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An in vitro 3-dimensional Collagen-based Corneal Construct with Innervation Using Human Corneal Cell Lines.
Islam, Mohammad Mirazul; Saha, Amrita; Trisha, Farzana Afrose; Gonzalez-Andrades, Miguel; Patra, Hirak K; Griffith, May; Chodosh, James; Rajaiya, Jaya.
Affiliation
  • Islam MM; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear and Schepens Eye Research Institute, Boston, Massachusetts.
  • Saha A; Department of Ophthalmology and Visual Sciences, University of New Mexico School of Medicine, Albuquerque, New Mexico.
  • Trisha FA; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear and Schepens Eye Research Institute, Boston, Massachusetts.
  • Gonzalez-Andrades M; Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, Albuquerque, New Mexico.
  • Patra HK; Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear and Schepens Eye Research Institute, Boston, Massachusetts.
  • Griffith M; Department of Ophthalmology, Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofia University Hospital and University of Cordoba, Cordoba, Spain.
  • Chodosh J; UCL Division of Surgery and Interventional Science, Department of Surgical Biotechnology, University College London, London, UK.
  • Rajaiya J; Department of Ophthalmology, Université de Montréal and Centre de recherche de l'Hôpital Maisonneuve Rosemont, Montreal, Quebec, Canada.
Ophthalmol Sci ; 4(6): 100544, 2024.
Article in En | MEDLINE | ID: mdl-39139547
ABSTRACT

Purpose:

To develop a 3-dimensional corneal construct suitable for in vitro studies of disease conditions and therapies.

Design:

In vitro human corneal constructs were created using chemically crosslinked collagen and chondroitin sulfate extracellular matrix and seeded with 3 human corneal cell types (epithelial, stromal, and endothelial) together with neural cells. The neural cells were derived from hybrid neuroblastoma cells and the other cells used from immortalized human corneal cell lines. To check the feasibility and characterize the constructs, cytotoxicity, cell proliferation, histology, and protein expression studies were performed.

Results:

Optimized culture condition permitted synchronized viability across the cell types within the construct. The construct showed a typical appearance for different cellular layers, including healthy appearing, phenotypically differentiated neurons. The expected protein expression profiles for specific cell types within the construct were confirmed with western blotting.

Conclusions:

An in vitro corneal construct was successfully developed with maintenance of individual cell phenotypes with anatomically correct cellular loci. The construct may be useful in evaluation of specific corneal disorders and in developing different corneal disease models. Additionally, the construct can be used in evaluating drug targeting and/or penetration to individual corneal layers, testing novel therapeutics for corneal diseases, and potentially reducing the necessity for animals in corneal research at the early stages of investigation. Financial Disclosures Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Sci / Ophthalmology science Year: 2024 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Sci / Ophthalmology science Year: 2024 Document type: Article Country of publication: Netherlands