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Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo
We have investigated the ability of recombinant TNF (mouse and human) to produce acute inflammatory lesions in an established experimental model of inflammation. Upon intradermal injection in rabbit skin, TNF, in amounts as low as 3 x 10(-14) mol/site, was found to be very potent at inducing local n...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189351/ https://www.ncbi.nlm.nih.gov/pubmed/2659725 |
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collection | PubMed |
description | We have investigated the ability of recombinant TNF (mouse and human) to produce acute inflammatory lesions in an established experimental model of inflammation. Upon intradermal injection in rabbit skin, TNF, in amounts as low as 3 x 10(-14) mol/site, was found to be very potent at inducing local neutrophil accumulation and neutrophil-dependent oedema formation, thereby fulfilling two important criteria to be considered as an inflammatory mediator. Our findings further indicate that the pro-inflammatory properties of TNF are probably more related to its immediate stimulatory effects on neutrophils rather than to its slow (protein biosynthesis-dependent effects on endothelial cells. Our data thus show that very low amounts of mouse and human recombinant TNF can initiate an acute inflammatory reaction in vivo in rabbit skin and that TNF is able to evoke two of the four cardinal signs of inflammation. |
format | Text |
id | pubmed-2189351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21893512008-04-17 Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo J Exp Med Articles We have investigated the ability of recombinant TNF (mouse and human) to produce acute inflammatory lesions in an established experimental model of inflammation. Upon intradermal injection in rabbit skin, TNF, in amounts as low as 3 x 10(-14) mol/site, was found to be very potent at inducing local neutrophil accumulation and neutrophil-dependent oedema formation, thereby fulfilling two important criteria to be considered as an inflammatory mediator. Our findings further indicate that the pro-inflammatory properties of TNF are probably more related to its immediate stimulatory effects on neutrophils rather than to its slow (protein biosynthesis-dependent effects on endothelial cells. Our data thus show that very low amounts of mouse and human recombinant TNF can initiate an acute inflammatory reaction in vivo in rabbit skin and that TNF is able to evoke two of the four cardinal signs of inflammation. The Rockefeller University Press 1989-06-01 /pmc/articles/PMC2189351/ /pubmed/2659725 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 Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title | Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title_full | Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title_fullStr | Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title_full_unstemmed | Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title_short | Inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
title_sort | inflammatory properties of recombinant tumor necrosis factor in rabbit skin in vivo |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189351/ https://www.ncbi.nlm.nih.gov/pubmed/2659725 |