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Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression

Tumor cells are surrounded by infiltrating inflammatory cells, such as lymphocytes, neutrophils, macrophages, and mast cells. A body of evidence indicates that mast cells are associated with various types of tumors. Although role of mast cells can be directly related to their granule content, their...

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Autores principales: de Souza, Devandir Antonio, Toso, Vanina Danuza, Campos, Maria Rita de Cássia, Lara, Vanessa Soares, Oliver, Constance, Jamur, Maria Célia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399855/
https://www.ncbi.nlm.nih.gov/pubmed/22815822
http://dx.doi.org/10.1371/journal.pone.0040790
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author de Souza, Devandir Antonio
Toso, Vanina Danuza
Campos, Maria Rita de Cássia
Lara, Vanessa Soares
Oliver, Constance
Jamur, Maria Célia
author_facet de Souza, Devandir Antonio
Toso, Vanina Danuza
Campos, Maria Rita de Cássia
Lara, Vanessa Soares
Oliver, Constance
Jamur, Maria Célia
author_sort de Souza, Devandir Antonio
collection PubMed
description Tumor cells are surrounded by infiltrating inflammatory cells, such as lymphocytes, neutrophils, macrophages, and mast cells. A body of evidence indicates that mast cells are associated with various types of tumors. Although role of mast cells can be directly related to their granule content, their function in angiogenesis and tumor progression remains obscure. This study aims to understand the role of mast cells in these processes. Tumors were chemically induced in BALB/c mice and tumor progression was divided into Phases I, II and III. Phase I tumors exhibited a large number of mast cells, which increased in phase II and remained unchanged in phase III. The expression of mouse mast cell protease (mMCP)-4, mMCP-5, mMCP-6, mMCP-7, and carboxypeptidase A were analyzed at the 3 stages. Our results show that with the exception of mMCP-4 expression of these mast cell chymase (mMCP-5), tryptases (mMCP-6 and 7), and carboxypeptidase A (mMC-CPA) increased during tumor progression. Chymase and tryptase activity increased at all stages of tumor progression whereas the number of mast cells remained constant from phase II to III. The number of new blood vessels increased significantly in phase I, while in phases II and III an enlargement of existing blood vessels occurred. In vitro, mMCP-6 and 7 are able to induce vessel formation. The present study suggests that mast cells are involved in induction of angiogenesis in the early stages of tumor development and in modulating blood vessel growth in the later stages of tumor progression.
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spelling pubmed-33998552012-07-19 Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression de Souza, Devandir Antonio Toso, Vanina Danuza Campos, Maria Rita de Cássia Lara, Vanessa Soares Oliver, Constance Jamur, Maria Célia PLoS One Research Article Tumor cells are surrounded by infiltrating inflammatory cells, such as lymphocytes, neutrophils, macrophages, and mast cells. A body of evidence indicates that mast cells are associated with various types of tumors. Although role of mast cells can be directly related to their granule content, their function in angiogenesis and tumor progression remains obscure. This study aims to understand the role of mast cells in these processes. Tumors were chemically induced in BALB/c mice and tumor progression was divided into Phases I, II and III. Phase I tumors exhibited a large number of mast cells, which increased in phase II and remained unchanged in phase III. The expression of mouse mast cell protease (mMCP)-4, mMCP-5, mMCP-6, mMCP-7, and carboxypeptidase A were analyzed at the 3 stages. Our results show that with the exception of mMCP-4 expression of these mast cell chymase (mMCP-5), tryptases (mMCP-6 and 7), and carboxypeptidase A (mMC-CPA) increased during tumor progression. Chymase and tryptase activity increased at all stages of tumor progression whereas the number of mast cells remained constant from phase II to III. The number of new blood vessels increased significantly in phase I, while in phases II and III an enlargement of existing blood vessels occurred. In vitro, mMCP-6 and 7 are able to induce vessel formation. The present study suggests that mast cells are involved in induction of angiogenesis in the early stages of tumor development and in modulating blood vessel growth in the later stages of tumor progression. Public Library of Science 2012-07-18 /pmc/articles/PMC3399855/ /pubmed/22815822 http://dx.doi.org/10.1371/journal.pone.0040790 Text en de Souza et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
de Souza, Devandir Antonio
Toso, Vanina Danuza
Campos, Maria Rita de Cássia
Lara, Vanessa Soares
Oliver, Constance
Jamur, Maria Célia
Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title_full Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title_fullStr Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title_full_unstemmed Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title_short Expression of Mast Cell Proteases Correlates with Mast Cell Maturation and Angiogenesis during Tumor Progression
title_sort expression of mast cell proteases correlates with mast cell maturation and angiogenesis during tumor progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399855/
https://www.ncbi.nlm.nih.gov/pubmed/22815822
http://dx.doi.org/10.1371/journal.pone.0040790
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