Evidence map›Paper›PMID 41251307›Full record

ArticleBiology open2025

Microtubule dependent changes in cell polarity are required for mammary epithelial cell migration and branching morphogenesis.

Andrew K Fraser, Joshua Carreras, Isabel A Ryan, Jennifer Zoll, Andrew J Ewald

Abstract read
In one paragraph

Article in Biology open, 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

5 authors.

Andrew K FraserDepartment of Cell Biology, Giovanis Institute of Translational Cell Biology, and Center for Cell Dynamics, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Joshua CarrerasDepartment of Cell Biology, Giovanis Institute of Translational Cell Biology, and Center for Cell Dynamics, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Isabel A RyanDepartment of Cell Biology, Giovanis Institute of Translational Cell Biology, and Center for Cell Dynamics, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Jennifer ZollDepartment of Cell Biology, Giovanis Institute of Translational Cell Biology, and Center for Cell Dynamics, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Andrew J EwaldDepartment of Cell Biology, Giovanis Institute of Translational Cell Biology, and Center for Cell Dynamics, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.

Funding

QAQC Johns Hopkins Institute for Clinical and Translational ResearchUL1TR003098 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2019 to 2023
$57.7M
Medical Scientist Training ProgramT32GM136577 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ANDREA L COX · 2020 to 2026
$13.4M
Tech Core 2U54CA268083 · NCI · JOHNS HOPKINS UNIVERSITY · PI Andrew Josef Ewald · 2022 to 2026
$10.2M
Mapping the single cell state basis of metastasis in space and timeU01CA284090 · NCI · JOHNS HOPKINS UNIVERSITY · PI Andrew Josef Ewald · 2023 to 2026
$2.7M
LSM880 Laser-scanning Microscope with Airyscan ModuleS10OD023548 · OD · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2018 to 2018
$439k
Breast Cancer Research Foundation BCRF-24-048Ewald Lab- JHUNational Science Foundation 1915491NCATS NIH HHS UL1 TR003098NCI NIH HHS U01 CA284090NCI NIH HHS U54 CA268083NCI NIH HHS U54CA268083NIGMS NIH HHS T32 GM136577NIH HHS S10 OD023548NIH HHS T32 GM136577
6 · The paper itself

Abstract

Branching morphogenesis requires dramatic changes in cell polarity, proliferation, migration, and actin dynamics to elaborate tubular networks. However, little is known about how microtubules support these cell behaviors in 3D tissues. Using organotypic cultures, we first examined the organization of the microtubule cytoskeleton. Simple luminal epithelial cells exhibited non-centrosomal, apico-basally oriented microtubule arrays, while stratified luminal cells had centrosomally radiating microtubules. During collective migration, luminal cells adopted an ameboid-like organization with a rear-facing nuclear-centrosomal axis. Multiple staining approaches suggest that cells in the basal-most luminal cell layer had more stable microtubules than cells deeper within the stratified layer. Finally, we tested the requirement for microtubules using pharmacologic inhibitors. Both microtubule stabilization and destabilization prevented bud formation and arrested duct elongation. Cell tracking analysis demonstrated that microtubules coordinated luminal cell migration within elongating buds. Destabilizing microtubules reduced cell directionality, while stabilizing microtubules did not affect directionality but reduced cell motility. Our data reveal that microtubules are essential for collective migration of luminal cells and for mammary branching morphogenesis.

Indexed as

Cell MovementCell PolarityEpithelial CellsMammary Glands, AnimalMicrotubulesMorphogenesisAnimalsFemaleHumansMammary Glands, HumanBranching morphogenesisMammary epitheliumMicrotubules

Identifiers

PMID41251307
PMCPMC12746711

What OpenQuestion holds

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LicenceCC BY
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.