Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid
- Autores
- Politi, Luis Enrique; Rotstein, Nora Patricia; Carri, Néstor Gabriel
- Año de publicación
- 2001
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Purpose. In a previous study, it was reported that docosahexaenoic acid (DHA) is essential to postpone apoptosis and to promote differentiation of rat retina photoreceptors in vitro. In the current study, the protective effects of GDNF on photoreceptor cells during development in vitro and its action when combined with DHA were investigated. Methods. Rat retina neuronal cultures were incubated in a chemically defined medium, either without photoreceptor survival factors or supplemented with GDNF, DHA, or GDNF plus DHA. Evolution of survival, apoptosis, opsin expression, mitochondrial functioning, and cell proliferation were investigated at different times of development in vitro. Results. Incubation with GDNF selectively increased the number of surviving photoreceptors, reduced their apoptosis, and augmented opsin expression. Proliferative cell nuclei antigen (PCNA) determination and addition of [3H]-thymidine or bromodeoxyuridine showed that GDNF promoted neuroblast proliferation during the first hours of development in vitro. The combined addition of GDNF and DHA enhanced opsin expression and photoreceptor survival in an additive manner. The advance of photoreceptor apoptosis in cultures without trophic factors correlated with an increased impairment in mitochondrial functionality. Addition of GDNF and DHA significantly diminished the loss of mitochondrial activity. Conclusions. These results show that GDNF stimulated the cell cycle progression, leading to neuroblast proliferation at early stages of development, and delayed the onset of apoptosis later on, improving differentiation and acting as a trophic factor for photoreceptors. The combination of GDNF with DHA had an additive effect both on photoreceptor survival and on opsin expression. Preservation of mitochondrial function may be involved in the antiapoptotic effect of both factors.
Instituto Multidisciplinario de Biología Celular - Materia
-
Ciencias Exactas
Ciencias Médicas
Photoreceptor survival
Apoptosis
Docosahexaenoic acid
Neuroblast - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/99746
Ver los metadatos del registro completo
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Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acidPoliti, Luis EnriqueRotstein, Nora PatriciaCarri, Néstor GabrielCiencias ExactasCiencias MédicasPhotoreceptor survivalApoptosisDocosahexaenoic acidNeuroblastPurpose. In a previous study, it was reported that docosahexaenoic acid (DHA) is essential to postpone apoptosis and to promote differentiation of rat retina photoreceptors in vitro. In the current study, the protective effects of GDNF on photoreceptor cells during development in vitro and its action when combined with DHA were investigated. Methods. Rat retina neuronal cultures were incubated in a chemically defined medium, either without photoreceptor survival factors or supplemented with GDNF, DHA, or GDNF plus DHA. Evolution of survival, apoptosis, opsin expression, mitochondrial functioning, and cell proliferation were investigated at different times of development in vitro. Results. Incubation with GDNF selectively increased the number of surviving photoreceptors, reduced their apoptosis, and augmented opsin expression. Proliferative cell nuclei antigen (PCNA) determination and addition of [<sup>3</sup>H]-thymidine or bromodeoxyuridine showed that GDNF promoted neuroblast proliferation during the first hours of development in vitro. The combined addition of GDNF and DHA enhanced opsin expression and photoreceptor survival in an additive manner. The advance of photoreceptor apoptosis in cultures without trophic factors correlated with an increased impairment in mitochondrial functionality. Addition of GDNF and DHA significantly diminished the loss of mitochondrial activity. Conclusions. These results show that GDNF stimulated the cell cycle progression, leading to neuroblast proliferation at early stages of development, and delayed the onset of apoptosis later on, improving differentiation and acting as a trophic factor for photoreceptors. The combination of GDNF with DHA had an additive effect both on photoreceptor survival and on opsin expression. Preservation of mitochondrial function may be involved in the antiapoptotic effect of both factors.Instituto Multidisciplinario de Biología Celular2001-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf3008-3015http://sedici.unlp.edu.ar/handle/10915/99746enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/53101info:eu-repo/semantics/altIdentifier/url/https://iovs.arvojournals.org/article.aspx?articleid=2123098info:eu-repo/semantics/altIdentifier/issn/0146-0404info:eu-repo/semantics/altIdentifier/hdl/11336/53101info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:52:22Zoai:sedici.unlp.edu.ar:10915/99746Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:52:22.29SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
title |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
spellingShingle |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid Politi, Luis Enrique Ciencias Exactas Ciencias Médicas Photoreceptor survival Apoptosis Docosahexaenoic acid Neuroblast |
title_short |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
title_full |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
title_fullStr |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
title_full_unstemmed |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
title_sort |
Effect of GDNF on neuroblast proliferation and photoreceptor survival: additive protection with docosahexaenoic acid |
dc.creator.none.fl_str_mv |
Politi, Luis Enrique Rotstein, Nora Patricia Carri, Néstor Gabriel |
author |
Politi, Luis Enrique |
author_facet |
Politi, Luis Enrique Rotstein, Nora Patricia Carri, Néstor Gabriel |
author_role |
author |
author2 |
Rotstein, Nora Patricia Carri, Néstor Gabriel |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Ciencias Médicas Photoreceptor survival Apoptosis Docosahexaenoic acid Neuroblast |
topic |
Ciencias Exactas Ciencias Médicas Photoreceptor survival Apoptosis Docosahexaenoic acid Neuroblast |
dc.description.none.fl_txt_mv |
Purpose. In a previous study, it was reported that docosahexaenoic acid (DHA) is essential to postpone apoptosis and to promote differentiation of rat retina photoreceptors in vitro. In the current study, the protective effects of GDNF on photoreceptor cells during development in vitro and its action when combined with DHA were investigated. Methods. Rat retina neuronal cultures were incubated in a chemically defined medium, either without photoreceptor survival factors or supplemented with GDNF, DHA, or GDNF plus DHA. Evolution of survival, apoptosis, opsin expression, mitochondrial functioning, and cell proliferation were investigated at different times of development in vitro. Results. Incubation with GDNF selectively increased the number of surviving photoreceptors, reduced their apoptosis, and augmented opsin expression. Proliferative cell nuclei antigen (PCNA) determination and addition of [<sup>3</sup>H]-thymidine or bromodeoxyuridine showed that GDNF promoted neuroblast proliferation during the first hours of development in vitro. The combined addition of GDNF and DHA enhanced opsin expression and photoreceptor survival in an additive manner. The advance of photoreceptor apoptosis in cultures without trophic factors correlated with an increased impairment in mitochondrial functionality. Addition of GDNF and DHA significantly diminished the loss of mitochondrial activity. Conclusions. These results show that GDNF stimulated the cell cycle progression, leading to neuroblast proliferation at early stages of development, and delayed the onset of apoptosis later on, improving differentiation and acting as a trophic factor for photoreceptors. The combination of GDNF with DHA had an additive effect both on photoreceptor survival and on opsin expression. Preservation of mitochondrial function may be involved in the antiapoptotic effect of both factors. Instituto Multidisciplinario de Biología Celular |
description |
Purpose. In a previous study, it was reported that docosahexaenoic acid (DHA) is essential to postpone apoptosis and to promote differentiation of rat retina photoreceptors in vitro. In the current study, the protective effects of GDNF on photoreceptor cells during development in vitro and its action when combined with DHA were investigated. Methods. Rat retina neuronal cultures were incubated in a chemically defined medium, either without photoreceptor survival factors or supplemented with GDNF, DHA, or GDNF plus DHA. Evolution of survival, apoptosis, opsin expression, mitochondrial functioning, and cell proliferation were investigated at different times of development in vitro. Results. Incubation with GDNF selectively increased the number of surviving photoreceptors, reduced their apoptosis, and augmented opsin expression. Proliferative cell nuclei antigen (PCNA) determination and addition of [<sup>3</sup>H]-thymidine or bromodeoxyuridine showed that GDNF promoted neuroblast proliferation during the first hours of development in vitro. The combined addition of GDNF and DHA enhanced opsin expression and photoreceptor survival in an additive manner. The advance of photoreceptor apoptosis in cultures without trophic factors correlated with an increased impairment in mitochondrial functionality. Addition of GDNF and DHA significantly diminished the loss of mitochondrial activity. Conclusions. These results show that GDNF stimulated the cell cycle progression, leading to neuroblast proliferation at early stages of development, and delayed the onset of apoptosis later on, improving differentiation and acting as a trophic factor for photoreceptors. The combination of GDNF with DHA had an additive effect both on photoreceptor survival and on opsin expression. Preservation of mitochondrial function may be involved in the antiapoptotic effect of both factors. |
publishDate |
2001 |
dc.date.none.fl_str_mv |
2001-11 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/99746 |
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http://sedici.unlp.edu.ar/handle/10915/99746 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
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openAccess |
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