Effect of epithelial debridement on human cornea proteoglycans
Autor(a) principal: | |
---|---|
Data de Publicação: | 2001 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/0013000000b09 |
DOI: | 10.1590/S0100-879X2001000300005 |
Texto Completo: | http://dx.doi.org/10.1590/S0100-879X2001000300005 http://repositorio.unifesp.br/handle/11600/1128 |
Resumo: | Corneal transparency is attributed to the regular spacing and diameter of collagen fibrils, and proteoglycans may play a role in fibrillogenesis and matrix assembly. Corneal scar tissue is opaque and this opacity is explained by decreased ultrastructural order that may be related to proteoglycan composition. Thus, the objectives of the present study were to characterize the proteoglycans synthesized by human corneal explants and to investigate the effect of mechanical epithelial debridement. Human corneas unsuitable for transplants were immersed in F-12 culture medium and maintained under tissue culture conditions. The proteoglycans synthesized in 24 h were labeled metabolically by the addition of 35S-sulfate to the medium. These compounds were extracted by 4 M GuHCl and identified by a combination of agarose gel electrophoresis, enzymatic degradation with protease and mucopolysaccharidases, and immunoblotting. Decorin was identified as the main dermatan sulfate proteoglycan and keratan sulfate proteoglycans were also prominent components. When the glycosaminoglycan side chains were analyzed, only keratan sulfate and dermatan sulfate were detected (~50% each). Nevertheless, when these compounds were 35S-labeled metabolically, the label in dermatan sulfate was greater than in keratan sulfate, suggesting a lower synthesis rate for keratan sulfate. 35S-Heparan sulfate also appeared. The removal of the epithelial layer caused a decrease in heparan sulfate labeling and induced the synthesis of dermatan sulfate by the stroma. The increased deposit of dermatan sulfate proteoglycans in the stroma suggests a functional relationship between epithelium and stroma that could be related to the corneal opacity that may appear after epithelial cell debridement. |
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Effect of epithelial debridement on human cornea proteoglycanscorneal explantsde-epithelizationglycosaminoglycanproteoglycanCorneal transparency is attributed to the regular spacing and diameter of collagen fibrils, and proteoglycans may play a role in fibrillogenesis and matrix assembly. Corneal scar tissue is opaque and this opacity is explained by decreased ultrastructural order that may be related to proteoglycan composition. Thus, the objectives of the present study were to characterize the proteoglycans synthesized by human corneal explants and to investigate the effect of mechanical epithelial debridement. Human corneas unsuitable for transplants were immersed in F-12 culture medium and maintained under tissue culture conditions. The proteoglycans synthesized in 24 h were labeled metabolically by the addition of 35S-sulfate to the medium. These compounds were extracted by 4 M GuHCl and identified by a combination of agarose gel electrophoresis, enzymatic degradation with protease and mucopolysaccharidases, and immunoblotting. Decorin was identified as the main dermatan sulfate proteoglycan and keratan sulfate proteoglycans were also prominent components. When the glycosaminoglycan side chains were analyzed, only keratan sulfate and dermatan sulfate were detected (~50% each). Nevertheless, when these compounds were 35S-labeled metabolically, the label in dermatan sulfate was greater than in keratan sulfate, suggesting a lower synthesis rate for keratan sulfate. 35S-Heparan sulfate also appeared. The removal of the epithelial layer caused a decrease in heparan sulfate labeling and induced the synthesis of dermatan sulfate by the stroma. The increased deposit of dermatan sulfate proteoglycans in the stroma suggests a functional relationship between epithelium and stroma that could be related to the corneal opacity that may appear after epithelial cell debridement.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de BioquímicaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de OftalmologiaUNIFESP, EPM, Depto. de BioquímicaUNIFESP, EPM, Depto. de OftalmologiaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Soriano, Eduardo Sone [UNIFESP]Campos, Mauro Silveira de Queiroz [UNIFESP]Aguiar, Jair Adriano Kopke [UNIFESP]Michelacci, Yara Maria [UNIFESP]2015-06-14T13:29:20Z2015-06-14T13:29:20Z2001-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion325-331application/pdfhttp://dx.doi.org/10.1590/S0100-879X2001000300005Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001.10.1590/S0100-879X2001000300005S0100-879X2001000300005.pdf0100-879XS0100-879X2001000300005http://repositorio.unifesp.br/handle/11600/1128WOS:000167640800005ark:/48912/0013000000b09engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T16:51:24Zoai:repositorio.unifesp.br/:11600/1128Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T19:48:17.617970Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Effect of epithelial debridement on human cornea proteoglycans |
title |
Effect of epithelial debridement on human cornea proteoglycans |
spellingShingle |
Effect of epithelial debridement on human cornea proteoglycans Effect of epithelial debridement on human cornea proteoglycans Soriano, Eduardo Sone [UNIFESP] corneal explants de-epithelization glycosaminoglycan proteoglycan Soriano, Eduardo Sone [UNIFESP] corneal explants de-epithelization glycosaminoglycan proteoglycan |
title_short |
Effect of epithelial debridement on human cornea proteoglycans |
title_full |
Effect of epithelial debridement on human cornea proteoglycans |
title_fullStr |
Effect of epithelial debridement on human cornea proteoglycans Effect of epithelial debridement on human cornea proteoglycans |
title_full_unstemmed |
Effect of epithelial debridement on human cornea proteoglycans Effect of epithelial debridement on human cornea proteoglycans |
title_sort |
Effect of epithelial debridement on human cornea proteoglycans |
author |
Soriano, Eduardo Sone [UNIFESP] |
author_facet |
Soriano, Eduardo Sone [UNIFESP] Soriano, Eduardo Sone [UNIFESP] Campos, Mauro Silveira de Queiroz [UNIFESP] Aguiar, Jair Adriano Kopke [UNIFESP] Michelacci, Yara Maria [UNIFESP] Campos, Mauro Silveira de Queiroz [UNIFESP] Aguiar, Jair Adriano Kopke [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
author_role |
author |
author2 |
Campos, Mauro Silveira de Queiroz [UNIFESP] Aguiar, Jair Adriano Kopke [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Soriano, Eduardo Sone [UNIFESP] Campos, Mauro Silveira de Queiroz [UNIFESP] Aguiar, Jair Adriano Kopke [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
dc.subject.por.fl_str_mv |
corneal explants de-epithelization glycosaminoglycan proteoglycan |
topic |
corneal explants de-epithelization glycosaminoglycan proteoglycan |
description |
Corneal transparency is attributed to the regular spacing and diameter of collagen fibrils, and proteoglycans may play a role in fibrillogenesis and matrix assembly. Corneal scar tissue is opaque and this opacity is explained by decreased ultrastructural order that may be related to proteoglycan composition. Thus, the objectives of the present study were to characterize the proteoglycans synthesized by human corneal explants and to investigate the effect of mechanical epithelial debridement. Human corneas unsuitable for transplants were immersed in F-12 culture medium and maintained under tissue culture conditions. The proteoglycans synthesized in 24 h were labeled metabolically by the addition of 35S-sulfate to the medium. These compounds were extracted by 4 M GuHCl and identified by a combination of agarose gel electrophoresis, enzymatic degradation with protease and mucopolysaccharidases, and immunoblotting. Decorin was identified as the main dermatan sulfate proteoglycan and keratan sulfate proteoglycans were also prominent components. When the glycosaminoglycan side chains were analyzed, only keratan sulfate and dermatan sulfate were detected (~50% each). Nevertheless, when these compounds were 35S-labeled metabolically, the label in dermatan sulfate was greater than in keratan sulfate, suggesting a lower synthesis rate for keratan sulfate. 35S-Heparan sulfate also appeared. The removal of the epithelial layer caused a decrease in heparan sulfate labeling and induced the synthesis of dermatan sulfate by the stroma. The increased deposit of dermatan sulfate proteoglycans in the stroma suggests a functional relationship between epithelium and stroma that could be related to the corneal opacity that may appear after epithelial cell debridement. |
publishDate |
2001 |
dc.date.none.fl_str_mv |
2001-03-01 2015-06-14T13:29:20Z 2015-06-14T13:29:20Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0100-879X2001000300005 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001. 10.1590/S0100-879X2001000300005 S0100-879X2001000300005.pdf 0100-879X S0100-879X2001000300005 http://repositorio.unifesp.br/handle/11600/1128 WOS:000167640800005 |
dc.identifier.dark.fl_str_mv |
ark:/48912/0013000000b09 |
url |
http://dx.doi.org/10.1590/S0100-879X2001000300005 http://repositorio.unifesp.br/handle/11600/1128 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001. 10.1590/S0100-879X2001000300005 S0100-879X2001000300005.pdf 0100-879X S0100-879X2001000300005 WOS:000167640800005 ark:/48912/0013000000b09 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
325-331 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1822219252809072641 |
dc.identifier.doi.none.fl_str_mv |
10.1590/S0100-879X2001000300005 |