Evidence map›Paper›PMID 19283075›Full record

ArticlePloS one2009

A GRFa2/Prop1/stem (GPS) cell niche in the pituitary.

Montse Garcia-Lavandeira, Víctor Quereda, Ignacio Flores, Carmen Saez, Esther Diaz-Rodriguez, Miguel A Japon, Aymee K Ryan, Maria A Blasco, Carlos Dieguez, Marcos Malumbres and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 183 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Pituitary Tumorigenesis-Implications for Management.Medicina (Kaunas, Lithuania) · 2023
    Review
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  11. Article
  12. Article
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  14. Article
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Montse Garcia-LavandeiraDepartment of Physiology, School of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
Víctor Quereda
Ignacio Flores
Carmen Saez
Esther Diaz-Rodriguez
Miguel A Japon
Aymee K Ryan
Maria A Blasco
Carlos Dieguez
Marcos Malumbres
Clara V Alvarez
Spanish National Cancer Research Centre · ESUniversidade de Santiago de Compostela · ESHospital Universitario Virgen del Rocío · ESInstituto de Salud Carlos III · ESMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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

findingsWe 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.

Indexed as

AnimalsBromodeoxyuridineCell ProliferationGene ExpressionGlial Cell Line-Derived Neurotrophic Factor ReceptorsHomeodomain ProteinsHumansHypopituitarismMiceOctamer Transcription Factor-3Pituitary GlandPituitary HormonesRatsStage-Specific Embryonic AntigensStem Cell NicheStem CellsBromodeoxyuridineGFRA2 protein, humanGlial Cell Line-Derived Neurotrophic Factor ReceptorsHomeodomain ProteinsOctamer Transcription Factor-3Pituitary HormonesProphet of Pit-1 proteinstage-specific embryonic antigen-4Stage-Specific Embryonic AntigensTranscription Factors

Identifiers

PMID19283075
PMCPMC2654029
OpenAlexW2023443384

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.