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Prevention of Corneal Myofibroblastic Differentiation In Vitro Using a Biomimetic ECM Hydrogel for Corneal Tissue Regeneration.
Chameettachal, Shibu; Prasad, Deeksha; Parekh, Yash; Basu, Sayan; Singh, Vivek; Bokara, Kiran Kumar; Pati, Falguni.
Afiliação
  • Chameettachal S; Department of Biomedical Engineering, Indian Institute of Technology Hyderabad, Kandi, Sangareddy 502285, Telangana, India.
  • Prasad D; SSR-Stem Cell Biology Laboratory, Center for Regenerative Ophthalmology, L V Prasad Eye Institute, Hyderabad 500034, Telangana, India.
  • Parekh Y; CSIR-Centre for Cellular and Molecular Biology, ANNEXE II, Medical Biotechnology Complex, Uppal Road, Hyderabad 500007, Telangana, India.
  • Basu S; SSR-Stem Cell Biology Laboratory, Center for Regenerative Ophthalmology, L V Prasad Eye Institute, Hyderabad 500034, Telangana, India.
  • Singh V; Centre for Ocular Regeneration (CORE), L V Prasad Eye Institute, Hyderabad 500034, Telangana, India.
  • Bokara KK; SSR-Stem Cell Biology Laboratory, Center for Regenerative Ophthalmology, L V Prasad Eye Institute, Hyderabad 500034, Telangana, India.
  • Pati F; Centre for Ocular Regeneration (CORE), L V Prasad Eye Institute, Hyderabad 500034, Telangana, India.
ACS Appl Bio Mater ; 4(1): 533-544, 2021 01 18.
Article em En | MEDLINE | ID: mdl-35014304
Corneal scarring is one of the major causes of blindness, affecting millions worldwide. Despite recent advancements in surgical strategies, there is an unmet need for a clinically feasible material and methods to prevent scarring following corneal injury. In this study, we report the potential utility of a hydrogel derived from cadaveric animal corneas, using a decellularized corneal matrix hydrogel (abbreviated as dCMH), which is prepared by a simple method. This hydrogel is easily injectable, biocompatible, and has the ability to maintain good shape-retention properties at 37 °C, which make it suitable for in vivo applications. Furthermore, our gene expression studies and immunofluorescence studies indicate that dCMH maintains the morphology and function of keratocytes in vitro and prevents their transdifferentiation to myofibroblasts. From the above results, it is evident that dCMH maintains the keratocytes with the ability to regenerate the corneal defect without scar. We thus suggest a simple yet effective approach for corneal tissue decellularization and that dCMH can be a promising material for prophylaxis against blinding scar formation in an injured cornea.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Hidrogéis / Matriz Extracelular Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Hidrogéis / Matriz Extracelular Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article