Effect of epithelial debridement on human cornea proteoglycans

Detalhes bibliográficos
Autor(a) principal: Soriano, Eduardo Sone [UNIFESP]
Data de Publicação: 2001
Outros Autores: Campos, Mauro Silveira de Queiroz [UNIFESP], Aguiar, Jair Adriano Kopke [UNIFESP], Michelacci, Yara Maria [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/1128
http://dx.doi.org/10.1590/S0100-879X2001000300005
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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spelling Soriano, Eduardo Sone [UNIFESP]Campos, Mauro Silveira de Queiroz [UNIFESP]Aguiar, Jair Adriano Kopke [UNIFESP]Michelacci, Yara Maria [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2015-06-14T13:29:20Z2015-06-14T13:29:20Z2001-03-01Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001.0100-879Xhttp://repositorio.unifesp.br/handle/11600/1128http://dx.doi.org/10.1590/S0100-879X2001000300005S0100-879X2001000300005.pdfS0100-879X200100030000510.1590/S0100-879X2001000300005WOS:000167640800005Corneal 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 OftalmologiaSciELO325-331engAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Researchcorneal explantsde-epithelizationglycosaminoglycanproteoglycanEffect of epithelial debridement on human cornea proteoglycansinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS0100-879X2001000300005.pdfapplication/pdf216523${dspace.ui.url}/bitstream/11600/1128/1/S0100-879X2001000300005.pdf9134c61736adbf4d08d55be00853c1f4MD51open accessTEXTS0100-879X2001000300005.pdf.txtS0100-879X2001000300005.pdf.txtExtracted texttext/plain23551${dspace.ui.url}/bitstream/11600/1128/2/S0100-879X2001000300005.pdf.txt4a10a26b4fd323a1d02fbc43fe728415MD52open access11600/11282021-09-29 14:52:14.433open accessoai:repositorio.unifesp.br:11600/1128Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-09-29T17:52:14Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.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
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
title_full_unstemmed 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]
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.institution.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.eng.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.issued.fl_str_mv 2001-03-01
dc.date.accessioned.fl_str_mv 2015-06-14T13:29:20Z
dc.date.available.fl_str_mv 2015-06-14T13:29:20Z
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dc.identifier.citation.fl_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/1128
http://dx.doi.org/10.1590/S0100-879X2001000300005
dc.identifier.issn.none.fl_str_mv 0100-879X
dc.identifier.file.none.fl_str_mv S0100-879X2001000300005.pdf
dc.identifier.scielo.none.fl_str_mv S0100-879X2001000300005
dc.identifier.doi.none.fl_str_mv 10.1590/S0100-879X2001000300005
dc.identifier.wos.none.fl_str_mv WOS:000167640800005
identifier_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 34, n. 3, p. 325-331, 2001.
0100-879X
S0100-879X2001000300005.pdf
S0100-879X2001000300005
10.1590/S0100-879X2001000300005
WOS:000167640800005
url http://repositorio.unifesp.br/handle/11600/1128
http://dx.doi.org/10.1590/S0100-879X2001000300005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Brazilian Journal of Medical and Biological Research
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dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
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