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Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle
BACKGROUND: One of the unique characteristics of the female genital tract is the extensive tissue remodeling observed throughout the menstrual cycle. Multiple components of the extracellular matrix take part in this tissue rebuilding; however, the individual components involved have not been identif...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489778/ https://www.ncbi.nlm.nih.gov/pubmed/22897899 http://dx.doi.org/10.1186/1477-7827-10-56 |
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author | Diaz, Patricia S Solar, Paula A Juica, Natalia E Orihuela, Pedro A Cardenas, Hugo Christodoulides, Myron Vargas, Renato Velasquez, Luis A |
author_facet | Diaz, Patricia S Solar, Paula A Juica, Natalia E Orihuela, Pedro A Cardenas, Hugo Christodoulides, Myron Vargas, Renato Velasquez, Luis A |
author_sort | Diaz, Patricia S |
collection | PubMed |
description | BACKGROUND: One of the unique characteristics of the female genital tract is the extensive tissue remodeling observed throughout the menstrual cycle. Multiple components of the extracellular matrix take part in this tissue rebuilding; however, the individual components involved have not been identified. METHODS: In the present study, the expression of extracellular matrix proteins and selected matrix metalloproteinase (MMP) activities in Fallopian tubes (FT) throughout the menstrual cycle were examined by PCR array, immunocytochemistry, zymography and bioinformatics. RESULTS: Of the eighty-four genes analyzed, eighty-three were expressed in the FT during at least one stage of the menstrual cycle. We observed a significant increase (>/=2-fold) in ADAMTS1, ADAMTS13, COL7A1, MMP3, MMP9, PECAM1, and THBS3 in the periovulatory phase compared to the follicular phase. Meanwhile, we observed a significant decrease (>/= 2-fold) in COL7A1, ICAM1, ITGA8, MMP16, MMP9, CLEC3B, SELE and TIMP2 in the lutheal phase compared to the periovulatory phase. Immunocytochemistry showed that MMP-3 and MMP-9 were localized in the endosalpinx during all phases of the menstrual cycle. Gelatin zymograms detected non-cycle-dependent protease activity. CONCLUSIONS: Several extracellular matrix components were regulated throughout the menstrual cycle in a cyclic pattern, suggesting a possible steroid regulation and a role in tissue remodeling and FT functions. |
format | Online Article Text |
id | pubmed-3489778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34897782012-11-06 Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle Diaz, Patricia S Solar, Paula A Juica, Natalia E Orihuela, Pedro A Cardenas, Hugo Christodoulides, Myron Vargas, Renato Velasquez, Luis A Reprod Biol Endocrinol Research BACKGROUND: One of the unique characteristics of the female genital tract is the extensive tissue remodeling observed throughout the menstrual cycle. Multiple components of the extracellular matrix take part in this tissue rebuilding; however, the individual components involved have not been identified. METHODS: In the present study, the expression of extracellular matrix proteins and selected matrix metalloproteinase (MMP) activities in Fallopian tubes (FT) throughout the menstrual cycle were examined by PCR array, immunocytochemistry, zymography and bioinformatics. RESULTS: Of the eighty-four genes analyzed, eighty-three were expressed in the FT during at least one stage of the menstrual cycle. We observed a significant increase (>/=2-fold) in ADAMTS1, ADAMTS13, COL7A1, MMP3, MMP9, PECAM1, and THBS3 in the periovulatory phase compared to the follicular phase. Meanwhile, we observed a significant decrease (>/= 2-fold) in COL7A1, ICAM1, ITGA8, MMP16, MMP9, CLEC3B, SELE and TIMP2 in the lutheal phase compared to the periovulatory phase. Immunocytochemistry showed that MMP-3 and MMP-9 were localized in the endosalpinx during all phases of the menstrual cycle. Gelatin zymograms detected non-cycle-dependent protease activity. CONCLUSIONS: Several extracellular matrix components were regulated throughout the menstrual cycle in a cyclic pattern, suggesting a possible steroid regulation and a role in tissue remodeling and FT functions. BioMed Central 2012-08-16 /pmc/articles/PMC3489778/ /pubmed/22897899 http://dx.doi.org/10.1186/1477-7827-10-56 Text en Copyright ©2012 Diaz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Diaz, Patricia S Solar, Paula A Juica, Natalia E Orihuela, Pedro A Cardenas, Hugo Christodoulides, Myron Vargas, Renato Velasquez, Luis A Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title | Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title_full | Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title_fullStr | Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title_full_unstemmed | Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title_short | Differential expression of extracellular matrix components in the Fallopian tubes throughout the menstrual cycle |
title_sort | differential expression of extracellular matrix components in the fallopian tubes throughout the menstrual cycle |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489778/ https://www.ncbi.nlm.nih.gov/pubmed/22897899 http://dx.doi.org/10.1186/1477-7827-10-56 |
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