Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions
In the search of biomaterials that promote cell adhesion, it is crucial to explore the integrin-substrate dynamic interactions given in a certain cell type to design successful biofunctionalization strategies. Here, we use a microarray platform for a thorough characterization of cell adhesion to a p...
| Autores: | , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Universidad del País Vasco |
| Repositorio: | Addi. Archivo Digital para la Docencia y la Investigación |
| OAI Identifier: | oai:addi.ehu.eus:10810/36386 |
| Acceso en línea: | http://hdl.handle.net/10810/36386 |
| Access Level: | acceso abierto |
| Palabra clave: | integrin ECM cell therapy biosensor biomaterial single cell array |
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Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactionsGonzález Pujana, AinhoaSantos Vizcaíno, EdortaGarcía Hernando, MaiteHernáez Estrada, BeatrizMartínez de Pancorbo Gómez, María de los AngelesBenito López, FernandoIgartua Olaechea, ManuelaBasabe Desmonts, LourdesHernández Martín, Rosa MaríaintegrinECMcell therapybiosensorbiomaterialsingle cell arrayIn the search of biomaterials that promote cell adhesion, it is crucial to explore the integrin-substrate dynamic interactions given in a certain cell type to design successful biofunctionalization strategies. Here, we use a microarray platform for a thorough characterization of cell adhesion to a particular substrate. A biosensor based on an array of 20 μm fibronectin circular isles was adapted to tissue culture treated plates to facilitate the performance of cell adhesion assays and the posterior affinity analyses. This sensitive analytical tool enables not only the evaluation of the cell adhesion kinetics, but also the integrin profiling and their contribution to cell attachment and adhesion strengthening via clustering. In particular, the biosensor was able to detect a significantly slower adhesion kinetics in fibroblasts, namely Baby Hamster Kidney Fibroblasts (BHK) and Human Dermal Fibroblasts (hDF), in comparison to other cell types such as C2C12 Mouse Myoblasts (C2C12) or Human Mesenchymal Stem Cells (hMSCa). When directly comparing hDF and hMSCa, the analysis determined that the differing kinetics were caused by a distinct integrin expression profile. Whereas β1 presenting integrins were the major responsible for hDF attachment, hMSCa adherence was importantly dependent on β1 but also on other integrin classes. Additionally, results revealed that concerning cell adhesion consolidation, in hMSCa, both αvβ3 and β1-subunit-presenting integrins contributed similarly; whereas in hDF, the latter played a more important role. Hence, our biosensor provided crucial information for the development of new cell-adhesive biomaterials, which are key in multiple biomedical fields including cell therapy or tissue engineering.SAF2017-82292-R and BIO2016- 80417-P (MINECO/AEI/FEDER, UE), ICTS “NANBIOSIS” (Drug Formulation Unit, U10) and the support from the Basque Country Government (Grupos Consolidados, No ref: IT907-16, IT127119). Basque Government (Department of Education, Universities and Research) for the PhD grant (PRE_2018_2_0133). University of the Basque Country for the PhD grant(PIF16/204). Basque Government for the PhD grant (PRE_2018_2_300).Elsevier201920192019info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10810/36386reponame:Addi. Archivo Digital para la Docencia y la Investigacióninstname:Universidad del País VascoInglésinfo:eu-repo/grantAgreement/MINECO/SAF2017-82292-R/info:eu-repo/grantAgreement/MINECO/BIO2016-80417-P/https://www.sciencedirect.com/science/article/pii/S0925400519311530info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/3.0/es/© 2019 Elsevieroai:addi.ehu.eus:10810/363862026-06-18T09:23:17Z |
| dc.title.none.fl_str_mv |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| title |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| spellingShingle |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions González Pujana, Ainhoa integrin ECM cell therapy biosensor biomaterial single cell array |
| title_short |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| title_full |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| title_fullStr |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| title_full_unstemmed |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| title_sort |
Extracellular matrix protein microarray-based biosensor with single cell resolution: Integrin profiling and characterization of cell-biomaterial interactions |
| dc.creator.none.fl_str_mv |
González Pujana, Ainhoa Santos Vizcaíno, Edorta García Hernando, Maite Hernáez Estrada, Beatriz Martínez de Pancorbo Gómez, María de los Angeles Benito López, Fernando Igartua Olaechea, Manuela Basabe Desmonts, Lourdes Hernández Martín, Rosa María |
| author |
González Pujana, Ainhoa |
| author_facet |
González Pujana, Ainhoa Santos Vizcaíno, Edorta García Hernando, Maite Hernáez Estrada, Beatriz Martínez de Pancorbo Gómez, María de los Angeles Benito López, Fernando Igartua Olaechea, Manuela Basabe Desmonts, Lourdes Hernández Martín, Rosa María |
| author_role |
author |
| author2 |
Santos Vizcaíno, Edorta García Hernando, Maite Hernáez Estrada, Beatriz Martínez de Pancorbo Gómez, María de los Angeles Benito López, Fernando Igartua Olaechea, Manuela Basabe Desmonts, Lourdes Hernández Martín, Rosa María |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
integrin ECM cell therapy biosensor biomaterial single cell array |
| topic |
integrin ECM cell therapy biosensor biomaterial single cell array |
| description |
In the search of biomaterials that promote cell adhesion, it is crucial to explore the integrin-substrate dynamic interactions given in a certain cell type to design successful biofunctionalization strategies. Here, we use a microarray platform for a thorough characterization of cell adhesion to a particular substrate. A biosensor based on an array of 20 μm fibronectin circular isles was adapted to tissue culture treated plates to facilitate the performance of cell adhesion assays and the posterior affinity analyses. This sensitive analytical tool enables not only the evaluation of the cell adhesion kinetics, but also the integrin profiling and their contribution to cell attachment and adhesion strengthening via clustering. In particular, the biosensor was able to detect a significantly slower adhesion kinetics in fibroblasts, namely Baby Hamster Kidney Fibroblasts (BHK) and Human Dermal Fibroblasts (hDF), in comparison to other cell types such as C2C12 Mouse Myoblasts (C2C12) or Human Mesenchymal Stem Cells (hMSCa). When directly comparing hDF and hMSCa, the analysis determined that the differing kinetics were caused by a distinct integrin expression profile. Whereas β1 presenting integrins were the major responsible for hDF attachment, hMSCa adherence was importantly dependent on β1 but also on other integrin classes. Additionally, results revealed that concerning cell adhesion consolidation, in hMSCa, both αvβ3 and β1-subunit-presenting integrins contributed similarly; whereas in hDF, the latter played a more important role. Hence, our biosensor provided crucial information for the development of new cell-adhesive biomaterials, which are key in multiple biomedical fields including cell therapy or tissue engineering. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019 2019 2019 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10810/36386 |
| url |
http://hdl.handle.net/10810/36386 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
info:eu-repo/grantAgreement/MINECO/SAF2017-82292-R/ info:eu-repo/grantAgreement/MINECO/BIO2016-80417-P/ https://www.sciencedirect.com/science/article/pii/S0925400519311530 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/3.0/es/ © 2019 Elsevier |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/3.0/es/ © 2019 Elsevier |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Elsevier |
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Elsevier |
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reponame:Addi. Archivo Digital para la Docencia y la Investigación instname:Universidad del País Vasco |
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Universidad del País Vasco |
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Addi. Archivo Digital para la Docencia y la Investigación |
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Addi. Archivo Digital para la Docencia y la Investigación |
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