A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary
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Abstract
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 pituitaryspecific 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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Garcia-Lavandeira M, Quereda V, Flores I, Saez C, Diaz-Rodriguez E, Japon MA, et al. (2009) A GRFa2/Prop1/Stem (GPS) Cell Niche in the Pituitary. PLoS ONE 4(3): e4815. https://doi.org/10.1371/journal.pone.0004815
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https://doi.org/10.1371/journal.pone.0004815Sponsors
V.Q. was supported by a fellowship from the Spanish Ministry of Education and Science. This work was funded by grants from the Foundation of the
Asociacion Espanola contra el Cancer (AECC; to M.M.), Foundation Mutua Madrilena Automovilista (to M.M.), Xunta de Galicia PGIDIT05BTF20803PR (to C.V.A. and
C.D.) and the Ministry of Education and Science (MICINN; SAF2004-03131 and BFU2007-60571 to C.V.A. and SAF2006-05186, to M.M.). The Cell Division and Cancer
Group of the CNIO is supported by the OncoCycle programme from the Comunidad de Madrid (S-BIO-0283-2006) and the Consolider-Ingenio (CSD2007-00017)
program from the MICINN
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Copyright: © 2009 Garcia-Lavandeira et al. 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 credited








