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Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.

3M-KCl extracts of the hepatoma D23 contain antigens that inhibit the complement-dependent cytotoxicity for D23 hepatoma cells of serum from D23 tumour-bearing rats (D23 TBS). Inhibition was not due to a general anticomplementary activity of the extracts. Although a minor part (25%) of the protein o...

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Autores principales: Lando, P., Berzins, K., Gabriel, J., Larsson, P., Perlmann, P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010806/
https://www.ncbi.nlm.nih.gov/pubmed/7295508
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author Lando, P.
Berzins, K.
Gabriel, J.
Larsson, P.
Perlmann, P.
author_facet Lando, P.
Berzins, K.
Gabriel, J.
Larsson, P.
Perlmann, P.
author_sort Lando, P.
collection PubMed
description 3M-KCl extracts of the hepatoma D23 contain antigens that inhibit the complement-dependent cytotoxicity for D23 hepatoma cells of serum from D23 tumour-bearing rats (D23 TBS). Inhibition was not due to a general anticomplementary activity of the extracts. Although a minor part (25%) of the protein of D23-KCl extract was insoluble in PBS, this part contained most of the inhibitory activity. Fractionation of the PBS-soluble material of the extract on Concanavalin A-Sepharose showed that the inhibitory activity did not bind to the lectin. Analysis of D23-KCl extracts on a Sepharose CL-4B column showed that the antigens involved in the cytotoxicity were heterogeneously distributed in the high-mol. wt region (greater than 200,000). Precipitation with 10% trichloroacetic acid (TCA) of D23 KCl extracts revealed that most of the antigenicity was insoluble in TCA. Heating of D23 KCl extracts at 100 degrees C did not affect the antigenicity. Enzyme treatment of D23 extra nuclear membranes (D23 ENP) revealed that the inhibitory activity was not sensitive to proteolytic digestion, while treatment with phospholipase A2, C or D abrogated partly the inhibitory activity. The lipid nature of the antigenicity was indicated by its solubility in organic solvents as chloroform or n-butanol. IMAGES:
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spelling pubmed-20108062009-09-10 Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats. Lando, P. Berzins, K. Gabriel, J. Larsson, P. Perlmann, P. Br J Cancer Research Article 3M-KCl extracts of the hepatoma D23 contain antigens that inhibit the complement-dependent cytotoxicity for D23 hepatoma cells of serum from D23 tumour-bearing rats (D23 TBS). Inhibition was not due to a general anticomplementary activity of the extracts. Although a minor part (25%) of the protein of D23-KCl extract was insoluble in PBS, this part contained most of the inhibitory activity. Fractionation of the PBS-soluble material of the extract on Concanavalin A-Sepharose showed that the inhibitory activity did not bind to the lectin. Analysis of D23-KCl extracts on a Sepharose CL-4B column showed that the antigens involved in the cytotoxicity were heterogeneously distributed in the high-mol. wt region (greater than 200,000). Precipitation with 10% trichloroacetic acid (TCA) of D23 KCl extracts revealed that most of the antigenicity was insoluble in TCA. Heating of D23 KCl extracts at 100 degrees C did not affect the antigenicity. Enzyme treatment of D23 extra nuclear membranes (D23 ENP) revealed that the inhibitory activity was not sensitive to proteolytic digestion, while treatment with phospholipase A2, C or D abrogated partly the inhibitory activity. The lipid nature of the antigenicity was indicated by its solubility in organic solvents as chloroform or n-butanol. IMAGES: Nature Publishing Group 1981-10 /pmc/articles/PMC2010806/ /pubmed/7295508 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
Lando, P.
Berzins, K.
Gabriel, J.
Larsson, P.
Perlmann, P.
Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title_full Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title_fullStr Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title_full_unstemmed Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title_short Tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
title_sort tumour-associated antigens reacting with cytotoxic antibodies in serum of hepatoma-bearing rats.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010806/
https://www.ncbi.nlm.nih.gov/pubmed/7295508
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