Evidence map›Paper›PMID 42497164›Full record

ArticlePLoS biology2026

Cell type-specific Ca2+ signals govern mouse seminiferous tubule physiology.

Justine A Fischoeder, David Fleck, Jerome Schröer, Christopher Wiesbrock, Lina Kenzler, Christoph Weber-Hamacher, Ilian Schröder, Melissa Franke, Stefanie Kurth, Martin Strauch and 6 more

Abstract read
In one paragraph

Article in PLoS biology, 2026. 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

16 authors.

Justine A FischoederDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
David FleckDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Jerome SchröerDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Christopher WiesbrockDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Lina KenzlerDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Christoph Weber-HamacherDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Ilian SchröderDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Melissa FrankeDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Stefanie KurthDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Martin StrauchInstitute of Imaging and Computer Vision, RWTH Aachen University, Aachen, Germany.
Guiscard SeebohmDepartment of Cardiology and Angiology, University Hospital of Münster, Münster, Germany.
Dorit MerhofResearch Training Group 2416 MultiSenses - MultiScales, RWTH Aachen University, Aachen, Germany.
Johannes StegmaierCenter for Digital Medicine, Faculty of Mathematics and Natural Sciences, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Naofumi UesakaDepartment of Cognitive Neurobiology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, Japan.
Jennifer SpehrDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.
Marc SpehrDepartment of Chemosensation, Institute for Biology II, RWTH Aachen University, Aachen, Germany.ORCID https://orcid.org/0000-0001-6616-4196

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spermatogenesis, the complex developmental process of male germ cell proliferation, differentiation, and maturation, is the basis of male fertility. In the seminiferous tubules of the testes, spermatozoa are constantly generated from spermatogonial stem cells through a stereotyped sequence of divisions. The basic physiological principles, however, that control seminiferous tubule function remain poorly, if at all, defined. Here, we address cell type-specific seminiferous tubule signaling in vitro and in vivo. By monitoring changes in cellular Ca2+ concentration at high spatiotemporal resolution, we show that the three cell types that build the seminiferous epithelium-Sertoli, peritubular, and germ cells-each display unique Ca2+ signaling patterns. We reveal the underlying mechanisms and demonstrate that Sertoli cell Ca2+ signals are under gonadotropin regulation. Together, our experimental findings provide insights into seminiferous tubule signaling, its mechanistic basis, and its endocrine control.

Indexed as

Calcium SignalingSeminiferous TubulesAnimalsCalciumMaleMiceSertoli CellsSpermatogenesisSpermatozoaCalcium

Identifiers

PMID42497164
PMCPMC13399359

What OpenQuestion holds

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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.