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
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/83484

id SEDICI_59a88f0f16de9be30dab39e74929d31a
oai_identifier_str oai:sedici.unlp.edu.ar:10915/83484
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling 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
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/10915/83484
url http://sedici.unlp.edu.ar/handle/10915/83484
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0804-4643
info:eu-repo/semantics/altIdentifier/doi/10.1530/eje.0.1450497
dc.rights.none.fl_str_mv 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)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
497-503
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
_version_ 1846064133883035648
score 13.22299