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A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary

BACKGROUND: The adult endocrine pituitary is known to host several hormone-producing cells regulating major physiological processes during life. Some candidates to progenitor/stem cells have been proposed. However, not much is known about pituitary cell renewal throughout life and its homeostatic re...

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Autores principales: Garcia-Lavandeira, Montse, Quereda, Víctor, Flores, Ignacio, Saez, Carmen, Diaz-Rodriguez, Esther, Japon, Miguel A., Ryan, Aymee K., Blasco, Maria A., Dieguez, Carlos, Malumbres, Marcos, Alvarez, Clara V.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654029/
https://www.ncbi.nlm.nih.gov/pubmed/19283075
http://dx.doi.org/10.1371/journal.pone.0004815
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author Garcia-Lavandeira, Montse
Quereda, Víctor
Flores, Ignacio
Saez, Carmen
Diaz-Rodriguez, Esther
Japon, Miguel A.
Ryan, Aymee K.
Blasco, Maria A.
Dieguez, Carlos
Malumbres, Marcos
Alvarez, Clara V.
author_facet Garcia-Lavandeira, Montse
Quereda, Víctor
Flores, Ignacio
Saez, Carmen
Diaz-Rodriguez, Esther
Japon, Miguel A.
Ryan, Aymee K.
Blasco, Maria A.
Dieguez, Carlos
Malumbres, Marcos
Alvarez, Clara V.
author_sort Garcia-Lavandeira, Montse
collection PubMed
description BACKGROUND: The adult endocrine pituitary is known to host several hormone-producing cells regulating major physiological processes during life. Some candidates to progenitor/stem cells have been proposed. However, not much is known about pituitary cell renewal throughout life and its homeostatic regulation during specific physiological changes, such as puberty or pregnancy, or in pathological conditions such as tumor development. PRINCIPAL FINDINGS: We have identified in rodents and humans a niche of non-endocrine cells characterized by the expression of GFRa2, a Ret co-receptor for Neurturin. These cells also express b-Catenin and E-cadherin in an oriented manner suggesting a planar polarity organization for the niche. In addition, cells in the niche uniquely express the pituitary-specific transcription factor Prop1, as well as known progenitor/stem markers such as Sox2, Sox9 and Oct4. Half of these GPS (GFRa2/Prop1/Stem) cells express S-100 whereas surrounding elongated cells in contact with GPS cells express Vimentin. GFRa2+-cells form non-endocrine spheroids in culture. These spheroids can be differentiated to hormone-producing cells or neurons outlining the neuroectoderm potential of these progenitors. In vivo, GPSs cells display slow proliferation after birth, retain BrdU label and show long telomeres in its nuclei, indicating progenitor/stem cell properties in vivo. SIGNIFICANCE: Our results suggest the presence in the adult pituitary of a specific niche of cells characterized by the expression of GFRa2, the pituitary-specific protein Prop1 and stem cell markers. These GPS cells are able to produce different hormone-producing and neuron-like cells and they may therefore contribute to postnatal pituitary homeostasis. Indeed, the relative abundance of GPS numbers is altered in Cdk4-deficient mice, a model of hypopituitarism induced by the lack of this cyclin-dependent kinase. Thus, GPS cells may display functional relevance in the physiological expansion of the pituitary gland throughout life as well as protection from pituitary disease.
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spelling pubmed-26540292009-03-13 A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary Garcia-Lavandeira, Montse Quereda, Víctor Flores, Ignacio Saez, Carmen Diaz-Rodriguez, Esther Japon, Miguel A. Ryan, Aymee K. Blasco, Maria A. Dieguez, Carlos Malumbres, Marcos Alvarez, Clara V. PLoS One Research Article BACKGROUND: The adult endocrine pituitary is known to host several hormone-producing cells regulating major physiological processes during life. Some candidates to progenitor/stem cells have been proposed. However, not much is known about pituitary cell renewal throughout life and its homeostatic regulation during specific physiological changes, such as puberty or pregnancy, or in pathological conditions such as tumor development. PRINCIPAL FINDINGS: We have identified in rodents and humans a niche of non-endocrine cells characterized by the expression of GFRa2, a Ret co-receptor for Neurturin. These cells also express b-Catenin and E-cadherin in an oriented manner suggesting a planar polarity organization for the niche. In addition, cells in the niche uniquely express the pituitary-specific transcription factor Prop1, as well as known progenitor/stem markers such as Sox2, Sox9 and Oct4. Half of these GPS (GFRa2/Prop1/Stem) cells express S-100 whereas surrounding elongated cells in contact with GPS cells express Vimentin. GFRa2+-cells form non-endocrine spheroids in culture. These spheroids can be differentiated to hormone-producing cells or neurons outlining the neuroectoderm potential of these progenitors. In vivo, GPSs cells display slow proliferation after birth, retain BrdU label and show long telomeres in its nuclei, indicating progenitor/stem cell properties in vivo. SIGNIFICANCE: Our results suggest the presence in the adult pituitary of a specific niche of cells characterized by the expression of GFRa2, the pituitary-specific protein Prop1 and stem cell markers. These GPS cells are able to produce different hormone-producing and neuron-like cells and they may therefore contribute to postnatal pituitary homeostasis. Indeed, the relative abundance of GPS numbers is altered in Cdk4-deficient mice, a model of hypopituitarism induced by the lack of this cyclin-dependent kinase. Thus, GPS cells may display functional relevance in the physiological expansion of the pituitary gland throughout life as well as protection from pituitary disease. Public Library of Science 2009-03-13 /pmc/articles/PMC2654029/ /pubmed/19283075 http://dx.doi.org/10.1371/journal.pone.0004815 Text en Garcia-Lavandeira et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Garcia-Lavandeira, Montse
Quereda, Víctor
Flores, Ignacio
Saez, Carmen
Diaz-Rodriguez, Esther
Japon, Miguel A.
Ryan, Aymee K.
Blasco, Maria A.
Dieguez, Carlos
Malumbres, Marcos
Alvarez, Clara V.
A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title_full A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title_fullStr A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title_full_unstemmed A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title_short A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
title_sort grfa2/prop1/stem (gps) cell niche in the pituitary
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654029/
https://www.ncbi.nlm.nih.gov/pubmed/19283075
http://dx.doi.org/10.1371/journal.pone.0004815
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