A tissue-engineered human trabecular meshwork hydrogel for advanced glaucoma disease modeling.


Journal

Experimental eye research
ISSN: 1096-0007
Titre abrégé: Exp Eye Res
Pays: England
ID NLM: 0370707

Informations de publication

Date de publication:
04 2021
Historique:
received: 12 08 2020
revised: 15 01 2021
accepted: 20 01 2021
pubmed: 1 2 2021
medline: 4 9 2021
entrez: 31 1 2021
Statut: ppublish

Résumé

Abnormal human trabecular meshwork (HTM) cell function and extracellular matrix (ECM) remodeling contribute to HTM stiffening in primary open-angle glaucoma (POAG). Most current cellular HTM model systems do not sufficiently replicate the complex native three dimensional (3D) cell-ECM interface, limiting their use for investigating POAG pathology. Tissue-engineered hydrogels are ideally positioned to overcome shortcomings of current models. Here, we report a novel biomimetic HTM hydrogel and test its utility as a POAG disease model. HTM hydrogels were engineered by mixing normal donor-derived HTM cells with collagen type I, elastin-like polypeptide and hyaluronic acid, each containing photoactive functional groups, followed by UV crosslinking. Glaucomatous conditions were induced with dexamethasone (DEX), and effects of the Rho-associated kinase (ROCK) inhibitor Y27632 on cytoskeletal organization and tissue-level function, contingent on HTM cell-ECM interactions, were assessed. DEX exposure increased HTM hydrogel contractility, f-actin and alpha smooth muscle actin abundance and rearrangement, ECM remodeling, and fibronectin deposition - all contributing to HTM hydrogel condensation and stiffening consistent with glaucomatous HTM tissue behavior. Y27632 treatment produced precisely the opposite effects and attenuated the DEX-induced pathologic changes, resulting in HTM hydrogel relaxation and softening. For model validation, confirmed glaucomatous HTM (GTM) cells were encapsulated; GTM hydrogels showed increased contractility, fibronectin deposition, and stiffening vs. normal HTM hydrogels despite reduced GTM cell proliferation. We have developed a biomimetic HTM hydrogel model for detailed investigation of 3D cell-ECM interactions under normal and simulated glaucomatous conditions. Its bidirectional responsiveness to pharmacological challenge and rescue suggests promising potential to serve as screening platform for new POAG treatments with focus on HTM biomechanics.

Identifiants

pubmed: 33516765
pii: S0014-4835(21)00037-3
doi: 10.1016/j.exer.2021.108472
pii:
doi:

Substances chimiques

Actins 0
Amides 0
Cytoskeletal Proteins 0
ELN protein, human 0
Enzyme Inhibitors 0
Eye Proteins 0
Glucocorticoids 0
Glycoproteins 0
Hydrogels 0
Pyridines 0
trabecular meshwork-induced glucocorticoid response protein 0
Y 27632 138381-45-0
Dexamethasone 7S5I7G3JQL
Elastin 9007-58-3
rho-Associated Kinases EC 2.7.11.1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108472

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Haiyan Li (H)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; BioInspired Institute, Syracuse University, Syracuse, NY, 13244, USA.

Tyler Bagué (T)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.

Alexander Kirschner (A)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.

Ana N Strat (AN)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.

Haven Roberts (H)

Duke Eye Center, Duke University, Durham, NC, 27708, USA.

Robert W Weisenthal (RW)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.

Alison E Patteson (AE)

BioInspired Institute, Syracuse University, Syracuse, NY, 13244, USA; Department of Physics, Syracuse University, Syracuse, NY, 13244, USA.

Nasim Annabi (N)

Department of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, CA, 90095, USA.

W Daniel Stamer (WD)

Duke Eye Center, Duke University, Durham, NC, 27708, USA.

Preethi S Ganapathy (PS)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; BioInspired Institute, Syracuse University, Syracuse, NY, 13244, USA; Department of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.

Samuel Herberg (S)

Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; BioInspired Institute, Syracuse University, Syracuse, NY, 13244, USA; Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; Department of Biomedical and Chemical Engineering, Syracuse University, Syracuse, NY, 13244, USA. Electronic address: herbergs@upstate.edu.

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Classifications MeSH