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Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes
The silk glands of silkworms produce large quantities of fibroin, which is a protein that can be physically processed and used as a biodegradable carrier for cell growth factors in tissue engineering applications. Meanwhile, protein microcrystals known as polyhedra, which are derived from cypovirus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734426/ https://www.ncbi.nlm.nih.gov/pubmed/33336160 http://dx.doi.org/10.1096/fba.2020-00078 |
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author | Maruta, Rina Takaki, Keiko Yamaji, Yuka Sezutsu, Hideki Mori, Hajime Kotani, Eiji |
author_facet | Maruta, Rina Takaki, Keiko Yamaji, Yuka Sezutsu, Hideki Mori, Hajime Kotani, Eiji |
author_sort | Maruta, Rina |
collection | PubMed |
description | The silk glands of silkworms produce large quantities of fibroin, which is a protein that can be physically processed and used as a biodegradable carrier for cell growth factors in tissue engineering applications. Meanwhile, protein microcrystals known as polyhedra, which are derived from cypovirus 1, have been used as a vehicle to protect and release encapsulated cell growth factors. We report the generation of transgenic silkworms that express recombinant fibroblast growth factor‐7 (FGF‐7) fused with the polyhedron‐encapsulating signal in polyhedra produced in the middle (MSG) and posterior (PSG) silk glands. Immunofluorescence showed that polyhedra from silk glands are associated with FGF‐7. The MSG and PSG from transgenic silkworms were processed into fine powdery materials, from which FGF‐7 activity was released to stimulate the proliferation of human keratinocyte epidermal cells. Powders from PSGs exhibited higher FGF‐7 activity than those from MSGs. Moreover, PSG powder showed a gradual release of FGF‐7 activity over a long period and induced keratinocyte proliferation and differentiation in 3D culture to promote the formation of stratified epidermis expressing positive differentiation marker proteins. Our results indicate that powdery materials incorporating the FGF‐7‐polyhedra microcrystals from silk glands are valuable for developing cell/tissue engineering applications in vivo and in vitro. |
format | Online Article Text |
id | pubmed-7734426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77344262020-12-16 Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes Maruta, Rina Takaki, Keiko Yamaji, Yuka Sezutsu, Hideki Mori, Hajime Kotani, Eiji FASEB Bioadv Research Articles The silk glands of silkworms produce large quantities of fibroin, which is a protein that can be physically processed and used as a biodegradable carrier for cell growth factors in tissue engineering applications. Meanwhile, protein microcrystals known as polyhedra, which are derived from cypovirus 1, have been used as a vehicle to protect and release encapsulated cell growth factors. We report the generation of transgenic silkworms that express recombinant fibroblast growth factor‐7 (FGF‐7) fused with the polyhedron‐encapsulating signal in polyhedra produced in the middle (MSG) and posterior (PSG) silk glands. Immunofluorescence showed that polyhedra from silk glands are associated with FGF‐7. The MSG and PSG from transgenic silkworms were processed into fine powdery materials, from which FGF‐7 activity was released to stimulate the proliferation of human keratinocyte epidermal cells. Powders from PSGs exhibited higher FGF‐7 activity than those from MSGs. Moreover, PSG powder showed a gradual release of FGF‐7 activity over a long period and induced keratinocyte proliferation and differentiation in 3D culture to promote the formation of stratified epidermis expressing positive differentiation marker proteins. Our results indicate that powdery materials incorporating the FGF‐7‐polyhedra microcrystals from silk glands are valuable for developing cell/tissue engineering applications in vivo and in vitro. John Wiley and Sons Inc. 2020-10-20 /pmc/articles/PMC7734426/ /pubmed/33336160 http://dx.doi.org/10.1096/fba.2020-00078 Text en © 2020 The Authors. FASEB BioAdvances published by the Federation of American Societies for Experimental Biology This is an open access article under the terms of the http://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 Maruta, Rina Takaki, Keiko Yamaji, Yuka Sezutsu, Hideki Mori, Hajime Kotani, Eiji Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title | Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title_full | Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title_fullStr | Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title_full_unstemmed | Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title_short | Effects of transgenic silk materials that incorporate FGF‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
title_sort | effects of transgenic silk materials that incorporate fgf‐7 protein microcrystals on the proliferation and differentiation of human keratinocytes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734426/ https://www.ncbi.nlm.nih.gov/pubmed/33336160 http://dx.doi.org/10.1096/fba.2020-00078 |
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