All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors
- Autores
- Davis, Shannon W.; Keisler, Jessica L.; Pérez Millán, María Inés; Schade, Vanessa; Camper, Sally A.
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mutations in PROP1, the most common known cause of combined pituitary hormone deficiency in humans, can result in the progressive loss of all hormones of the pituitary anterior lobe. In mice, Prop1 mutations result in the failure to initiate transcription of Pou1f1 (also known as Pit1) and lack somatotropins, lactotropins, and thyrotropins. The basis for this species difference is unknown. We hypothesized that Prop1 is expressed in a progenitor cell that can develop into all anterior lobe cell types, and not just the somatotropes, thyrotropes, and lactotropes, which are collectively known as the PIT1 lineage. To test this idea, we produced a transgenic Prop1-cre mouse line and conducted lineage-tracing experiments of Prop1-expressing cells. The results reveal that all hormone-secreting cell types of both the anterior and intermediate lobes are descended from Prop1-expressing progenitors. The Prop1-cre mice also provide a valuable genetic reagent with a unique spatial and temporal expression for generating tissue-specific gene rearrangements early in pituitary gland development. We also determined that the minimal essential sequences for reliable Prop1 expression lie within 10 kilobases of the mouse gene and demonstrated that human PROP1 can substitute functionally for mouse Prop1. These studies enhance our understanding of the pathophysiology of disease in patients with PROP1 mutations.
Fil: Davis, Shannon W.. University of South Carolina; Estados Unidos
Fil: Keisler, Jessica L.. University of South Carolina; Estados Unidos
Fil: Pérez Millán, María Inés. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Schade, Vanessa. University of Michigan; Estados Unidos
Fil: Camper, Sally A.. University of Michigan; Estados Unidos - Materia
-
Prop1
Pituitary
Stem Cells
Cre - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/39001
Ver los metadatos del registro completo
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spelling |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitorsDavis, Shannon W.Keisler, Jessica L.Pérez Millán, María InésSchade, VanessaCamper, Sally A.Prop1PituitaryStem CellsCrehttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Mutations in PROP1, the most common known cause of combined pituitary hormone deficiency in humans, can result in the progressive loss of all hormones of the pituitary anterior lobe. In mice, Prop1 mutations result in the failure to initiate transcription of Pou1f1 (also known as Pit1) and lack somatotropins, lactotropins, and thyrotropins. The basis for this species difference is unknown. We hypothesized that Prop1 is expressed in a progenitor cell that can develop into all anterior lobe cell types, and not just the somatotropes, thyrotropes, and lactotropes, which are collectively known as the PIT1 lineage. To test this idea, we produced a transgenic Prop1-cre mouse line and conducted lineage-tracing experiments of Prop1-expressing cells. The results reveal that all hormone-secreting cell types of both the anterior and intermediate lobes are descended from Prop1-expressing progenitors. The Prop1-cre mice also provide a valuable genetic reagent with a unique spatial and temporal expression for generating tissue-specific gene rearrangements early in pituitary gland development. We also determined that the minimal essential sequences for reliable Prop1 expression lie within 10 kilobases of the mouse gene and demonstrated that human PROP1 can substitute functionally for mouse Prop1. These studies enhance our understanding of the pathophysiology of disease in patients with PROP1 mutations.Fil: Davis, Shannon W.. University of South Carolina; Estados UnidosFil: Keisler, Jessica L.. University of South Carolina; Estados UnidosFil: Pérez Millán, María Inés. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Schade, Vanessa. University of Michigan; Estados UnidosFil: Camper, Sally A.. University of Michigan; Estados UnidosEndocrine Society2016-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/39001Davis, Shannon W.; Keisler, Jessica L.; Pérez Millán, María Inés; Schade, Vanessa; Camper, Sally A.; All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors; Endocrine Society; Endocrinology; 157; 4; 4-2016; 1385-13960013-7227CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1210/en.2015-1862info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article/157/4/1385/2422446info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:56:05Zoai:ri.conicet.gov.ar:11336/39001instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:56:05.867CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
title |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
spellingShingle |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors Davis, Shannon W. Prop1 Pituitary Stem Cells Cre |
title_short |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
title_full |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
title_fullStr |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
title_full_unstemmed |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
title_sort |
All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors |
dc.creator.none.fl_str_mv |
Davis, Shannon W. Keisler, Jessica L. Pérez Millán, María Inés Schade, Vanessa Camper, Sally A. |
author |
Davis, Shannon W. |
author_facet |
Davis, Shannon W. Keisler, Jessica L. Pérez Millán, María Inés Schade, Vanessa Camper, Sally A. |
author_role |
author |
author2 |
Keisler, Jessica L. Pérez Millán, María Inés Schade, Vanessa Camper, Sally A. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Prop1 Pituitary Stem Cells Cre |
topic |
Prop1 Pituitary Stem Cells Cre |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Mutations in PROP1, the most common known cause of combined pituitary hormone deficiency in humans, can result in the progressive loss of all hormones of the pituitary anterior lobe. In mice, Prop1 mutations result in the failure to initiate transcription of Pou1f1 (also known as Pit1) and lack somatotropins, lactotropins, and thyrotropins. The basis for this species difference is unknown. We hypothesized that Prop1 is expressed in a progenitor cell that can develop into all anterior lobe cell types, and not just the somatotropes, thyrotropes, and lactotropes, which are collectively known as the PIT1 lineage. To test this idea, we produced a transgenic Prop1-cre mouse line and conducted lineage-tracing experiments of Prop1-expressing cells. The results reveal that all hormone-secreting cell types of both the anterior and intermediate lobes are descended from Prop1-expressing progenitors. The Prop1-cre mice also provide a valuable genetic reagent with a unique spatial and temporal expression for generating tissue-specific gene rearrangements early in pituitary gland development. We also determined that the minimal essential sequences for reliable Prop1 expression lie within 10 kilobases of the mouse gene and demonstrated that human PROP1 can substitute functionally for mouse Prop1. These studies enhance our understanding of the pathophysiology of disease in patients with PROP1 mutations. Fil: Davis, Shannon W.. University of South Carolina; Estados Unidos Fil: Keisler, Jessica L.. University of South Carolina; Estados Unidos Fil: Pérez Millán, María Inés. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Schade, Vanessa. University of Michigan; Estados Unidos Fil: Camper, Sally A.. University of Michigan; Estados Unidos |
description |
Mutations in PROP1, the most common known cause of combined pituitary hormone deficiency in humans, can result in the progressive loss of all hormones of the pituitary anterior lobe. In mice, Prop1 mutations result in the failure to initiate transcription of Pou1f1 (also known as Pit1) and lack somatotropins, lactotropins, and thyrotropins. The basis for this species difference is unknown. We hypothesized that Prop1 is expressed in a progenitor cell that can develop into all anterior lobe cell types, and not just the somatotropes, thyrotropes, and lactotropes, which are collectively known as the PIT1 lineage. To test this idea, we produced a transgenic Prop1-cre mouse line and conducted lineage-tracing experiments of Prop1-expressing cells. The results reveal that all hormone-secreting cell types of both the anterior and intermediate lobes are descended from Prop1-expressing progenitors. The Prop1-cre mice also provide a valuable genetic reagent with a unique spatial and temporal expression for generating tissue-specific gene rearrangements early in pituitary gland development. We also determined that the minimal essential sequences for reliable Prop1 expression lie within 10 kilobases of the mouse gene and demonstrated that human PROP1 can substitute functionally for mouse Prop1. These studies enhance our understanding of the pathophysiology of disease in patients with PROP1 mutations. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-04 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/11336/39001 Davis, Shannon W.; Keisler, Jessica L.; Pérez Millán, María Inés; Schade, Vanessa; Camper, Sally A.; All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors; Endocrine Society; Endocrinology; 157; 4; 4-2016; 1385-1396 0013-7227 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/39001 |
identifier_str_mv |
Davis, Shannon W.; Keisler, Jessica L.; Pérez Millán, María Inés; Schade, Vanessa; Camper, Sally A.; All hormone-producing cell types of the pituitary intermediate and anterior lobes derive from prop1-expressing progenitors; Endocrine Society; Endocrinology; 157; 4; 4-2016; 1385-1396 0013-7227 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1210/en.2015-1862 info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article/157/4/1385/2422446 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Endocrine Society |
publisher.none.fl_str_mv |
Endocrine Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846083096747704320 |
score |
12.891075 |