Publication:
HSP47 expression in the hamster Sertoli cell: An immunohistochemical study

dc.contributor.authorSerrano-Sánchez, María Isabel
dc.contributor.authorFerrer, Concepción
dc.contributor.authorBeltrán Frutos, Ester
dc.contributor.authorMartínez Hernández, Jesús
dc.contributor.authorPastor García, Luis Miguel
dc.contributor.authorSeco Rovira, Vicente
dc.date.accessioned2024-10-01T11:22:04Z
dc.date.available2024-10-01T11:22:04Z
dc.date.issued2024
dc.description.abstractHSP47, a chaperone whose main function is the maturation of collagen molecules, is considered a marker of fibrotic diseases. Increased collagen synthesis in the testis has been associated with various pathologies leading to seminiferous tubule regression. Our aim was to study whether HSP47 is expressed in hamster Sertoli cells both in the adult and in two physiological situations of seminiferous tubule atrophy: irreversible testicular ageing and testicular regression due to short photoperiod (reversible). Eighteen animals were divided as follows: a group of 6 young animals aged 6 months, a group of 6 animals aged 24 months, which were exposed to a long photoperiod, and a final group of 6 young animals subjected to a short photoperiod. Testicular samples were fixed in methacarn and an immuno-histochemical technique was used to detect HSP47. A semiquantitative study of this protein expression was performed between tubular sections of aged animals with complete spermatogenesis and arrested spermatogenesis and tubular sections with arrest spermatogenesis of photoinhibited testes. Sertoli cells were positive for HSP47, the intensity being greater in tubular sections with arrested spermatogenesis in both aged and photoinhibited animals. Semiquantitative analysis corroborated this observation in the sense that the expression of this protein differed according to the functional state of the seminiferous tubules. Thus, the ratio of immunoreactivity was significantly higher in tubular sections with arrested spermatogenesis in aged animals compared with regressed animals, and in the latter compared with those whose tubular sections showed complete spermatogenesis. In conclusion, HSP47 expression in Sertoli cells was found for the first time in mammals. Moreover, increased expression seemed to be related to the degree of seminiferous atrophy epithelium and to the reversible or nonreversible physiological state of this epithelium.es
dc.formatapplication/pdfes
dc.format.extent8es
dc.identifier.citationHistology and Histopathology, Vol.39, nº10, (2024)
dc.identifier.doihttps://doi.org/10.14670/HH-18-734
dc.identifier.issn1699-5848
dc.identifier.issn0213-3911
dc.identifier.urihttp://hdl.handle.net/10201/144457
dc.languageenges
dc.publisherUniversidad de Murcia. Departamento de Biología Celular e Histologíaes
dc.relationSin financiación externa a la Universidades
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectSertoli celles
dc.subjectSyrian hamsteres
dc.subjectTesteses
dc.subjectHSP47es
dc.subjectAginges
dc.subjectPhotoperiodes
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncologíaes
dc.titleHSP47 expression in the hamster Sertoli cell: An immunohistochemical studyes
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
relation.isAuthorOfPublicationc3f97383-2754-4cb2-8046-a4f10bdce2e3
relation.isAuthorOfPublicatione442a579-c2af-4fdd-8e39-00e5581604cb
relation.isAuthorOfPublication920d1ad2-1252-4ca8-9187-f3a351c89ce2
relation.isAuthorOfPublication2d13647b-b273-48d7-840a-82a6350f3451
relation.isAuthorOfPublication.latestForDiscoveryc3f97383-2754-4cb2-8046-a4f10bdce2e3
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Seco-Rovira-39-1295-1302-2024.pdf
Size:
3.46 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
2.26 KB
Format:
Item-specific license agreed upon to submission
Description: