Evidence map›Paper›PMID 41002216›Full record

ReviewToxicological sciences : an official journal of the Society of Toxicology2025

In vitro models of the male reproductive system: applications for developmental and reproductive toxicology.

Brad C Hansen, Kayenat S Aryeh, Lillian X Lindell, Gabriel K Lau, Tristan M Nicholson, Elaine M Faustman, Edward J Kelly

Abstract readReview
In one paragraph

Review in Toxicological sciences : an official journal of the Society of Toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Brad C HansenDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, United States.ORCID 0000-0003-1524-0878
Kayenat S AryehDepartment of Pharmaceutics, University of Washington, Seattle, WA 98105, United States.
Lillian X LindellDepartment of Urology, University of Washington, Seattle, WA 98105, United States.
Gabriel K LauDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, United States.
Tristan M NicholsonDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, United States.
Elaine M FaustmanDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, United States.ORCID 0000-0002-3085-6403
Edward J KellyInstitute for Stem Cells and Regenerative Medicine, University of Washington, Seattle, WA 98105, United States.ORCID 0000-0002-6534-9313

Funding

Environmetal Pathology/Toxicology Training ProgramT32ES007032 · NIEHS · UNIVERSITY OF WASHINGTON · PI FAUSTMAN, ELAINE M, ROSENFELD, MICHAEL E · 1985 to 2023
$10.7M
University of Washington Pediatric and Reproductive Environmental Health Scholars (UW PREHS)K12ES033584 · NIEHS · UNIVERSITY OF WASHINGTON · PI CATHERINE J KARR, Sheela Sathyanarayana · 2022 to 2026
$2.4M
NIEHS NIH HHS K12 ES033584NIEHS NIH HHS T32 ES007032University of Washington Institute of Stem Cells and Regenerative Medicine Fellowship
6 · The paper itself

Abstract

There is a paucity of in vitro models to study the male reproductive system. Proper function of the reproductive system is critical for endocrine function, growth and development, and fertility. Without practical in vitro screening models, reproductive toxicities can be missed in early drug development or standard toxicological batteries. Successful in vitro models of the male reproductive system need to recapitulate the dynamic nature of the testis, considering the formation of the testicular niches from gonadal differentiation through puberty and the post-pubertal activity of the paracrine and endocrine signals that support spermatogenesis. In vitro approaches are reviewed that model primordial germ cell differentiation, gonadal morphogenesis, fetal steroidogenesis, neonatal reproductive development, and adult testicular niche dynamics to present opportunities for inclusion of male reproductive toxicity screening within a toxicological battery. The utility of cells derived from model organisms, differentiated from induced pluripotent stem cells, and obtained from donated human tissue is discussed. The field of reproductive and developmental toxicology is primed for expansion in in-vitro model availability as complex in-vitro model development continues to accelerate, and fit-for-purpose model approaches are adopted in toxicological and drug development pipelines. This review highlights the current limitations and emerging opportunities in male reproductive in vitro models, providing a roadmap for integrating these systems into toxicology testing and drug development workflows. It highlights the need for developmentally benchmarked, physiologically relevant, and multicellular models to fill existing gaps and improve translatability.

Indexed as

Genitalia, MaleModels, BiologicalReproductionTestisToxicity TestsAnimalsCell DifferentiationHumansMaledevelopmental toxicityin vitro modelsmale reproductive toxicitytestis

Identifiers

PMID41002216
PMCPMC13397029

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.