Evidence map›Paper›PMID 25917826›Full record

ArticleNature communications2015

Lineage specification of ovarian theca cells requires multicellular interactions via oocyte and granulosa cells.

Chang Liu, Jia Peng, Martin M Matzuk, Humphrey H-C Yao

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

123 citing papers in PubMed, 248 citations in OpenAlex.

  1. Spatiotemporally primed coelomic epithelium and supporting-like cells establish the dual origin of granulosa cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  11. Building a resilient ovarian reserve: Early soma-oocyte interactions.Current topics in developmental biology · 2026
    Review
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63 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

4 authors at 3 institutions in 1 country.

Chang Liu1] Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana Illinois, USA [2] Reproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, Durham, North Carolina, USA.
Jia Peng1] Departments of Pathology &Immunology, and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA [2] Centers for Drug Discovery and Reproductive Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
Martin M Matzuk1] Departments of Pathology &Immunology, and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA [2] Centers for Drug Discovery and Reproductive Medicine, Baylor College of Medicine, Houston, Texas 77030, USA [3] Departments of Molecular &Cellular Biology and Pharmacology, Baylor College of Medicine, Houston, Texas 77030, USA.
Humphrey H-C YaoReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, Durham, North Carolina, USA.
Baylor College of Medicine · USNational Institute of Environmental Health Sciences · USUniversity of Illinois Urbana-Champaign · US

Funding

Impacts of Genetic and Environmental Factors on Reproductive Organ DevelopmentZIAES102965 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI YAO, HUMPHREY · 2011 to 2025
$32.8M
Gene Expression and MicroarraysZICES102445 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI GERRISH, KEVIN · 2009 to 2025
$31.6M
REPRODUCTIVE FUNCTION USING TRANSGENIC MICER01HD033438 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MATZUK, MARTIN M. · 1996 to 2015
$2.5M
Intramural NIH HHS Z99 ES999999Intramural NIH HHS ZIA ES102965NICHD NIH HHS R01 HD033438NIEHS NIH HHS ES102965
6 · The paper itself

Abstract

Organogenesis of the ovary is a highly orchestrated process involving multiple lineage determination of ovarian surface epithelium, granulosa cells and theca cells. Although the sources of ovarian surface epithelium and granulosa cells are known, the origin(s) of theca progenitor cells have not been definitively identified. Here we show that theca cells derive from two sources: Wt1(+) cells indigenous to the ovary and Gli1(+) mesenchymal cells that migrate from the mesonephros. These progenitors acquire theca lineage marker Gli1 in response to paracrine signals Desert hedgehog (Dhh) and Indian hedgehog (Ihh) from granulosa cells. Ovaries lacking Dhh/Ihh exhibit theca layer loss, blunted steroid production, arrested folliculogenesis and failure to form corpora lutea. Production of Dhh/Ihh in granulosa cells requires growth differentiation factor 9 (GDF9) from the oocyte. Our studies provide the first genetic evidence for the origins of theca cells and reveal a multicellular interaction critical for the formation of a functional theca.

Indexed as

Theca CellsAnimalsCell DifferentiationCell LineageFemaleGranulosa CellsGrowth Differentiation Factor 9Hedgehog ProteinsKruppel-Like Transcription FactorsMaleMesonephrosMiceOocytesOrgan Culture TechniquesOvaryRepressor ProteinsGdf9 protein, mouseGli1 protein, mouseGrowth Differentiation Factor 9Hedgehog ProteinsKruppel-Like Transcription FactorsRepressor ProteinsWT1 protein, mouseWT1 ProteinsZinc Finger Protein GLI1

Identifiers

PMID25917826
PMCPMC4413950
OpenAlexW2055911575

What OpenQuestion holds

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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 OpenQuestion graph.