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Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours.
The DNA-binding fluorescent dye Hoechst 33342 (H33342) has been used in a series of investigations of the vascular parameters of two murine tumours. This dye has been shown, to have a short half-life in the circulation (T1/2 less than 2 min), but is stably bound for at least 2 h after it enters cell...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1988
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246513/ https://www.ncbi.nlm.nih.gov/pubmed/3355762 |
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author | Smith, K. A. Hill, S. A. Begg, A. C. Denekamp, J. |
author_facet | Smith, K. A. Hill, S. A. Begg, A. C. Denekamp, J. |
author_sort | Smith, K. A. |
collection | PubMed |
description | The DNA-binding fluorescent dye Hoechst 33342 (H33342) has been used in a series of investigations of the vascular parameters of two murine tumours. This dye has been shown, to have a short half-life in the circulation (T1/2 less than 2 min), but is stably bound for at least 2 h after it enters cells. It can be used in morphometric studies on frozen sections to determine the effective vascular volume, the capillary fraction and the size distribution of blood vessels in each tumour. These latter two parameters cannot be deduced from the less labour intensive techniques using radioactive isotopes. The effective vascular volume perfused in 1 min by H33342 was compared with the volume perfused in 30 min with 51Cr labelled erythrocytes. Similar volumes were estimated with the two techniques in a murine carcinoma and in a sarcoma. Both techniques showed that the vascular volume decreased in larger tumours. The H33342 analysis of vessel size showed the decrease in capillary vessels in the carcinomas was even greater, falling from 70% in small tumours to 20% in larger tumours. The deteriorating vascular network in larger tumours is associated with an increasing fraction of necrotic tissue. Experiments in which the isotopes and dye were co-injected suggest that at 40 mgkg-1 the dye may rapidly lead to a partial shutdown of the tumour vascular bed. This is less marked with 20 mg kg-1. In spite of this effect there is in general a close correlation between the volumes perfused by labelled red blood cells and the fluorescent dye. IMAGES: |
format | Text |
id | pubmed-2246513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22465132009-09-10 Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. Smith, K. A. Hill, S. A. Begg, A. C. Denekamp, J. Br J Cancer Research Article The DNA-binding fluorescent dye Hoechst 33342 (H33342) has been used in a series of investigations of the vascular parameters of two murine tumours. This dye has been shown, to have a short half-life in the circulation (T1/2 less than 2 min), but is stably bound for at least 2 h after it enters cells. It can be used in morphometric studies on frozen sections to determine the effective vascular volume, the capillary fraction and the size distribution of blood vessels in each tumour. These latter two parameters cannot be deduced from the less labour intensive techniques using radioactive isotopes. The effective vascular volume perfused in 1 min by H33342 was compared with the volume perfused in 30 min with 51Cr labelled erythrocytes. Similar volumes were estimated with the two techniques in a murine carcinoma and in a sarcoma. Both techniques showed that the vascular volume decreased in larger tumours. The H33342 analysis of vessel size showed the decrease in capillary vessels in the carcinomas was even greater, falling from 70% in small tumours to 20% in larger tumours. The deteriorating vascular network in larger tumours is associated with an increasing fraction of necrotic tissue. Experiments in which the isotopes and dye were co-injected suggest that at 40 mgkg-1 the dye may rapidly lead to a partial shutdown of the tumour vascular bed. This is less marked with 20 mg kg-1. In spite of this effect there is in general a close correlation between the volumes perfused by labelled red blood cells and the fluorescent dye. IMAGES: Nature Publishing Group 1988-03 /pmc/articles/PMC2246513/ /pubmed/3355762 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 Smith, K. A. Hill, S. A. Begg, A. C. Denekamp, J. Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title | Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title_full | Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title_fullStr | Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title_full_unstemmed | Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title_short | Validation of the fluorescent dye Hoechst 33342 as a vascular space marker in tumours. |
title_sort | validation of the fluorescent dye hoechst 33342 as a vascular space marker in tumours. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246513/ https://www.ncbi.nlm.nih.gov/pubmed/3355762 |
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