Effect of Rho-associated kinase inhibitor on human corneal endothelial cell apoptosis.
Adult
Aged
Amides
/ pharmacology
Annexin A5
/ metabolism
Antigens, CD
/ metabolism
Apoptosis
/ drug effects
Cell Adhesion Molecules, Neuronal
/ metabolism
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Cells, Cultured
Culture Media
Endothelium, Corneal
/ drug effects
Enzyme Inhibitors
/ pharmacology
Female
Fetal Proteins
/ metabolism
Flow Cytometry
Humans
Male
Middle Aged
Pyridines
/ pharmacology
Tissue Donors
rho-Associated Kinases
/ antagonists & inhibitors
Journal
Journal of cataract and refractive surgery
ISSN: 1873-4502
Titre abrégé: J Cataract Refract Surg
Pays: United States
ID NLM: 8604171
Informations de publication
Date de publication:
04 2020
04 2020
Historique:
pubmed:
23
2
2020
medline:
20
3
2021
entrez:
22
2
2020
Statut:
ppublish
Résumé
To evaluate whether exposure to Rho-associated protein kinase (ROCK) inhibitor will promote human-cultured corneal endothelial cells (CECs) survival in a commercial storage medium. Edith Wolfson Medical Center, Holon, and Sheba Medical Center, Tel Hashomer, Israel. Experimental study. Fragments of human donor corneolimbal rings were stored in commercial storage media for 1 week, half with the addition of 10 μM ROCK inhibitor (Y-27632). Evaluation of CECs for early and late apoptosis\necrosis rates was performed using anti-human CD166 antibody and flow cytometric double staining analysis of propidium iodide and Annexin V. CECs of 6 corneolimbal rings demonstrated a reduced early apoptosis rate (4.35% ± 1.07% vs 12.18% ± 5.5%, P = .026) and a reduced late apoptosis\necrosis rate (5.5% ± 2.39% vs 9.43% ± 2.61%, P = .004) compared with control. Subsequently, the rate of apoptotic CECs expressing ROCK was significantly lower in cells exposed to ROCK inhibitor compared with cells that were not (19.01% ± 4.17 vs 30.42% ± 4.27, P < .001). ROCK inhibitor reduced endothelial cell loss in vitro and might be used to limit or slow CEC loss in donor corneal tissue during eye banking. This might be a promising new method for promoting future graft survival.
Identifiants
pubmed: 32079844
doi: 10.1097/j.jcrs.0000000000000115
doi:
Substances chimiques
ALCAM protein, human
0
Amides
0
Annexin A5
0
Antigens, CD
0
Cell Adhesion Molecules, Neuronal
0
Culture Media
0
Enzyme Inhibitors
0
Fetal Proteins
0
Pyridines
0
Y 27632
138381-45-0
rho-Associated Kinases
EC 2.7.11.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM