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Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration
Corneal blindness is a worldwide major cause of vision loss, and corneal transplantation remains to be the most effective way to restore the vision. However, often there is a shortage of the donor corneas for transplantation. Therefore, it is urgent to develop a novel tissue‐engineered corneal subst...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354768/ https://www.ncbi.nlm.nih.gov/pubmed/37476050 http://dx.doi.org/10.1002/btm2.10531 |
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author | Kang, Honghua Han, Yi Jin, Mengyi Zheng, Lan Liu, Zhen Xue, Yuhua Liu, Zuguo Li, Cheng |
author_facet | Kang, Honghua Han, Yi Jin, Mengyi Zheng, Lan Liu, Zhen Xue, Yuhua Liu, Zuguo Li, Cheng |
author_sort | Kang, Honghua |
collection | PubMed |
description | Corneal blindness is a worldwide major cause of vision loss, and corneal transplantation remains to be the most effective way to restore the vision. However, often there is a shortage of the donor corneas for transplantation. Therefore, it is urgent to develop a novel tissue‐engineered corneal substitute. The present study envisaged the development of a novel and efficient method to prepare the corneal stromal equivalent from the marine biomaterials‐squid. A chemical method was employed to decellularize the squid mantle scaffold to create a cell‐free tissue substitute using 0.5% sodium dodecyl sulfate (SDS) solution. Subsequently, a novel clearing method, namely clear, unobstructed brain imaging cocktails (CUBIC) method was used to transparent it. Decellularized squid mantle scaffold (DSMS) has high decellularization efficiency, is rich in essential amino acids, and maintains the regular fiber alignment. In vitro experiments showed that the soaking solution of DSMS was non‐toxic to human corneal epithelium cells. DSMS exhibited a good biocompatibility in the rat muscle by undergoing a complete degradation, and promoted the growth of the muscle. In addition, the DSMS showed a good compatibility with the corneal stroma in the rabbit inter‐corneal implantation model, and promoted the regeneration of the corneal stroma without any evident rejection. Our results indicate that the squid mantle can be a potential new type of tissue‐engineered corneal stroma material with a promising clinical application. |
format | Online Article Text |
id | pubmed-10354768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103547682023-07-20 Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration Kang, Honghua Han, Yi Jin, Mengyi Zheng, Lan Liu, Zhen Xue, Yuhua Liu, Zuguo Li, Cheng Bioeng Transl Med Research Articles Corneal blindness is a worldwide major cause of vision loss, and corneal transplantation remains to be the most effective way to restore the vision. However, often there is a shortage of the donor corneas for transplantation. Therefore, it is urgent to develop a novel tissue‐engineered corneal substitute. The present study envisaged the development of a novel and efficient method to prepare the corneal stromal equivalent from the marine biomaterials‐squid. A chemical method was employed to decellularize the squid mantle scaffold to create a cell‐free tissue substitute using 0.5% sodium dodecyl sulfate (SDS) solution. Subsequently, a novel clearing method, namely clear, unobstructed brain imaging cocktails (CUBIC) method was used to transparent it. Decellularized squid mantle scaffold (DSMS) has high decellularization efficiency, is rich in essential amino acids, and maintains the regular fiber alignment. In vitro experiments showed that the soaking solution of DSMS was non‐toxic to human corneal epithelium cells. DSMS exhibited a good biocompatibility in the rat muscle by undergoing a complete degradation, and promoted the growth of the muscle. In addition, the DSMS showed a good compatibility with the corneal stroma in the rabbit inter‐corneal implantation model, and promoted the regeneration of the corneal stroma without any evident rejection. Our results indicate that the squid mantle can be a potential new type of tissue‐engineered corneal stroma material with a promising clinical application. John Wiley & Sons, Inc. 2023-05-09 /pmc/articles/PMC10354768/ /pubmed/37476050 http://dx.doi.org/10.1002/btm2.10531 Text en © 2023 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Kang, Honghua Han, Yi Jin, Mengyi Zheng, Lan Liu, Zhen Xue, Yuhua Liu, Zuguo Li, Cheng Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title | Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title_full | Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title_fullStr | Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title_full_unstemmed | Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title_short | Decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
title_sort | decellularized squid mantle scaffolds as tissue‐engineered corneal stroma for promoting corneal regeneration |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354768/ https://www.ncbi.nlm.nih.gov/pubmed/37476050 http://dx.doi.org/10.1002/btm2.10531 |
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