High glucose induces caspase-independent cell death in retinal neural cells
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/5333 https://doi.org/10.1016/j.nbd.2006.10.023 |
Resumo: | Diabetic retinopathy is a leading cause of blindness among adults in the western countries. It has been reported that neurodegeneration may occur in diabetic retinas, but the mechanisms underlying retinal cell death are poorly understood. We found that high glucose increased the number of cells with condensed nuclei and the number of TUNEL-positive cells, and caused an increase in the translocation of phosphatidylserine to the outer leaflet of the plasma membrane, indicating that high glucose induces apoptosis in cultured retinal neural cells. The activity of caspases did not increase in high glucose-treated cells, but apoptosis-inducing factor (AIF) levels decreased in the mitochondria and increased in the nucleus, indicating a translocation to the nucleus where it may cause DNA fragmentation. These results demonstrate that elevated glucose induces apoptosis in cultured retinal neural cells. The increase in apoptosis is not dependent on caspase activation, but is mediated through AIF release from the mitochondria. |
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High glucose induces caspase-independent cell death in retinal neural cellsApoptosisMitochondriaRetinopathyApoptosis-inducing factor (AIF)DiabetesDiabetic retinopathy is a leading cause of blindness among adults in the western countries. It has been reported that neurodegeneration may occur in diabetic retinas, but the mechanisms underlying retinal cell death are poorly understood. We found that high glucose increased the number of cells with condensed nuclei and the number of TUNEL-positive cells, and caused an increase in the translocation of phosphatidylserine to the outer leaflet of the plasma membrane, indicating that high glucose induces apoptosis in cultured retinal neural cells. The activity of caspases did not increase in high glucose-treated cells, but apoptosis-inducing factor (AIF) levels decreased in the mitochondria and increased in the nucleus, indicating a translocation to the nucleus where it may cause DNA fragmentation. These results demonstrate that elevated glucose induces apoptosis in cultured retinal neural cells. The increase in apoptosis is not dependent on caspase activation, but is mediated through AIF release from the mitochondria.http://www.sciencedirect.com/science/article/B6WNK-4MKCGWG-1/1/0b1383d4de478900bac3fea0f32aa8022007info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5333http://hdl.handle.net/10316/5333https://doi.org/10.1016/j.nbd.2006.10.023engNeurobiology of Disease. 25:3 (2007) 464-472Santiago, A. R.Cristóvão, A. J.Santos, P. F.Carvalho, C. M.Ambrósio, A. F.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-07-21T09:59:13Zoai:estudogeral.uc.pt:10316/5333Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:38.198543Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
High glucose induces caspase-independent cell death in retinal neural cells |
title |
High glucose induces caspase-independent cell death in retinal neural cells |
spellingShingle |
High glucose induces caspase-independent cell death in retinal neural cells Santiago, A. R. Apoptosis Mitochondria Retinopathy Apoptosis-inducing factor (AIF) Diabetes |
title_short |
High glucose induces caspase-independent cell death in retinal neural cells |
title_full |
High glucose induces caspase-independent cell death in retinal neural cells |
title_fullStr |
High glucose induces caspase-independent cell death in retinal neural cells |
title_full_unstemmed |
High glucose induces caspase-independent cell death in retinal neural cells |
title_sort |
High glucose induces caspase-independent cell death in retinal neural cells |
author |
Santiago, A. R. |
author_facet |
Santiago, A. R. Cristóvão, A. J. Santos, P. F. Carvalho, C. M. Ambrósio, A. F. |
author_role |
author |
author2 |
Cristóvão, A. J. Santos, P. F. Carvalho, C. M. Ambrósio, A. F. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santiago, A. R. Cristóvão, A. J. Santos, P. F. Carvalho, C. M. Ambrósio, A. F. |
dc.subject.por.fl_str_mv |
Apoptosis Mitochondria Retinopathy Apoptosis-inducing factor (AIF) Diabetes |
topic |
Apoptosis Mitochondria Retinopathy Apoptosis-inducing factor (AIF) Diabetes |
description |
Diabetic retinopathy is a leading cause of blindness among adults in the western countries. It has been reported that neurodegeneration may occur in diabetic retinas, but the mechanisms underlying retinal cell death are poorly understood. We found that high glucose increased the number of cells with condensed nuclei and the number of TUNEL-positive cells, and caused an increase in the translocation of phosphatidylserine to the outer leaflet of the plasma membrane, indicating that high glucose induces apoptosis in cultured retinal neural cells. The activity of caspases did not increase in high glucose-treated cells, but apoptosis-inducing factor (AIF) levels decreased in the mitochondria and increased in the nucleus, indicating a translocation to the nucleus where it may cause DNA fragmentation. These results demonstrate that elevated glucose induces apoptosis in cultured retinal neural cells. The increase in apoptosis is not dependent on caspase activation, but is mediated through AIF release from the mitochondria. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007 |
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://hdl.handle.net/10316/5333 http://hdl.handle.net/10316/5333 https://doi.org/10.1016/j.nbd.2006.10.023 |
url |
http://hdl.handle.net/10316/5333 https://doi.org/10.1016/j.nbd.2006.10.023 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Neurobiology of Disease. 25:3 (2007) 464-472 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
aplication/PDF |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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