High levels of the extracellular matrix proteoglycan decorin are associated with inhibition of testicular function
Summary Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor (GF) signalling, thereby blocking downstream actions of GFs. In the present study the expression and regulation of DCN using both hum...
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Published in: | International journal of andrology Vol. 35; no. 4; pp. 550 - 561 |
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Blackwell Publishing Ltd
01-08-2012
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Abstract | Summary
Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor (GF) signalling, thereby blocking downstream actions of GFs. In the present study the expression and regulation of DCN using both human testes and two experimental animal models, namely the rhesus monkey and mouse, were examined. DCN protein was present in peritubular and interstitial areas of adult human and monkey testes, while it was almost undetectable in adult wild type mice. Interestingly, the levels and sites of testicular DCN expression in the monkeys were inversely correlated with testicular maturation markers. A strong DCN expression associated with the abundant connective tissue of the interstitial areas in the postnatal through pre‐pubertal phases was observed. In adult and old monkeys the DCN pattern was similar to the one in normal human testes, presenting strong expression at the peritubular region. In the testes of both infertile men and in a mouse model of inflammation associated infertility (aromatase‐overexpressing transgenic mice), the fibrotic changes and increased numbers of tumour necrosis factor (TNF)‐α‐producing immune cells were shown to be associated with increased production of DCN. Furthermore, studies with human testicular peritubular cells isolated from fibrotic testis indicated that TNF‐α significantly increased DCN production. The data, thus, show that an increased DCN level is associated with impaired testicular function, supporting our hypothesis that DCN interferes with paracrine signalling of the testis in health and disease. |
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AbstractList | Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor (GF) signaling, thereby blocking downstream actions of GFs. In the present study the expression and regulation of DCN using both human testes and two experimental animal models, namely the rhesus monkey and mouse, were examined. DCN protein was present in peritubular and interstitial areas of adult human and monkey testes, while it was almost undetectable in adult wild-type mice. Interestingly, the levels and sites of testicular DCN expression in the monkeys were inversely correlated with testicular maturation markers. A strong DCN expression associated with the abundant connective tissue of the interstitial areas in the postnatal through prepubertal phases was observed. In adult and old monkeys the DCN pattern was similar to the one in normal human testes, presenting strong expression at the peritubular region. In the testes of both infertile men and in a mouse model of inflammation associated infertility (aromatase-overexpressing transgenic mice), the fibrotic changes and increased numbers of Tumor necrosis factor (TNF)-α-producing immune cells were shown to be associated with increased production of DCN. Furthermore, studies with human testicular peritubular cells isolated from fibrotic testis indicated that TNF-α significantly increased DCN production. The data, thus, show that an increased DCN level is associated with impaired testicular function, supporting our hypothesis that DCN interferes with paracrine signaling of the testis in health and disease. Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor (GF) signalling, thereby blocking downstream actions of GFs. In the present study the expression and regulation of DCN using both human testes and two experimental animal models, namely the rhesus monkey and mouse, were examined. DCN protein was present in peritubular and interstitial areas of adult human and monkey testes, while it was almost undetectable in adult wild type mice. Interestingly, the levels and sites of testicular DCN expression in the monkeys were inversely correlated with testicular maturation markers. A strong DCN expression associated with the abundant connective tissue of the interstitial areas in the postnatal through pre‐pubertal phases was observed. In adult and old monkeys the DCN pattern was similar to the one in normal human testes, presenting strong expression at the peritubular region. In the testes of both infertile men and in a mouse model of inflammation associated infertility (aromatase‐overexpressing transgenic mice), the fibrotic changes and increased numbers of tumour necrosis factor (TNF)‐α‐producing immune cells were shown to be associated with increased production of DCN. Furthermore, studies with human testicular peritubular cells isolated from fibrotic testis indicated that TNF‐α significantly increased DCN production. The data, thus, show that an increased DCN level is associated with impaired testicular function, supporting our hypothesis that DCN interferes with paracrine signalling of the testis in health and disease. Summary Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor (GF) signalling, thereby blocking downstream actions of GFs. In the present study the expression and regulation of DCN using both human testes and two experimental animal models, namely the rhesus monkey and mouse, were examined. DCN protein was present in peritubular and interstitial areas of adult human and monkey testes, while it was almost undetectable in adult wild type mice. Interestingly, the levels and sites of testicular DCN expression in the monkeys were inversely correlated with testicular maturation markers. A strong DCN expression associated with the abundant connective tissue of the interstitial areas in the postnatal through pre‐pubertal phases was observed. In adult and old monkeys the DCN pattern was similar to the one in normal human testes, presenting strong expression at the peritubular region. In the testes of both infertile men and in a mouse model of inflammation associated infertility (aromatase‐overexpressing transgenic mice), the fibrotic changes and increased numbers of tumour necrosis factor (TNF)‐α‐producing immune cells were shown to be associated with increased production of DCN. Furthermore, studies with human testicular peritubular cells isolated from fibrotic testis indicated that TNF‐α significantly increased DCN production. The data, thus, show that an increased DCN level is associated with impaired testicular function, supporting our hypothesis that DCN interferes with paracrine signalling of the testis in health and disease. |
Author | Adam, M. Poutanen, M. Strauss, L. Ullrich Schwarzer, J. Garyfallou, V. T. Urbanski, H. F. Welsch, U. Köhn, F. M. Mayerhofer, A. |
AuthorAffiliation | 3 Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, 97239, USA 6 Department of Physiology and Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, 20520 Turku, Finland 1 Anatomy and Cell Biology, Ludwig-Maximilians-University Munich, D-80802 Munich, Germany 4 Andrologicum, D-80331 Munich, Germany 5 Praxis Urology-Andrology, D-85356 Freising, Germany 2 Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon 97006, USA |
AuthorAffiliation_xml | – name: 4 Andrologicum, D-80331 Munich, Germany – name: 2 Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon 97006, USA – name: 3 Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon, 97239, USA – name: 6 Department of Physiology and Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, 20520 Turku, Finland – name: 1 Anatomy and Cell Biology, Ludwig-Maximilians-University Munich, D-80802 Munich, Germany – name: 5 Praxis Urology-Andrology, D-85356 Freising, Germany |
Author_xml | – sequence: 1 givenname: M. surname: Adam fullname: Adam, M. organization: Anatomy and Cell Biology, Ludwig-Maximilians-University Munich, Munich, Germany – sequence: 2 givenname: H. F. surname: Urbanski fullname: Urbanski, H. F. organization: Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon, USA – sequence: 3 givenname: V. T. surname: Garyfallou fullname: Garyfallou, V. T. organization: Division of Neuroscience, Oregon National Primate Research Center, Beaverton, Oregon, USA – sequence: 4 givenname: U. surname: Welsch fullname: Welsch, U. organization: Anatomy and Cell Biology, Ludwig-Maximilians-University Munich, Munich, Germany – sequence: 5 givenname: F. M. surname: Köhn fullname: Köhn, F. M. organization: Andrologicum, Munich, Germany – sequence: 6 givenname: J. surname: Ullrich Schwarzer fullname: Ullrich Schwarzer, J. organization: Praxis Urology-Andrology, Freising, Germany – sequence: 7 givenname: L. surname: Strauss fullname: Strauss, L. organization: Department of Physiology and Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, Turku, Finland – sequence: 8 givenname: M. surname: Poutanen fullname: Poutanen, M. organization: Department of Physiology and Turku Center for Disease Modeling, Institute of Biomedicine, University of Turku, Turku, Finland – sequence: 9 givenname: A. surname: Mayerhofer fullname: Mayerhofer, A. organization: Anatomy and Cell Biology, Ludwig-Maximilians-University Munich, Munich, Germany |
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Keywords | Proteoglycan Animal model primates < animal models Rodentia mouse < animal models Inflammation testis Testicle infertility Male genital system Sterility Vertebrata Reproduction Mammalia Mouse Animal Fibrosis Development Extracellular matrix |
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Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth... Decorin (DCN), a component of the extracellular matrix of the peritubular wall and the interstitial areas of the human testis, can interact with growth factor... |
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SubjectTerms | Animals Biological and medical sciences Birth control Cells, Cultured Decorin - metabolism development Disease Models, Animal Extracellular Matrix Proteins - metabolism Fibrosis Fundamental and applied biological sciences. Psychology Gynecology. Andrology. Obstetrics Humans infertility Infertility, Male - pathology Inflammation Macaca mulatta Male Male genital diseases Mammalian male genital system Medical sciences Mice Mice, Transgenic mouse < animal models primates < animal models proteoglycan Signal Transduction Sterility. Assisted procreation testis Testis - cytology Testis - metabolism Testis - pathology Tumor Necrosis Factor-alpha - biosynthesis Vertebrates: reproduction |
Title | High levels of the extracellular matrix proteoglycan decorin are associated with inhibition of testicular function |
URI | https://api.istex.fr/ark:/67375/WNG-DN00TNVR-7/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1365-2605.2011.01225.x https://www.ncbi.nlm.nih.gov/pubmed/22413766 https://search.proquest.com/docview/1039202327 https://pubmed.ncbi.nlm.nih.gov/PMC3376671 |
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