A tissue-engineered human trabecular meshwork hydrogel for advanced glaucoma disease modeling.
Actins
/ metabolism
Aged, 80 and over
Amides
/ pharmacology
Biomimetic Materials
Cytoskeletal Proteins
/ genetics
Dexamethasone
/ pharmacology
Elastin
/ genetics
Enzyme Inhibitors
/ pharmacology
Eye Proteins
/ genetics
Female
Gene Expression Regulation
/ physiology
Glaucoma, Open-Angle
/ metabolism
Glucocorticoids
/ pharmacology
Glycoproteins
/ genetics
Humans
Hydrogels
Immunohistochemistry
Models, Biological
Pyridines
/ pharmacology
Real-Time Polymerase Chain Reaction
Tissue Engineering
Trabecular Meshwork
/ drug effects
rho-Associated Kinases
/ antagonists & inhibitors
Bioengineering
ECM mechanics
In vitro
POAG
Tissue stiffening
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
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
108472Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.