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Related Concept Videos

Open Angle Glaucoma: Treatment01:27

Open Angle Glaucoma: Treatment

477
In open-angle glaucoma, the iridocorneal angle remains open, but the trabecular meshwork becomes stiff, slowing down the outflow of aqueous humor. This causes a buildup of aqueous humor in the anterior chamber, leading to a sudden increase in intraocular pressure. The treatment for open-angle glaucoma focuses on reducing the elevated intraocular pressure by either decreasing the secretion of aqueous humor or increasing its outflow.
Drugs such as carbonic anhydrase inhibitors, α2- and...
477

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Updated: Jul 16, 2025

Trabecular Meshwork Response to Pressure Elevation in the Living Human Eye
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Nanofibrous PCL-Based Human Trabecular Meshwork for Aqueous Humor Outflow Studies.

Maria Bikuna-Izagirre1,2, Javier Aldazabal1,2,3, Leire Extramiana4

  • 1University of Navarra, TECNUN School of Engineering, Manuel Lardizabal 13, 20018 San Sebastián, Spain.

ACS Biomaterials Science & Engineering
|September 19, 2023
PubMed
Summary
This summary is machine-generated.

Researchers developed a novel in vitro model of the human trabecular meshwork (HTM) juxtacanalicular tissue (JCT) using a polycaprolactone scaffold. This model aids in studying aqueous humor outflow and human trabecular meshwork degeneration for glaucoma research.

Keywords:
drug screeningelectrospinningglaucomaoutflow systempolycaprolactonetrabecular meshwork

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Area of Science:

  • Biomedical Engineering
  • Ophthalmology
  • Cell Biology

Background:

  • Primary open-angle glaucoma involves optic nerve degeneration, with high intraocular pressure (IOP) as a key risk factor.
  • The human trabecular meshwork (HTM), particularly the juxtacanalicular tissue (JCT), regulates aqueous humor (AH) outflow and IOP.
  • Current in vitro JCT models are limited, hindering research into AH outflow and HTM degeneration.

Purpose of the Study:

  • To develop a functional in vitro JCT model using a polycaprolactone (PCL) nanofibrous scaffold.
  • To investigate the morphology, cell behavior, and drug responsiveness within the engineered JCT model.
  • To provide a platform for studying HTM cell biology and screening drugs affecting trabecular outflow.

Main Methods:

  • Fabrication of a PCL nanofibrous scaffold for JCT recapitulation.
  • Seeding human trabecular meshwork cells onto the scaffold.
  • Characterization using SEM, qPCR, and immunochemistry for HTM markers.
  • Construction of a pressure-sensitive perfusion system to assess outflow facility.
  • Testing drug responsiveness with dexamethasone and netarsudil.

Main Results:

  • The PCL scaffold supported HTM cell morphology and function, mimicking the JCT.
  • Engineered JCT exhibited characteristic HTM cell markers (myocilin, fibronectin, collagen IV) and genetic expression.
  • The model demonstrated functional outflow characteristics and responsiveness to IOP-lowering drugs.
  • Successful recapitulation of HTM cell biology and drug effects in vitro.

Conclusions:

  • A novel, functional in vitro JCT model was successfully developed using PCL nanofibrous scaffolds.
  • This model effectively mimics key aspects of the human JCT, including cell morphology, marker expression, and drug response.
  • The developed model serves as a valuable tool for understanding HTM cell biology, AH outflow regulation, and for pharmaceutical drug screening in glaucoma research.