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Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization

[Image: see text] Herein, we proposed a drug-free strategy named cell surface shellization to inhibit the motility of SKOV-3 and HeLa cells. We alternately deposited two- or three-layer cationic polyelectrolyte (PE) and anionic PE films on the surface of SKOV-3 and HeLa cells. Then, a mineral shell...

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Autores principales: Wei, Yan, Xu, Hao, Xu, Shuangmeng, Su, Hui, Zhang, Lichuang, Sun, Ruize, Huang, Di, Zhao, Liqin, Wang, Kaiqun, Hu, Yinchun, Lian, Xiaojie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376689/
https://www.ncbi.nlm.nih.gov/pubmed/32715197
http://dx.doi.org/10.1021/acsomega.0c00846
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author Wei, Yan
Xu, Hao
Xu, Shuangmeng
Su, Hui
Zhang, Lichuang
Sun, Ruize
Huang, Di
Zhao, Liqin
Wang, Kaiqun
Hu, Yinchun
Lian, Xiaojie
author_facet Wei, Yan
Xu, Hao
Xu, Shuangmeng
Su, Hui
Zhang, Lichuang
Sun, Ruize
Huang, Di
Zhao, Liqin
Wang, Kaiqun
Hu, Yinchun
Lian, Xiaojie
author_sort Wei, Yan
collection PubMed
description [Image: see text] Herein, we proposed a drug-free strategy named cell surface shellization to inhibit the motility of SKOV-3 and HeLa cells. We alternately deposited two- or three-layer cationic polyelectrolyte (PE) and anionic PE films on the surface of SKOV-3 and HeLa cells. Then, a mineral shell (calcium carbonate, CaCO(3)) was formed on the surface of polymer shells via electrostatic force and biomineralization. The CCK-8 assay results and live/dead staining showed that the surface shells strongly aggravated the cytotoxicity. The monolayer scratch wound migration assay results and immunofluorescence staining results showed that the shells, especially the mineral shells, could efficiently inhibit the migration of SKOV-3 and HeLa cells without any anticancer drugs. The immunofluorescence results of the three small G proteins of the cells showed that the immunofluorescence intensity in SKOV-3 did not change. Preliminary results from our laboratory showed an increase in MMP-9 secreted by cancer cells after coating with films or mineral shells. It suggests that mechanisms that inhibit cell migration are related to the MMP signaling pathway. All the results indicated that shellization (films or nanomineral shells) but not limited to calcification can be used as one of the tools to change the function of cells.
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spelling pubmed-73766892020-07-24 Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization Wei, Yan Xu, Hao Xu, Shuangmeng Su, Hui Zhang, Lichuang Sun, Ruize Huang, Di Zhao, Liqin Wang, Kaiqun Hu, Yinchun Lian, Xiaojie ACS Omega [Image: see text] Herein, we proposed a drug-free strategy named cell surface shellization to inhibit the motility of SKOV-3 and HeLa cells. We alternately deposited two- or three-layer cationic polyelectrolyte (PE) and anionic PE films on the surface of SKOV-3 and HeLa cells. Then, a mineral shell (calcium carbonate, CaCO(3)) was formed on the surface of polymer shells via electrostatic force and biomineralization. The CCK-8 assay results and live/dead staining showed that the surface shells strongly aggravated the cytotoxicity. The monolayer scratch wound migration assay results and immunofluorescence staining results showed that the shells, especially the mineral shells, could efficiently inhibit the migration of SKOV-3 and HeLa cells without any anticancer drugs. The immunofluorescence results of the three small G proteins of the cells showed that the immunofluorescence intensity in SKOV-3 did not change. Preliminary results from our laboratory showed an increase in MMP-9 secreted by cancer cells after coating with films or mineral shells. It suggests that mechanisms that inhibit cell migration are related to the MMP signaling pathway. All the results indicated that shellization (films or nanomineral shells) but not limited to calcification can be used as one of the tools to change the function of cells. American Chemical Society 2020-07-10 /pmc/articles/PMC7376689/ /pubmed/32715197 http://dx.doi.org/10.1021/acsomega.0c00846 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Wei, Yan
Xu, Hao
Xu, Shuangmeng
Su, Hui
Zhang, Lichuang
Sun, Ruize
Huang, Di
Zhao, Liqin
Wang, Kaiqun
Hu, Yinchun
Lian, Xiaojie
Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title_full Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title_fullStr Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title_full_unstemmed Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title_short Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization
title_sort inhibiting cell viability and motility by layer-by-layer assembly and biomineralization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376689/
https://www.ncbi.nlm.nih.gov/pubmed/32715197
http://dx.doi.org/10.1021/acsomega.0c00846
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