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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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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. |
format | Online Article Text |
id | pubmed-7376689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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