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Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth.
As it has been suggested that an autocrine mechanism may control tumour cell growth, in this work cells from a spontaneous murine T lymphocyte leukaemia (LB) expressing the interleukin-2 receptor (IL-2R) (CD25) were evaluated in vitro for IL-2-mediated autocrine growth. Cells grew readily in culture...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222760/ https://www.ncbi.nlm.nih.gov/pubmed/9083328 |
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author | Waldner, C. I. Mongini, C. Alvarez, E. Sánchez Lockhart, M. Gravisaco, M. J. Hajos, S. E. |
author_facet | Waldner, C. I. Mongini, C. Alvarez, E. Sánchez Lockhart, M. Gravisaco, M. J. Hajos, S. E. |
author_sort | Waldner, C. I. |
collection | PubMed |
description | As it has been suggested that an autocrine mechanism may control tumour cell growth, in this work cells from a spontaneous murine T lymphocyte leukaemia (LB) expressing the interleukin-2 receptor (IL-2R) (CD25) were evaluated in vitro for IL-2-mediated autocrine growth. Cells grew readily in culture and proliferation was enhanced by the addition of recombinant IL-2 but inhibited by monoclonal antibodies against either IL-2 or IL-2 receptor, in the absence of exogenous IL-2. Cyclosporin A also inhibited LB cell growth. However, when exogenous IL-2 was added together with cyclosporin A, cell proliferation proved similar to controls. Using reverse transcription polymerase chain reaction (PCR), mRNA for IL-2 was found to be present in tumour cells. Our findings support the hypothesis that LB tumour cell proliferation is mediated by an autocrine pathway involving endogenous IL-2 generation, despite the fact that these cells are not dependent on exogenous IL-2 to grow in culture. IMAGES: |
format | Text |
id | pubmed-2222760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22227602009-09-10 Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. Waldner, C. I. Mongini, C. Alvarez, E. Sánchez Lockhart, M. Gravisaco, M. J. Hajos, S. E. Br J Cancer Research Article As it has been suggested that an autocrine mechanism may control tumour cell growth, in this work cells from a spontaneous murine T lymphocyte leukaemia (LB) expressing the interleukin-2 receptor (IL-2R) (CD25) were evaluated in vitro for IL-2-mediated autocrine growth. Cells grew readily in culture and proliferation was enhanced by the addition of recombinant IL-2 but inhibited by monoclonal antibodies against either IL-2 or IL-2 receptor, in the absence of exogenous IL-2. Cyclosporin A also inhibited LB cell growth. However, when exogenous IL-2 was added together with cyclosporin A, cell proliferation proved similar to controls. Using reverse transcription polymerase chain reaction (PCR), mRNA for IL-2 was found to be present in tumour cells. Our findings support the hypothesis that LB tumour cell proliferation is mediated by an autocrine pathway involving endogenous IL-2 generation, despite the fact that these cells are not dependent on exogenous IL-2 to grow in culture. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2222760/ /pubmed/9083328 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 Waldner, C. I. Mongini, C. Alvarez, E. Sánchez Lockhart, M. Gravisaco, M. J. Hajos, S. E. Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title | Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title_full | Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title_fullStr | Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title_full_unstemmed | Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title_short | Interleukin 2 exerts autocrine stimulation on murine T-cell leukaemia growth. |
title_sort | interleukin 2 exerts autocrine stimulation on murine t-cell leukaemia growth. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222760/ https://www.ncbi.nlm.nih.gov/pubmed/9083328 |
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