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Multifunctional synthetic Bowman's membrane-stromal biomimetic for corneal reconstruction.
Wang, Xiaokun; Majumdar, Shoumyo; Soiberman, Uri; Webb, Joshua N; Chung, Liam; Scarcelli, Giuliano; Elisseeff, Jennifer H.
Afiliação
  • Wang X; Translational Tissue Engineering Center, Wilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, MD, USA.
  • Majumdar S; Translational Tissue Engineering Center, Wilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, MD, USA.
  • Soiberman U; Department of Ophthalmology, Johns Hopkins Hospital, Baltimore, MD, USA.
  • Webb JN; A. James Clark School of Bioengineering, University of Maryland, College Park, MD, USA.
  • Chung L; Translational Tissue Engineering Center, Wilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, MD, USA.
  • Scarcelli G; A. James Clark School of Bioengineering, University of Maryland, College Park, MD, USA.
  • Elisseeff JH; Translational Tissue Engineering Center, Wilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, MD, USA. Electronic address: jhe@jhu.edu.
Biomaterials ; 241: 119880, 2020 05.
Article em En | MEDLINE | ID: mdl-32097748
As the outermost layer of the eye, the cornea is vulnerable to physical and chemical trauma, which can result in loss of transparency and lead to corneal blindness. Given the global corneal donor shortage, there is an unmet need for biocompatible corneal substitutes that have high transparency, mechanical integrity and regenerative potentials. Herein we engineered a dual-layered collagen vitrigel containing biomimetic synthetic Bowman's membrane (sBM) and stromal layer (sSL). The sBM supported rapid epithelial cell migration, maturation and multilayer formation, and the sSL containing tissue-derived extracellular matrix (ECM) microparticles presented a biomimetic lamellar ultrastructure mimicking the native corneal stroma. The incorporation of tissue-derived microparticles in sSL layer significantly enhanced the mechanical properties and suturability of the implant without compromising the transparency after vitrification. In vivo performance of the vitrigel in a rabbit anterior lamellar keratoplasty model showed full re-epithelialization within 14 days and integration of the vitrigel with the host tissue stroma by day 30. The migrated epithelial cells formed functional multilayer with limbal stem cell marker p63 K14 expressed in the lower layer, epithelial marker K3 and K12 expressed through the layers and tight junction protein ZO-1 expressed by the multilayers. Corneal fibroblasts migrated into the implants to facilitate host/implant integration and corneal stromal regeneration. In summary, these results suggest that the multi-functional layers of this novel collagen vitrigel exhibited significantly improved biological performance as corneal substitute by harnessing a fast re-epithelialization and stromal regeneration potential.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Córnea / Lâmina Limitante Anterior Limite: Animals Idioma: En Revista: Biomaterials Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Córnea / Lâmina Limitante Anterior Limite: Animals Idioma: En Revista: Biomaterials Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos