Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis

Detalhes bibliográficos
Autor(a) principal: de Santi, Fabiane
Data de Publicação: 2020
Outros Autores: Lunardi, Isadora Dantas [UNESP], Beltrame, Flávia Luciana, Cerri, Paulo Sérgio [UNESP], Sasso-Cerri, Estela [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1530/REP-19-0462
http://hdl.handle.net/11449/200309
Resumo: In epididymis, cimetidine induces androgenic failure due to reduced sex hormone-binding globulin stromal levels and blockade of androgen receptor (AR) nuclear import. UCHL1, a hydrolase of ubiquitin-proteasome system (UPS), seems to play a role in autophagy and apoptotic pathway. However, the role of UPS and autophagy in epididymis has not been clarified. We evaluated UCHL1 and autophagy in epididymal cauda epithelium under androgenic deficiency induced by cimetidine, focusing on the interplay among these processes and apoptosis. The integrity of epididymal muscular layer was also evaluated. Male rats received cimetidine (CMTG) or saline (CG). Seminal vesicles were weighed, the expression of androgen-responsive genes Crisp1 and connexin 43 (Cx43) in cauda epididymis was evaluated, and cauda fragments were processed for light and transmission electron microscopy. The epithelium height and muscular thickness were measured. TUNEL, immunohistochemistry for caspase-3 and Cx43, and immunofluorescence for AR, Bcl-2, UCHL1, MAP LC3A, and p62/SQSTM1 (autophagic markers) were performed. Bcl-2, UCHL1, and Cx43 were detected by Western blot. In CMTG, the reduction in seminal vesicles weight accompanied by downregulation of Crisp1 and Cx43 confirmed epididymal androgenic failure. These results were associated with muscular atrophy, apoptosis and weak Cx43 and AR immunoexpression, supporting the androgenic dependence of muscular integrity. The high UCHL1 levels and reduction in Bcl-2 reinforce UCHL1 role in epithelial cells death. The intense immunoexpression of LC3A and p62/SQSTM1 indicates autophagic disturb, which in association with high UCHL1 levels, points to a role of UPS and autophagy in the regulation of epididymal epithelial cells viability under androgenic control.
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spelling Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymisIn epididymis, cimetidine induces androgenic failure due to reduced sex hormone-binding globulin stromal levels and blockade of androgen receptor (AR) nuclear import. UCHL1, a hydrolase of ubiquitin-proteasome system (UPS), seems to play a role in autophagy and apoptotic pathway. However, the role of UPS and autophagy in epididymis has not been clarified. We evaluated UCHL1 and autophagy in epididymal cauda epithelium under androgenic deficiency induced by cimetidine, focusing on the interplay among these processes and apoptosis. The integrity of epididymal muscular layer was also evaluated. Male rats received cimetidine (CMTG) or saline (CG). Seminal vesicles were weighed, the expression of androgen-responsive genes Crisp1 and connexin 43 (Cx43) in cauda epididymis was evaluated, and cauda fragments were processed for light and transmission electron microscopy. The epithelium height and muscular thickness were measured. TUNEL, immunohistochemistry for caspase-3 and Cx43, and immunofluorescence for AR, Bcl-2, UCHL1, MAP LC3A, and p62/SQSTM1 (autophagic markers) were performed. Bcl-2, UCHL1, and Cx43 were detected by Western blot. In CMTG, the reduction in seminal vesicles weight accompanied by downregulation of Crisp1 and Cx43 confirmed epididymal androgenic failure. These results were associated with muscular atrophy, apoptosis and weak Cx43 and AR immunoexpression, supporting the androgenic dependence of muscular integrity. The high UCHL1 levels and reduction in Bcl-2 reinforce UCHL1 role in epithelial cells death. The intense immunoexpression of LC3A and p62/SQSTM1 indicates autophagic disturb, which in association with high UCHL1 levels, points to a role of UPS and autophagy in the regulation of epididymal epithelial cells viability under androgenic control.Department of Morphology and Genetics Federal University of São Paulo (UNIFESP/EPM)Laboratory of Histology and Embryology Department of Morphology Genetics Orthodontics and Pediatric Dentistry Dental School - São Paulo State University (UNESP/FOAr)Laboratory of Histology and Embryology Department of Morphology Genetics Orthodontics and Pediatric Dentistry Dental School - São Paulo State University (UNESP/FOAr)Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)de Santi, FabianeLunardi, Isadora Dantas [UNESP]Beltrame, Flávia LucianaCerri, Paulo Sérgio [UNESP]Sasso-Cerri, Estela [UNESP]2020-12-12T02:03:16Z2020-12-12T02:03:16Z2020-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article693-705http://dx.doi.org/10.1530/REP-19-0462Reproduction (Cambridge, England), v. 159, n. 6, p. 693-705, 2020.1741-7899http://hdl.handle.net/11449/20030910.1530/REP-19-04622-s2.0-85083622700Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengReproduction (Cambridge, England)info:eu-repo/semantics/openAccess2021-10-23T10:18:07Zoai:repositorio.unesp.br:11449/200309Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:55:39.198308Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
title Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
spellingShingle Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
de Santi, Fabiane
title_short Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
title_full Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
title_fullStr Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
title_full_unstemmed Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
title_sort Muscular atrophy, impaired epithelial autophagy and UCHL1 increase in androgen-deficient cauda epididymis
author de Santi, Fabiane
author_facet de Santi, Fabiane
Lunardi, Isadora Dantas [UNESP]
Beltrame, Flávia Luciana
Cerri, Paulo Sérgio [UNESP]
Sasso-Cerri, Estela [UNESP]
author_role author
author2 Lunardi, Isadora Dantas [UNESP]
Beltrame, Flávia Luciana
Cerri, Paulo Sérgio [UNESP]
Sasso-Cerri, Estela [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv de Santi, Fabiane
Lunardi, Isadora Dantas [UNESP]
Beltrame, Flávia Luciana
Cerri, Paulo Sérgio [UNESP]
Sasso-Cerri, Estela [UNESP]
description In epididymis, cimetidine induces androgenic failure due to reduced sex hormone-binding globulin stromal levels and blockade of androgen receptor (AR) nuclear import. UCHL1, a hydrolase of ubiquitin-proteasome system (UPS), seems to play a role in autophagy and apoptotic pathway. However, the role of UPS and autophagy in epididymis has not been clarified. We evaluated UCHL1 and autophagy in epididymal cauda epithelium under androgenic deficiency induced by cimetidine, focusing on the interplay among these processes and apoptosis. The integrity of epididymal muscular layer was also evaluated. Male rats received cimetidine (CMTG) or saline (CG). Seminal vesicles were weighed, the expression of androgen-responsive genes Crisp1 and connexin 43 (Cx43) in cauda epididymis was evaluated, and cauda fragments were processed for light and transmission electron microscopy. The epithelium height and muscular thickness were measured. TUNEL, immunohistochemistry for caspase-3 and Cx43, and immunofluorescence for AR, Bcl-2, UCHL1, MAP LC3A, and p62/SQSTM1 (autophagic markers) were performed. Bcl-2, UCHL1, and Cx43 were detected by Western blot. In CMTG, the reduction in seminal vesicles weight accompanied by downregulation of Crisp1 and Cx43 confirmed epididymal androgenic failure. These results were associated with muscular atrophy, apoptosis and weak Cx43 and AR immunoexpression, supporting the androgenic dependence of muscular integrity. The high UCHL1 levels and reduction in Bcl-2 reinforce UCHL1 role in epithelial cells death. The intense immunoexpression of LC3A and p62/SQSTM1 indicates autophagic disturb, which in association with high UCHL1 levels, points to a role of UPS and autophagy in the regulation of epididymal epithelial cells viability under androgenic control.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T02:03:16Z
2020-12-12T02:03:16Z
2020-05-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1530/REP-19-0462
Reproduction (Cambridge, England), v. 159, n. 6, p. 693-705, 2020.
1741-7899
http://hdl.handle.net/11449/200309
10.1530/REP-19-0462
2-s2.0-85083622700
url http://dx.doi.org/10.1530/REP-19-0462
http://hdl.handle.net/11449/200309
identifier_str_mv Reproduction (Cambridge, England), v. 159, n. 6, p. 693-705, 2020.
1741-7899
10.1530/REP-19-0462
2-s2.0-85083622700
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Reproduction (Cambridge, England)
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 693-705
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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