In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion
- Autores
- Bolognani, Federico; Albariño, César G.; Romanowski, Víctor; Carri, Néstor Gabriel; Goya, Rodolfo Gustavo
- Año de publicación
- 2001
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Objective: Herpes simplex virus type 1 (HSV-1)-derived vectors are known to be effective tools to deliver transgenes into normal and neoplastic anterior pituitary (AP) cells in vitro. Our objective was to assess the in vitro and in vivo effects of tsK/β-gal, a temperature-sensitive HSV-1-derived vector harbouring the E. coli β-galactosidase gene, on AP hormone secretion as well as on transgene expression in rat AP tumours (hyperplastic prolactinomas). Design: The impact of vector infection on prolactin (PRL) and GH release was determined in vitro in normal and hyperplastic (lactotrophic) dispersed AP cells exposed for 24 h to tsK/β-gal as well as in vivo in ectopic AP grafts. In some oestrogen-induced prolactinoma-carrying rats, vector suspension was stereotaxically injected into the glands to assess transgene expression in vivo. Methods: GH and PRL release was measured by specific RIAs. In vivo transgene expression was assessed by immunohistochemistry for β-galactosidase and enzymohistochemistry (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside). Ectopic pituitary grafts and stereotaxic surgery were performed following standard procedures. Results: At a multiplicity of infection of 0.5, the vector induced a 30 and 22% fall in PRL and GH release respectively in normal AP cells, whereas the corresponding hormone release inhibition for hyperplastic AP cells was 41 and 33% for PRL and GH respectively. In ectopic pituitary grafts, the effect of vector infection on hormone secretion was assessed by measuring serum PRL levels in the host rats every 5 days for 4 weeks post-grafting. In the pituitary-grafted rats that received the viral vector, serum PRL failed to increase to the levels achieved in control-grafted animals. Finally, pituitary tumours stereotaxically injected with tsK/β-gal showed widespread expression of the β-galactosidase transgene around the injection areas. Conclusions: The results reported here have implications for basic studies using gene transfer to pituitary gland as well as potential gene therapy approaches to pituitary diseases.
Instituto de Investigaciones Bioquímicas de La Plata
Instituto de Biotecnologia y Biologia Molecular
Instituto Multidisciplinario de Biología Celular - Materia
-
Ciencias Médicas
Ciencias Exactas
pituitary gland
hormone secretion - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
.jpg)
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/83484
Ver los metadatos del registro completo
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In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretionBolognani, FedericoAlbariño, César G.Romanowski, VíctorCarri, Néstor GabrielGoya, Rodolfo GustavoCiencias MédicasCiencias Exactaspituitary glandhormone secretionObjective: Herpes simplex virus type 1 (HSV-1)-derived vectors are known to be effective tools to deliver transgenes into normal and neoplastic anterior pituitary (AP) cells <i>in vitro</i>. Our objective was to assess the <i>in vitro</i> and <i>in vivo</i> effects of tsK/β-gal, a temperature-sensitive HSV-1-derived vector harbouring the <i>E. coli</i> β-galactosidase gene, on AP hormone secretion as well as on transgene expression in rat AP tumours (hyperplastic prolactinomas). Design: The impact of vector infection on prolactin (PRL) and GH release was determined <i>in vitro</i> in normal and hyperplastic (lactotrophic) dispersed AP cells exposed for 24 h to tsK/β-gal as well as <i>in vivo</i> in ectopic AP grafts. In some oestrogen-induced prolactinoma-carrying rats, vector suspension was stereotaxically injected into the glands to assess transgene expression <i>in vivo</i>. Methods: GH and PRL release was measured by specific RIAs. <i>In vivo</i> transgene expression was assessed by immunohistochemistry for β-galactosidase and enzymohistochemistry (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside). Ectopic pituitary grafts and stereotaxic surgery were performed following standard procedures. Results: At a multiplicity of infection of 0.5, the vector induced a 30 and 22% fall in PRL and GH release respectively in normal AP cells, whereas the corresponding hormone release inhibition for hyperplastic AP cells was 41 and 33% for PRL and GH respectively. In ectopic pituitary grafts, the effect of vector infection on hormone secretion was assessed by measuring serum PRL levels in the host rats every 5 days for 4 weeks post-grafting. In the pituitary-grafted rats that received the viral vector, serum PRL failed to increase to the levels achieved in control-grafted animals. Finally, pituitary tumours stereotaxically injected with tsK/β-gal showed widespread expression of the β-galactosidase transgene around the injection areas. Conclusions: The results reported here have implications for basic studies using gene transfer to pituitary gland as well as potential gene therapy approaches to pituitary diseases.Instituto de Investigaciones Bioquímicas de La PlataInstituto de Biotecnologia y Biologia MolecularInstituto Multidisciplinario de Biología Celular2001info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf497-503http://sedici.unlp.edu.ar/handle/10915/83484enginfo:eu-repo/semantics/altIdentifier/issn/0804-4643info:eu-repo/semantics/altIdentifier/doi/10.1530/eje.0.1450497info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:07:47Zoai:sedici.unlp.edu.ar:10915/83484Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:07:47.213SEDICI (UNLP) - Universidad Nacional de La Platafalse |
| dc.title.none.fl_str_mv |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| title |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| spellingShingle |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion Bolognani, Federico Ciencias Médicas Ciencias Exactas pituitary gland hormone secretion |
| title_short |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| title_full |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| title_fullStr |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| title_full_unstemmed |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| title_sort |
In vitro and in vivo herpetic vector-mediated gene transfer in the pituitary gland: Impact on hormone secretion |
| dc.creator.none.fl_str_mv |
Bolognani, Federico Albariño, César G. Romanowski, Víctor Carri, Néstor Gabriel Goya, Rodolfo Gustavo |
| author |
Bolognani, Federico |
| author_facet |
Bolognani, Federico Albariño, César G. Romanowski, Víctor Carri, Néstor Gabriel Goya, Rodolfo Gustavo |
| author_role |
author |
| author2 |
Albariño, César G. Romanowski, Víctor Carri, Néstor Gabriel Goya, Rodolfo Gustavo |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Ciencias Médicas Ciencias Exactas pituitary gland hormone secretion |
| topic |
Ciencias Médicas Ciencias Exactas pituitary gland hormone secretion |
| dc.description.none.fl_txt_mv |
Objective: Herpes simplex virus type 1 (HSV-1)-derived vectors are known to be effective tools to deliver transgenes into normal and neoplastic anterior pituitary (AP) cells <i>in vitro</i>. Our objective was to assess the <i>in vitro</i> and <i>in vivo</i> effects of tsK/β-gal, a temperature-sensitive HSV-1-derived vector harbouring the <i>E. coli</i> β-galactosidase gene, on AP hormone secretion as well as on transgene expression in rat AP tumours (hyperplastic prolactinomas). Design: The impact of vector infection on prolactin (PRL) and GH release was determined <i>in vitro</i> in normal and hyperplastic (lactotrophic) dispersed AP cells exposed for 24 h to tsK/β-gal as well as <i>in vivo</i> in ectopic AP grafts. In some oestrogen-induced prolactinoma-carrying rats, vector suspension was stereotaxically injected into the glands to assess transgene expression <i>in vivo</i>. Methods: GH and PRL release was measured by specific RIAs. <i>In vivo</i> transgene expression was assessed by immunohistochemistry for β-galactosidase and enzymohistochemistry (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside). Ectopic pituitary grafts and stereotaxic surgery were performed following standard procedures. Results: At a multiplicity of infection of 0.5, the vector induced a 30 and 22% fall in PRL and GH release respectively in normal AP cells, whereas the corresponding hormone release inhibition for hyperplastic AP cells was 41 and 33% for PRL and GH respectively. In ectopic pituitary grafts, the effect of vector infection on hormone secretion was assessed by measuring serum PRL levels in the host rats every 5 days for 4 weeks post-grafting. In the pituitary-grafted rats that received the viral vector, serum PRL failed to increase to the levels achieved in control-grafted animals. Finally, pituitary tumours stereotaxically injected with tsK/β-gal showed widespread expression of the β-galactosidase transgene around the injection areas. Conclusions: The results reported here have implications for basic studies using gene transfer to pituitary gland as well as potential gene therapy approaches to pituitary diseases. Instituto de Investigaciones Bioquímicas de La Plata Instituto de Biotecnologia y Biologia Molecular Instituto Multidisciplinario de Biología Celular |
| description |
Objective: Herpes simplex virus type 1 (HSV-1)-derived vectors are known to be effective tools to deliver transgenes into normal and neoplastic anterior pituitary (AP) cells <i>in vitro</i>. Our objective was to assess the <i>in vitro</i> and <i>in vivo</i> effects of tsK/β-gal, a temperature-sensitive HSV-1-derived vector harbouring the <i>E. coli</i> β-galactosidase gene, on AP hormone secretion as well as on transgene expression in rat AP tumours (hyperplastic prolactinomas). Design: The impact of vector infection on prolactin (PRL) and GH release was determined <i>in vitro</i> in normal and hyperplastic (lactotrophic) dispersed AP cells exposed for 24 h to tsK/β-gal as well as <i>in vivo</i> in ectopic AP grafts. In some oestrogen-induced prolactinoma-carrying rats, vector suspension was stereotaxically injected into the glands to assess transgene expression <i>in vivo</i>. Methods: GH and PRL release was measured by specific RIAs. <i>In vivo</i> transgene expression was assessed by immunohistochemistry for β-galactosidase and enzymohistochemistry (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside). Ectopic pituitary grafts and stereotaxic surgery were performed following standard procedures. Results: At a multiplicity of infection of 0.5, the vector induced a 30 and 22% fall in PRL and GH release respectively in normal AP cells, whereas the corresponding hormone release inhibition for hyperplastic AP cells was 41 and 33% for PRL and GH respectively. In ectopic pituitary grafts, the effect of vector infection on hormone secretion was assessed by measuring serum PRL levels in the host rats every 5 days for 4 weeks post-grafting. In the pituitary-grafted rats that received the viral vector, serum PRL failed to increase to the levels achieved in control-grafted animals. Finally, pituitary tumours stereotaxically injected with tsK/β-gal showed widespread expression of the β-galactosidase transgene around the injection areas. Conclusions: The results reported here have implications for basic studies using gene transfer to pituitary gland as well as potential gene therapy approaches to pituitary diseases. |
| publishDate |
2001 |
| dc.date.none.fl_str_mv |
2001 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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http://sedici.unlp.edu.ar/handle/10915/83484 |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/issn/0804-4643 info:eu-repo/semantics/altIdentifier/doi/10.1530/eje.0.1450497 |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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openAccess |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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