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Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.

Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans (PGs) was observed in 70 tumour tissues, using monoclonal antibodies 9A-2 and 3B-3 raised against core molecules obtained from chondroitin sulphate PG by chondroitinase ABC-treatment. They recognize a stub o...

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Autores principales: Fukatsu, T., Sobue, M., Nagasaka, T., Ohiwa, N., Fukata, S., Nakashima, N., Takeuchi, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246697/
https://www.ncbi.nlm.nih.gov/pubmed/3348950
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author Fukatsu, T.
Sobue, M.
Nagasaka, T.
Ohiwa, N.
Fukata, S.
Nakashima, N.
Takeuchi, J.
author_facet Fukatsu, T.
Sobue, M.
Nagasaka, T.
Ohiwa, N.
Fukata, S.
Nakashima, N.
Takeuchi, J.
author_sort Fukatsu, T.
collection PubMed
description Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans (PGs) was observed in 70 tumour tissues, using monoclonal antibodies 9A-2 and 3B-3 raised against core molecules obtained from chondroitin sulphate PG by chondroitinase ABC-treatment. They recognize a stub of delta Di-4S and delta Di-6S binding to core protein via a linkage tetrasaccharide, respectively. The antibody 6B6 raised against dermatan sulphate PG obtained from an ovarian fibroma capsule in our laboratory was also used. The interstitial fibrous elements, so-called 'specific stroma' within the cancer cell nests contained chondroitin 4-sulphate PG as revealed with 9A-2, whereas the surrounding connective tissue and the preexisting fibrous connective tissue involved in the tumour growth consisted of dermatan sulphate PG with a considerable amount of chondroitin 4-sulphate PG. Chondroitin 6-sulphate PG as revealed with 3B-3 was located in the connective tissue proliferating from blood vessels and muscle tissue in association with the invasive growth of tumour cells. Chondroitin 6-sulphate PG was also observed in the basement membrane components of some tumours. In non-epithelial tumours (fibrogenic, chondrogenic, osteogenic and neurogenic tumours), chondroitin 4-sulphate was in fibrous portions. When collagenization and hyalinization progressed, dermatan sulphate PG was observed to increase in quantity. IMAGES:
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spelling pubmed-22466972009-09-10 Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues. Fukatsu, T. Sobue, M. Nagasaka, T. Ohiwa, N. Fukata, S. Nakashima, N. Takeuchi, J. Br J Cancer Research Article Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans (PGs) was observed in 70 tumour tissues, using monoclonal antibodies 9A-2 and 3B-3 raised against core molecules obtained from chondroitin sulphate PG by chondroitinase ABC-treatment. They recognize a stub of delta Di-4S and delta Di-6S binding to core protein via a linkage tetrasaccharide, respectively. The antibody 6B6 raised against dermatan sulphate PG obtained from an ovarian fibroma capsule in our laboratory was also used. The interstitial fibrous elements, so-called 'specific stroma' within the cancer cell nests contained chondroitin 4-sulphate PG as revealed with 9A-2, whereas the surrounding connective tissue and the preexisting fibrous connective tissue involved in the tumour growth consisted of dermatan sulphate PG with a considerable amount of chondroitin 4-sulphate PG. Chondroitin 6-sulphate PG as revealed with 3B-3 was located in the connective tissue proliferating from blood vessels and muscle tissue in association with the invasive growth of tumour cells. Chondroitin 6-sulphate PG was also observed in the basement membrane components of some tumours. In non-epithelial tumours (fibrogenic, chondrogenic, osteogenic and neurogenic tumours), chondroitin 4-sulphate was in fibrous portions. When collagenization and hyalinization progressed, dermatan sulphate PG was observed to increase in quantity. IMAGES: Nature Publishing Group 1988-01 /pmc/articles/PMC2246697/ /pubmed/3348950 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
Fukatsu, T.
Sobue, M.
Nagasaka, T.
Ohiwa, N.
Fukata, S.
Nakashima, N.
Takeuchi, J.
Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title_full Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title_fullStr Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title_full_unstemmed Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title_short Immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
title_sort immunohistochemical localization of chondroitin sulphate and dermatan sulphate proteoglycans in tumour tissues.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246697/
https://www.ncbi.nlm.nih.gov/pubmed/3348950
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