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Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells
Collagenous scaffolds provide good conditions for embryonic nerve cell growth. The aim of the current study was to assess the brains reaction to the implantation of 3D sponge-shaped scaffolds. These scaffolds consisted of collagen (Col) and Col with chondroitin sulphate, which is modified by carbodi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862020/ https://www.ncbi.nlm.nih.gov/pubmed/31772645 http://dx.doi.org/10.3892/etm.2019.8116 |
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author | Drobnik, Jacek Pietrucha, Krystyna Janczar, Karolina Polis, Lech Polis, Bartosz Safandowska, Marta Szymański, Jacek |
author_facet | Drobnik, Jacek Pietrucha, Krystyna Janczar, Karolina Polis, Lech Polis, Bartosz Safandowska, Marta Szymański, Jacek |
author_sort | Drobnik, Jacek |
collection | PubMed |
description | Collagenous scaffolds provide good conditions for embryonic nerve cell growth. The aim of the current study was to assess the brains reaction to the implantation of 3D sponge-shaped scaffolds. These scaffolds consisted of collagen (Col) and Col with chondroitin sulphate, which is modified by carbodiimide, or Col crosslinked with dialdehyde cellulose. The current study also evaluated the expression of integrins α2 and β1 in embryonic nerve cells. Embryonic nerve cells were isolated from the brains of rat embryos. Acellular scaffolds, or scaffolds populated with embryonic nerve cells, were implanted into the rats brain. The fibers of all the implanted scaffolds remained intact and served as a template for cell infiltration. The implants induced minimal to moderate inflammatory responses and minimal glial scar formations. Immunohistochemical studies did not indicate any microtubule-associated protein 2 or glial fibrillary acidic protein-positive cells inside the scaffolds. Acellular and cell-populated scaffolds yielded similar responses in the brain. The expression of integrin α2 and β1 was observed in embryonic nervous cells. TC-I15, the integrin α2β1 inhibitor, was not demonstrated to modify cell entrapment within the collagenous scaffolds. All applied scaffolds were well tolerated by the tissue and were indicated to support blood vessel formation. Therefore, all tested biomaterials are recommended for further studies. Additional chemical modifications of the material are suggested to protect the seeded cells from apoptosis after implantation into the brain. |
format | Online Article Text |
id | pubmed-6862020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-68620202019-11-26 Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells Drobnik, Jacek Pietrucha, Krystyna Janczar, Karolina Polis, Lech Polis, Bartosz Safandowska, Marta Szymański, Jacek Exp Ther Med Articles Collagenous scaffolds provide good conditions for embryonic nerve cell growth. The aim of the current study was to assess the brains reaction to the implantation of 3D sponge-shaped scaffolds. These scaffolds consisted of collagen (Col) and Col with chondroitin sulphate, which is modified by carbodiimide, or Col crosslinked with dialdehyde cellulose. The current study also evaluated the expression of integrins α2 and β1 in embryonic nerve cells. Embryonic nerve cells were isolated from the brains of rat embryos. Acellular scaffolds, or scaffolds populated with embryonic nerve cells, were implanted into the rats brain. The fibers of all the implanted scaffolds remained intact and served as a template for cell infiltration. The implants induced minimal to moderate inflammatory responses and minimal glial scar formations. Immunohistochemical studies did not indicate any microtubule-associated protein 2 or glial fibrillary acidic protein-positive cells inside the scaffolds. Acellular and cell-populated scaffolds yielded similar responses in the brain. The expression of integrin α2 and β1 was observed in embryonic nervous cells. TC-I15, the integrin α2β1 inhibitor, was not demonstrated to modify cell entrapment within the collagenous scaffolds. All applied scaffolds were well tolerated by the tissue and were indicated to support blood vessel formation. Therefore, all tested biomaterials are recommended for further studies. Additional chemical modifications of the material are suggested to protect the seeded cells from apoptosis after implantation into the brain. D.A. Spandidos 2019-12 2019-10-21 /pmc/articles/PMC6862020/ /pubmed/31772645 http://dx.doi.org/10.3892/etm.2019.8116 Text en Copyright: © Drobnik et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Drobnik, Jacek Pietrucha, Krystyna Janczar, Karolina Polis, Lech Polis, Bartosz Safandowska, Marta Szymański, Jacek Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title | Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title_full | Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title_fullStr | Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title_full_unstemmed | Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title_short | Intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
title_sort | intra-cerebral implantation of a variety of collagenous scaffolds with nervous embryonic cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6862020/ https://www.ncbi.nlm.nih.gov/pubmed/31772645 http://dx.doi.org/10.3892/etm.2019.8116 |
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