Evidence map›Paper›PMID 38102391›Full record

ReviewNature reviews. Endocrinology2024

Pituitary stem cells: past, present and future perspectives.

María Inés Pérez Millán, Leonard Y M Cheung, Florencia Mercogliano, Maria Andrea Camilletti, Gonzalo T Chirino Felker, Lucia N Moro, Santiago Miriuka, Michelle L Brinkmeier, Sally A Camper

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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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

9 authors at 4 institutions in 2 countries.

María Inés Pérez MillánInstitute of Bioscience, Biotechnology and Translational Biology (IB3-UBA), University of Buenos Aires, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-0486-109X
Leonard Y M CheungDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-0912-9594
Florencia MercoglianoInstitute of Bioscience, Biotechnology and Translational Biology (IB3-UBA), University of Buenos Aires, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0003-1094-9247
Maria Andrea CamillettiInstitute of Bioscience, Biotechnology and Translational Biology (IB3-UBA), University of Buenos Aires, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-5160-5523
Gonzalo T Chirino FelkerLaboratory of Applied Research of Neurosciences (LIAN-CONICET), FLENI Sede Escobar, Buenos Aires, Argentina.ORCID http://orcid.org/0009-0002-0073-9983
Lucia N MoroLaboratory of Applied Research of Neurosciences (LIAN-CONICET), FLENI Sede Escobar, Buenos Aires, Argentina.ORCID http://orcid.org/0009-0004-2308-1381
Santiago MiriukaLaboratory of Applied Research of Neurosciences (LIAN-CONICET), FLENI Sede Escobar, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0003-2402-3920
Michelle L BrinkmeierDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0001-9505-4682
Sally A CamperDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA. scamper@umich.edu.ORCID http://orcid.org/0000-0001-8556-3379
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad de Buenos Aires · ARUniversity of Michigan · USState University of New York · US

Funding

Hypopituitarism: role of PROP1 and retinoic acid signaling in regulation of pituitary stem cell differentiationR01HD097096 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CAMPER, SALLY A. · 2019 to 2023
$2.2M
Fundamental Mechanisms Causing Pituitary Stem Cell Aging in Mice and HumansR03AG072221 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHEUNG, LEONARD YAN MING · 2022 to 2023
$157k
NIA NIH HHS R03 AG072221NICHD NIH HHS R01 HD097096
6 · The paper itself

Abstract

Pituitary cells that express the transcription factor SOX2 are stem cells because they can self-renew and differentiate into multiple pituitary hormone-producing cell types as organoids. Wounding and physiological challenges can activate pituitary stem cells, but cell numbers are not fully restored, and the ability to mobilize stem cells decreases with increasing age. The basis of these limitations is still unknown. The regulation of stem cell quiescence and activation involves many different signalling pathways, including those mediated by WNT, Hippo and several cytokines; more research is needed to understand the interactions between these pathways. Pituitary organoids can be formed from human or mouse embryonic stem cells, or from human induced pluripotent stem cells. Human pituitary organoid transplantation is sufficient to induce corticosterone release in hypophysectomized mice, raising the possibility of therapeutic applications. Today, pituitary organoids have the potential to assess the role of individual genes and genetic variants on hormone production ex vivo, providing an important tool for the advancement of exciting frontiers in pituitary stem cell biology and pituitary organogenesis. In this article, we provide an overview of notable discoveries in pituitary stem cell function and highlight important areas for future research.

Indexed as

Induced Pluripotent Stem CellsAnimalsCell DifferentiationHumansMicePituitary GlandSignal TransductionTranscription FactorsTranscription Factors

Identifiers

PMID38102391
PMCPMC10964491
OpenAlexW4389785602

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.