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Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties.
Sera from rabbits injected with BCG and then with endotoxin contain a factor (tumour-necrosis factor TNF) which, even at high dilutions, is cytotoxic in vitro for mouse L cells and some other cell lines. Using a 51Cr-release assay, cytotoxicity was detected as early as 7-8 h after addition of TNF se...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1978
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009711/ https://www.ncbi.nlm.nih.gov/pubmed/698046 |
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author | Matthews, N. Watkins, J. F. |
author_facet | Matthews, N. Watkins, J. F. |
author_sort | Matthews, N. |
collection | PubMed |
description | Sera from rabbits injected with BCG and then with endotoxin contain a factor (tumour-necrosis factor TNF) which, even at high dilutions, is cytotoxic in vitro for mouse L cells and some other cell lines. Using a 51Cr-release assay, cytotoxicity was detected as early as 7-8 h after addition of TNF serum to L cells and cell death was evident microscopically by 24 h. TNF was cytotoxic at 37 degrees C but not at 21 degrees C or 4 degrees C, and acted on both dividing and non-dividing cells. The antimetabolites sodium azide and dinitrophenol partially protected L cells from TNF, suggesting that actively metabolizing cells are the most sensitive. Treatment of L cells with trypsin did not delay cytotoxicity nor was cytotoxicity inhibited in the presence of various saccharide derivatives of cell-surface glycoproteins. Rabbit TNF was remarkably stable with a mol. wt. of 40-50,000. It was eluted with the more acidic serum proteins on ion-exchange chromatography, but precipitated in 50%-saturated ammonium sulphate. Sensitivity to TNF could not be correlated with tumourigenicity of several animal and human lines tested nor with the production of C-type viruses. IMAGES: |
format | Text |
id | pubmed-2009711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1978 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20097112009-09-10 Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. Matthews, N. Watkins, J. F. Br J Cancer Research Article Sera from rabbits injected with BCG and then with endotoxin contain a factor (tumour-necrosis factor TNF) which, even at high dilutions, is cytotoxic in vitro for mouse L cells and some other cell lines. Using a 51Cr-release assay, cytotoxicity was detected as early as 7-8 h after addition of TNF serum to L cells and cell death was evident microscopically by 24 h. TNF was cytotoxic at 37 degrees C but not at 21 degrees C or 4 degrees C, and acted on both dividing and non-dividing cells. The antimetabolites sodium azide and dinitrophenol partially protected L cells from TNF, suggesting that actively metabolizing cells are the most sensitive. Treatment of L cells with trypsin did not delay cytotoxicity nor was cytotoxicity inhibited in the presence of various saccharide derivatives of cell-surface glycoproteins. Rabbit TNF was remarkably stable with a mol. wt. of 40-50,000. It was eluted with the more acidic serum proteins on ion-exchange chromatography, but precipitated in 50%-saturated ammonium sulphate. Sensitivity to TNF could not be correlated with tumourigenicity of several animal and human lines tested nor with the production of C-type viruses. IMAGES: Nature Publishing Group 1978-08 /pmc/articles/PMC2009711/ /pubmed/698046 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Matthews, N. Watkins, J. F. Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title | Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title_full | Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title_fullStr | Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title_full_unstemmed | Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title_short | Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. |
title_sort | tumour-necrosis factor from the rabbit. i. mode of action, specificity and physicochemical properties. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009711/ https://www.ncbi.nlm.nih.gov/pubmed/698046 |
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