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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
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.
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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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