocytes J Exp Med Articles We have investigated by Northern blot analysis the expression of c-fos protooncogene in human peripheral blood polymorphonuclear leukocytes (PMN). Freshly isolated PMN, unlike highly purified circulating lymphoid cells, showed high levels of c-fos transcripts. Appreciable c- fos mRNA was detected in monocytes, but in lesser amounts compared with PMN. Upon exposure to a series of agents that functionally stimulate granulocytes (PMA, inactivated streptococci, TNF, granulocyte and granulocyte/macrophage colony-stimulating factor), a considerable increase in c-fos transcripts was detected. Expression of c-fos in PMN was superinduced by exposure to cycloheximide. These data indicate that the myelomonocytic differentiation pathway c-fos expression is not peculiar to monocytes/macrophages and that PMN may represent a suitable system with which to investigate the link between protooncogene expression and functional activation. The Rockefeller University Press 1987-04-01 /pmc/articles/PMC2188587/ /pubmed/3104528 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
Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title_full Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title_fullStr Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title_full_unstemmed Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title_short Expression of c-fos protooncogene in normal human peripheral blood granulocytes
title_sort expression of c-fos protooncogene in normal human peripheral blood granulocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188587/
https://www.ncbi.nlm.nih.gov/pubmed/3104528