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Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice

BACKGROUND: Implantation of the embryo and successful pregnancy are dependent on the differentiation of endometrial stromal cells into decidual cells. Female interleukin-11 receptor α (IL-11Rα) deficient mice are infertile due to disrupted decidualization, suggesting a critical role for IL-11 and it...

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Autores principales: White, Christine A, Robb, Lorraine, Salamonsen, Lois A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC535545/
https://www.ncbi.nlm.nih.gov/pubmed/15537430
http://dx.doi.org/10.1186/1477-7827-2-76
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author White, Christine A
Robb, Lorraine
Salamonsen, Lois A
author_facet White, Christine A
Robb, Lorraine
Salamonsen, Lois A
author_sort White, Christine A
collection PubMed
description BACKGROUND: Implantation of the embryo and successful pregnancy are dependent on the differentiation of endometrial stromal cells into decidual cells. Female interleukin-11 receptor α (IL-11Rα) deficient mice are infertile due to disrupted decidualization, suggesting a critical role for IL-11 and its target genes in implantation. The molecular targets of IL-11 in the uterus are unknown, but it is likely that IL-11 signaling modifies the expression of other genes important in decidualization. This study aimed to identify genes regulated by IL-11 during decidualization in mouse uterus, and to examine their expression and localization as an indication of functional significance during early pregnancy. METHODS: Decidualization was artificially induced in pseudopregnant wild type (IL11Ra(+/+)) and IL-11Rα deficient (IL11Ra(-/-)) littermates by oil injection into the uterine lumen, and gene expression analyzed by NIA 15K cDNA microarray analysis at subsequent time points. Quantitative real-time RT-PCR was used as an alternative mRNA quantitation method and the expression and cellular localization of the protein products was examined by immunohistochemistry. RESULTS: Among 15,247 DNA probes, 13 showed increased and 4 decreased expression in IL11Ra(-/-) uterus at 48 h of decidualization. These included 4 genes encoding extracellular matrix proteins; collagen III α1, secreted acidic cysteine-rich glycoprotein (SPARC), biglycan and nidogen-1 (entactin). Immunohistochemistry confirmed increased collagen III and biglycan protein expression in IL11Ra(-/-) uterus at this time. In both IL11Ra(-/-) and wild type uterus, collagen III and biglycan were primarily localized to the outer connective tissue and smooth muscle cells of the myometrium, with diffuse staining in the cytoplasm of decidualized stromal cells. CONCLUSION: These data suggest that IL-11 regulates changes in the uterine extracellular matrix that are necessary for decidualization.
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spelling pubmed-5355452004-12-12 Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice White, Christine A Robb, Lorraine Salamonsen, Lois A Reprod Biol Endocrinol Research BACKGROUND: Implantation of the embryo and successful pregnancy are dependent on the differentiation of endometrial stromal cells into decidual cells. Female interleukin-11 receptor α (IL-11Rα) deficient mice are infertile due to disrupted decidualization, suggesting a critical role for IL-11 and its target genes in implantation. The molecular targets of IL-11 in the uterus are unknown, but it is likely that IL-11 signaling modifies the expression of other genes important in decidualization. This study aimed to identify genes regulated by IL-11 during decidualization in mouse uterus, and to examine their expression and localization as an indication of functional significance during early pregnancy. METHODS: Decidualization was artificially induced in pseudopregnant wild type (IL11Ra(+/+)) and IL-11Rα deficient (IL11Ra(-/-)) littermates by oil injection into the uterine lumen, and gene expression analyzed by NIA 15K cDNA microarray analysis at subsequent time points. Quantitative real-time RT-PCR was used as an alternative mRNA quantitation method and the expression and cellular localization of the protein products was examined by immunohistochemistry. RESULTS: Among 15,247 DNA probes, 13 showed increased and 4 decreased expression in IL11Ra(-/-) uterus at 48 h of decidualization. These included 4 genes encoding extracellular matrix proteins; collagen III α1, secreted acidic cysteine-rich glycoprotein (SPARC), biglycan and nidogen-1 (entactin). Immunohistochemistry confirmed increased collagen III and biglycan protein expression in IL11Ra(-/-) uterus at this time. In both IL11Ra(-/-) and wild type uterus, collagen III and biglycan were primarily localized to the outer connective tissue and smooth muscle cells of the myometrium, with diffuse staining in the cytoplasm of decidualized stromal cells. CONCLUSION: These data suggest that IL-11 regulates changes in the uterine extracellular matrix that are necessary for decidualization. BioMed Central 2004-11-10 /pmc/articles/PMC535545/ /pubmed/15537430 http://dx.doi.org/10.1186/1477-7827-2-76 Text en Copyright © 2004 White 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
White, Christine A
Robb, Lorraine
Salamonsen, Lois A
Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title_full Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title_fullStr Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title_full_unstemmed Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title_short Uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
title_sort uterine extracellular matrix components are altered during defective decidualization in interleukin-11 receptor α deficient mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC535545/
https://www.ncbi.nlm.nih.gov/pubmed/15537430
http://dx.doi.org/10.1186/1477-7827-2-76
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