Evidence map›Paper›PMID 40460128›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Single-cell resolution uncovers neighboring cell subtypes that share steroidogenic capacity during fetal testis development.

Keer Jiang, Zirui Fu, Philippos Tsourkas, Anbarasi Kothandapani, Tyler Kearse, Sean J McIlwain, Chloé Mayère, Serge Nef, Joan S Jorgensen

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Platelet-derived growth factor receptor alpha regulates fetal testis differentiation via an ERK-CREB axis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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.

Keer JiangDepartment of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706.ORCID 0000-0001-6260-3796
Zirui FuDepartment of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706.
Philippos TsourkasCancer Informatics Shared Resource, Carbone Cancer Center, University of Wisconsin, Madison, WI 53792.ORCID 0000-0002-0364-7040
Anbarasi KothandapaniDepartment of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706.
Tyler KearseDepartment of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706.
Sean J McIlwainCancer Informatics Shared Resource, Carbone Cancer Center, University of Wisconsin, Madison, WI 53792.
Chloé MayèreDepartment of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva 1211, Switzerland.ORCID 0000-0002-9254-4886
Serge NefDepartment of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva 1211, Switzerland.ORCID 0000-0001-5462-0676
Joan S JorgensenDepartment of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706.ORCID 0000-0002-5787-8856

Funding

WNPRC Supplemental Request for Nonhuman Primate Enclosures to Equip HIV/AIDS-Related Research FacilitiesP51OD011106 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI Dorota A. Grejner-Brzezinska · 2012 to 2026
$150.7M
UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Mediators for dynamic regulation of Star transcription in Leydig cellsR01HD090660 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI JEFCOATE, COLIN ROBERT, JORGENSEN, JOAN S · 2017 to 2021
$3.1M
Request for triple quadrupole mass spectrometer (LC-MS/MS) for biomarker analysisS10OD028626 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI KAPOOR, AMITA · 2020 to 2020
$313k
NCI NIH HHS P30 CA014520NICHD NIH HHS R01 HD090660NIH HHS P51 OD011106NIH HHS S10 OD028626
6 · The paper itself

Abstract

Historically, endocrine cells were perceived to coordinate their output in a uniform manner. Recently however, single-cell technologies have uncovered heterogeneity within these populations, indicating that individual cells may operate as independently regulated units. Using high-resolution tools such as single-molecule fluorescent in situ hybridization (sm-FISH) and single-cell RNA sequencing (scRNA-seq), we investigated the contributions of individual and the collective of fetal Leydig cells to androgen production over time during mouse testis development. Temporal profiles of intratesticular androgens alongside the expression of steroidogenic pathway genes (

Indexed as

AndrogensLeydig CellsSingle-Cell AnalysisTestisAnimalsFemaleFetusGene Expression Regulation, DevelopmentalIn Situ Hybridization, FluorescenceMaleMiceAndrogensfetal testisLeydig cellsteroidogenesistestosteronetranscription

Identifiers

PMID40460128
PMCPMC12167995

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.