Evidence map›Paper›PMID 42461077›Full record

ArticleInvestigative ophthalmology & visual science2026

Novel Role for CGRP in Aqueous Humor Outflow.

Timur A Mavlyutov, Samer E Bilal, Tania Sharmin, Colleen M McDowell

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
–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

4 authors.

Timur A MavlyutovDepartment of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison Wisconsin, United States.
Samer E BilalDepartment of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison Wisconsin, United States.
Tania SharminDepartment of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison Wisconsin, United States.
Colleen M McDowellDepartment of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison Wisconsin, United States.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
UW Vision Research Core - Administrative CoreP30EY016665 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI AKIHIRO IKEDA · 2005 to 2026
$12.6M
Waisman Center Intellectual and Developmental Disabilities Research CenterP50HD105353 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Qiang Chang · 2021 to 2026
$8.5M
Automated Tissue MicroarrayerS10OD023526 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI MATKOWSKYJ, KRISTINA A. · 2018 to 2018
$184k
NCI NIH HHS P30 CA014520NEI NIH HHS P30 EY016665NICHD NIH HHS P50 HD105353NIH HHS S10 OD023526
6 · The paper itself

Abstract

Purpose: Calcitonin gene related peptide (CGRP)-positive nerve fibers are the major type of sensory neurons innervating the trabecular meshwork (TM) and Schlemm's canal (SC). Upon activation, these neurons secrete CGRP locally. Here, we determined the role of CGRP in regulating homeostatic TM functions and the relation of CGRP-positive neurite innervation to segmental outflow regions. Methods: CGRP receptor expression in primary human TM (HTM) and primary human SC (HSC) cells in culture was determined by western blot analysis. HTM cells were treated with CGRP (0.1-3 µM) and fluorescent beads for 24 hours or were treated with CGRP (1 µM), TGFβ2 (5 ng/mL), and CGRP+TGFβ2 for 48 hours and processed for western blot analysis of alpha-smooth muscle actin (α-SMA) and collagen type 1 alpha 1 (COL1A1) expression. Segmental flow regions were determined in 9-month-old C57BL/6J mice using fluorescent tracer beads. Anterior segment flatmounts were co-labeled with antibodies against CGRP, CALCRL (CGRP receptor), and PECAM-1 (SC endothelium) and imaged by confocal microscopy. The density of CGRP neurites and CALCRL expression in each flow region were quantified by ImageJ analysis. Results: CGRP receptors are expressed in human TM and SC cells. CGRP treatment significantly increased phagocytosis and blocked TGFβ2-induced COL1A1 and α-SMA expression. Significantly more CGRP-positive neurites were identified in high-flow regions compared to all other flow regions. CALCRL expression was significantly associated with high-flow and moderate-flow regions compared to no-flow regions. Conclusions: These data suggest that CGRP modulates important homeostatic mechanisms of TM function and may influence the development and regulation of segmental regions of aqueous humor outflow.

Indexed as

Aqueous HumorCalcitonin Gene-Related PeptideSchlemm's CanalTrabecular MeshworkActinsAnimalsBlotting, WesternCells, CulturedCollagen Type IHumansMaleMiceMice, Inbred C57BLReceptors, Calcitonin Gene-Related PeptideActinsCalcitonin Gene-Related PeptideCollagen Type IReceptors, Calcitonin Gene-Related Peptide

Identifiers

PMID42461077
PMCPMC13387256

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.