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Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells
BACKGROUND: In this study, 293T cells were genetically engineered to secrete tissue inhibitor of metalloproteinase-2 (TIMP2) and encapsulated into alginate microcapsules to continuously release TIMP2 protein. METHODS: The anti-invasive potential of the microcapsules was studied in vitro using brain...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826773/ https://www.ncbi.nlm.nih.gov/pubmed/24231999 http://dx.doi.org/10.2147/IJN.S52577 |
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author | Kim, Yeon Seong Jeong, Young-II Jin, Shu-Guang Pei, Jian Wen, Min Kim, In-Young Moon, Kyung-Sub Jung, Tae-Young Ryu, Hyang-Hwa Jung, Shin |
author_facet | Kim, Yeon Seong Jeong, Young-II Jin, Shu-Guang Pei, Jian Wen, Min Kim, In-Young Moon, Kyung-Sub Jung, Tae-Young Ryu, Hyang-Hwa Jung, Shin |
author_sort | Kim, Yeon Seong |
collection | PubMed |
description | BACKGROUND: In this study, 293T cells were genetically engineered to secrete tissue inhibitor of metalloproteinase-2 (TIMP2) and encapsulated into alginate microcapsules to continuously release TIMP2 protein. METHODS: The anti-invasive potential of the microcapsules was studied in vitro using brain tumor cells. The TIMP2 gene was transfected to 293T cells, and genetically engineered 293TIMP2 cells were encapsulated into alginate microcapsules. Release of TIMP2 protein was detected with Western blot analysis and the anti-invasive potential against U87MG cells was tested using gelatin zymography and a Matrigel assay. RESULTS: Cell viability within the alginate microcapsules was maintained at a cell density of 5 × 10(6). Because polycationic polymers are helpful for maintaining the mechanical strength of microcapsules with good cell viability, the alginate microcapsules were reinforced with chitosan (0.1% w/v). Expression of TIMP2 protein in cell lysates and secretion of TIMP2 into the conditioned medium was confirmed by Western blot analysis. Alginate microcapsules encapsulating 293TIMP2 cells released TIMP2 protein into the medium efficiently, where the TIMP2 protein participated in degradation of the matrix metalloproteinase-2 enzyme and inhibited invasion of U87MG cells. CONCLUSION: Alginate microcapsules encapsulating 293TIMP2 cells are promising candidates for anti-invasive treatment of glioma. |
format | Online Article Text |
id | pubmed-3826773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38267732013-11-14 Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells Kim, Yeon Seong Jeong, Young-II Jin, Shu-Guang Pei, Jian Wen, Min Kim, In-Young Moon, Kyung-Sub Jung, Tae-Young Ryu, Hyang-Hwa Jung, Shin Int J Nanomedicine Original Research BACKGROUND: In this study, 293T cells were genetically engineered to secrete tissue inhibitor of metalloproteinase-2 (TIMP2) and encapsulated into alginate microcapsules to continuously release TIMP2 protein. METHODS: The anti-invasive potential of the microcapsules was studied in vitro using brain tumor cells. The TIMP2 gene was transfected to 293T cells, and genetically engineered 293TIMP2 cells were encapsulated into alginate microcapsules. Release of TIMP2 protein was detected with Western blot analysis and the anti-invasive potential against U87MG cells was tested using gelatin zymography and a Matrigel assay. RESULTS: Cell viability within the alginate microcapsules was maintained at a cell density of 5 × 10(6). Because polycationic polymers are helpful for maintaining the mechanical strength of microcapsules with good cell viability, the alginate microcapsules were reinforced with chitosan (0.1% w/v). Expression of TIMP2 protein in cell lysates and secretion of TIMP2 into the conditioned medium was confirmed by Western blot analysis. Alginate microcapsules encapsulating 293TIMP2 cells released TIMP2 protein into the medium efficiently, where the TIMP2 protein participated in degradation of the matrix metalloproteinase-2 enzyme and inhibited invasion of U87MG cells. CONCLUSION: Alginate microcapsules encapsulating 293TIMP2 cells are promising candidates for anti-invasive treatment of glioma. Dove Medical Press 2013 2013-11-06 /pmc/articles/PMC3826773/ /pubmed/24231999 http://dx.doi.org/10.2147/IJN.S52577 Text en © 2013 Kim et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kim, Yeon Seong Jeong, Young-II Jin, Shu-Guang Pei, Jian Wen, Min Kim, In-Young Moon, Kyung-Sub Jung, Tae-Young Ryu, Hyang-Hwa Jung, Shin Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title | Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title_full | Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title_fullStr | Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title_full_unstemmed | Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title_short | Release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
title_sort | release of tissue inhibitor of metalloproteinase-2 from alginate microcapsule encapsulating genetically engineered cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826773/ https://www.ncbi.nlm.nih.gov/pubmed/24231999 http://dx.doi.org/10.2147/IJN.S52577 |
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