Evidence map›Paper›PMID 42360097›Full record

ArticleInvestigative ophthalmology & visual science2026

Comprehensive, High-Spatiotemporal-Resolution Intravital Two-Photon Imaging of the Mouse Conventional Outflow Pathway: Green Intravital Imaging.

Yui Urahashi, Yuji Takihara, Takumi Higaki, Takefumi Shimoda, Sachi Kojima, Mitsuhiro Endoh, Yuichiro Arima, Tomokazu Fujimoto, Norika Liu, Anna Irie and 3 more

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 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
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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

13 authors.

Yui UrahashiDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Yuji TakiharaDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takumi HigakiGraduate School of Science and Technology, Kumamoto University, Kumamoto, Japan.
Takefumi ShimodaDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Sachi KojimaDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Mitsuhiro EndohDepartment of Pluripotent Stem Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan.
Yuichiro ArimaDepartment of Anatomy, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Tomokazu FujimotoDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Norika LiuInternational Research Center for Medical Sciences, Kumamoto University, Kumamoto, Japan.
Anna IrieDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takahiro WatanabeDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Teruhiko HamanakaDepartment of Ophthalmology, Japanese Red Cross Medical Center, Tokyo, Japan.
Toshihiro InoueDepartment of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To develop an intravital imaging method that comprehensively shows the mouse conventional outflow pathway at high spatiotemporal resolution and to investigate the fine structures and dynamics within this pathway. Methods: Intravital two-photon imaging was performed using Green, Prox1-reporter, and mito-Dendra2 mice. Schlemm's canal (SC) in human patients with glaucoma was histologically evaluated. Results: The intravital two-photon imaging of Green mice ubiquitously expressing enhanced green fluorescent protein (EGFP) ("Green intravital imaging") demonstrated the perilimbal vein (PLV), collector channels (CCs), SC, and trabecular meshwork with and without a coverslip. A wide, tubular structure with septa was identified as SC in Prox1-reporter mice. Structures reminiscent of giant vacuoles and EGFP-positive vesicle flow were observed within SC. Based on the vesicle size, mitochondria in the vesicles, and platelet-specific intravital imaging findings, these EGFP-positive vesicles were identified as platelets. Moreover, platelet flow from the PLV into SC and from SC back to the PLV via CCs, as well as fast aqueous humor flow converging toward CCs, was observed. The quantitative analysis results suggested differences in aqueous flow velocity and flow patterns within SC. Platelets were also observed in SC of patients with glaucoma. Conclusions: Green intravital imaging comprehensively showed the proximal and distal conventional outflow pathway in mice at submicrometer spatial and 64.9-ms/frame temporal resolution, allowing observation of structures reminiscent of giant vacuoles. A subset of platelets transiently entered and exited SC via CCs. Within SC, aqueous humor exhibited fast flow converging toward the CCs, with differences in flow velocity and patterns. CCs may be involved in the heterogeneous dynamics of the aqueous humor.

Indexed as

Aqueous HumorGlaucomaIntravital MicroscopyMicroscopy, Fluorescence, MultiphotonSchlemm's CanalTrabecular MeshworkAnimalsDisease Models, AnimalGreen Fluorescent ProteinsHumansIntraocular PressureMiceMice, Inbred C57BLMice, Transgenicenhanced green fluorescent proteinGreen Fluorescent Proteins

Identifiers

PMID42360097
PMCPMC13317927

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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.