Evidence map›Paper›PMID 41928932›Full record

ArticlebioRxiv : the preprint server for biology2026

PRINCIPLES GOVERNING ENDOTHELIAL CAVEOLAE ORGANIZATION DURING ANGIOGENESIS.

Drew B Grespin, Jasper S Farrington, Talen G Niven, Liam J Russell, Dinah Loerke, Aaryn J David, Margaret S Grespin, Chris M Culkin, Adella P Bartoletti, Stryder M Meadows and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for 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

11 authors.

Drew B GrespinDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Jasper S FarringtonDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Talen G NivenDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Liam J RussellMolecular and Cellular Biophysics Programs, University of Denver, CO, USA.
Dinah LoerkeDepartment of Physics and Astronomy, University of Denver, CO, USA.
Aaryn J DavidDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Margaret S GrespinDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Chris M CulkinDepartment of Biological Sciences, University of Denver, Denver, CO, USA.
Adella P BartolettiCell and Molecular Biology Department, Tulane University, New Orleans, LA, USA.
Stryder M MeadowsCell and Molecular Biology Department, Tulane University, New Orleans, LA, USA.ORCID 0000-0003-0968-7155
Erich J KushnerDepartment of Biological Sciences, University of Denver, Denver, CO, USA.

Funding

Polarized Protein Trafficking and AngiogenesisR01HL155921 · NHLBI · UNIVERSITY OF DENVER (COLORADO SEMINARY) · PI Erich J Kushner · 2022 to 2026
$1.8M
120 kV Transmission Electron Microscope for CU Anschutz Electron Microscopy Core FacilityS10OD036258 · OD · UNIVERSITY OF COLORADO DENVER · PI FARHANG DAREHSHOURI, ANZA · 2024 to 2024
$678k
NHLBI NIH HHS R01 HL155921NIH HHS S10 OD036258
6 · The paper itself

Abstract

Caveolae, flask-shaped membrane invaginations highly enriched in endothelial cells, play a central role in buffering membrane tension, yet the principles governing their spatial organization remain elusive. This investigation sought to generate the most comprehensive and systematic analysis of blood vessel caveolar spatial organization. To do so, our group leveraged micropatterning technologies to impose precise biophysical constraints on endothelial cell geometry to probe how caveolae are organized under defined tensional and polarity environments. These experiments were integrated with a high-throughput spatial cell mapping computational pipeline for analyzing thousands of caveolae, providing an extremely high-fidelity analysis. Our results provide a governing framework of how total cellular caveolae are spatially organized during random and directional migration, non-motile polarized, nascent and stable monolayers with differing confinement levels as well as in angiogenic vasculature in vivo. Broadly, our results demonstrated caveolae preferentially organized in the rear of migrating and polarized endothelial cells. In differing monolayer configurations, caveolae default to a peri-junctional spatial organization. Lastly, in mouse retinal blood vessels caveolae are most prominent in the vascular front due to their responsiveness to vascular endothelial growth factor signaling. Overall, these results strongly suggest that caveolae cellular arrangement and number are highly predictive of vascular stability and remodeling states.

Indexed as

angiogenesisblood vesselscaveolaecaveolin 1cell culturecell migrationcomputational analysisdevelopmentEndothelial cellsmicropatterns

Identifiers

PMID41928932
PMCPMC13042058

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.