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Distribution of extracellular matrix molecules in human uterine tubes during the menstrual cycle: a histological and immunohistochemical analysis
Indexado
WoS WOS:000434275300007
Scopus SCOPUS_ID:85045856856
DOI 10.1111/JOA.12814
Año 2018
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



The uterine tube (UT) is an important and complex organ of the women's reproductive system. In general, the anatomy and basic histology of this organ are well-known. However, the composition and function of the extracellular matrix (ECM) of the UT is still poorly understood. The ECM is a complex supramolecular material produced by cells which is commonly restricted to the basement membrane and interstitial spaces. ECM molecules play not only a structural role, they are also important for cell growth, survival and differentiation in all tissues. In this context, the aim of this study was to evaluate the deposition and distribution of type I and III collagens and proteoglycans (decorin, biglycan, fibromodulin and versican) in human UT during the follicular and luteal phases by using histochemical and immunohistochemical techniques. Our results showed a broad synthesis of collagens (I and III) in the stroma of the UT. The analysis by regions showed, in the mucosa, a specific distribution of versican and fibromodulin in the epithelial surface, whereas decorin and fibromodulin were observed in the lamina propria. Versican and decorin were found in the stroma of the muscular layer, whereas all studied proteoglycans were identified in the serosa. Curiously, biglycan was restricted to the wall of the blood vessels of the serosa and muscular layers. Furthermore, there was an immunoreaction for collagens, decorin, versican and fibromodulin in the UT peripheral nerves. The differential distribution of these ECM molecules in the different layers of the UT could be related to specific structural and/or biomechanical functions needed for the oviductal transport, successful fertilization and early embryogenesis. However, further molecular studies under physiological and pathological conditions are still needed to elucidate the specific role of each molecule in the human UT.

Revista



Revista ISSN
Journal Of Anatomy 0021-8782

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Disciplinas de Investigación



WOS
Anatomy & Morphology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Godoy-Guzman, Carlos Hombre UNIV GRANADA - España
Universidad de Santiago de Chile - Chile
Universidad de Granada, Facultad de Medicina - España
Universidad de Granada - España
2 NUNEZ-LAGOS, CLAUDIO FERNANDO Hombre Hospital San José - Chile
3 ORIHUELA-DIAZ, PEDRO ALEJANDRO Hombre Universidad de Santiago de Chile - Chile
Centro para el Desarrollo de la Nanociencia y la Nanotecnologia - Chile
4 CAMPOS-GONZALEZ, AMERICA Hombre UNIV GRANADA - España
Inst Invest Biosanitaria Ibs GRANADA - España
Universidad de Granada, Facultad de Medicina - España
Instituto de Investigación Biosanitaria ibs.GRANADA - España
5 CARRIEL-ARAYA, VICTOR SEBASTIAN Hombre UNIV GRANADA - España
Inst Invest Biosanitaria Ibs GRANADA - España
Universidad de Granada, Facultad de Medicina - España
Instituto de Investigación Biosanitaria ibs.GRANADA - España

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Financiamiento



Fuente
DICYT
National Institutes of Health
Universidad de Santiago de Chile
National Institute of Dental and Craniofacial Research
Departamento de Investigaciones Científicas y Tecnológicas, Universidad de Santiago de Chile
Tissue Engineering Group from the Department of Histology, University of Granada, Spain
Vicerrectoria de Investigacion, Desarrollo e Innovacion of Universidad de Santiago de Chile (USACH)
Servicio Murciano de Salud
Department of Histology, University of Granada

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Agradecimientos



Agradecimiento
This study was supported by the Tissue Engineering Group (CTS-115) from the Department of Histology, University of Granada, Spain, and by the research Grant from DICYT no. 021501GG, Vicerrectoria de Investigacion, Desarrollo e Innovacion of Universidad de Santiago de Chile (USACH) Proyecto Basal FB0807. The authors thank Dr Larry Fisher from the National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD, USA, for providing the rabbit anti-fibromodulin polyclonal (LF-150) antibody for this study. The authors are grateful to Dr. Ariane Ruyffelaert for her assistance with the English text. This work forms part of doctoral thesis of Carlos Godoy-Guzman.
This study was supported by the Tissue Engineering Group (CTS-115) from the Department of Histology, University of Granada, Spain, and by the research Grant from DICYT no. 021501GG, Vicerrector?a de Investigaci?n, Desarrollo e Innovaci?n of Universidad de Santiago de Chile (USACH) Proyecto Basal FB0807. The authors thank Dr Larry Fisher from the National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD, USA, for providing the rabbit anti-fibromodulin polyclonal (LF-150) antibody for this study. The authors are grateful to Dr. Ariane Ruyffelaert for her assistance with the English text. This work forms part of doctoral thesis of Carlos Godoy-Guzm?n.

Muestra la fuente de financiamiento declarada en la publicación.