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The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation

Purpose: Stem cells can exhibit restorative effects with the commitment to functional cells.Cell-imprinted topographies provide adaptable templates and certain dimensions for thedifferentiation and bioactivity of stem cells. Cell sheet technology using the thermo-responsivepolymers detaches the &quo...

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Autores principales: Keyhanvar, Neda, Zarghami, Nosratollah, Seifalian, Alexander, Keyhanvar, Peyman, Sarvari, Rana, Salehi, Roya, Rahbarghazi, Reza, Ranjkesh, Mohammadreza, Akbarzadeh, Molood, Mahdipour, Mahdi, Nouri, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106954/
https://www.ncbi.nlm.nih.gov/pubmed/35620328
http://dx.doi.org/10.34172/apb.2022.034
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author Keyhanvar, Neda
Zarghami, Nosratollah
Seifalian, Alexander
Keyhanvar, Peyman
Sarvari, Rana
Salehi, Roya
Rahbarghazi, Reza
Ranjkesh, Mohammadreza
Akbarzadeh, Molood
Mahdipour, Mahdi
Nouri, Mohammad
author_facet Keyhanvar, Neda
Zarghami, Nosratollah
Seifalian, Alexander
Keyhanvar, Peyman
Sarvari, Rana
Salehi, Roya
Rahbarghazi, Reza
Ranjkesh, Mohammadreza
Akbarzadeh, Molood
Mahdipour, Mahdi
Nouri, Mohammad
author_sort Keyhanvar, Neda
collection PubMed
description Purpose: Stem cells can exhibit restorative effects with the commitment to functional cells.Cell-imprinted topographies provide adaptable templates and certain dimensions for thedifferentiation and bioactivity of stem cells. Cell sheet technology using the thermo-responsivepolymers detaches the "cell sheets" easier with less destructive effects on the extracellularmatrix (ECM). Here, we aim to dictate keratinocyte-like differentiation of mesenchymal stemcells (MSCs) by using combined cell imprinting and sheet technology. Methods: We developed the poly dimethyl siloxane (PDMS) substrate having keratinocytecell-imprinted topography grafted with the PNIPAAm polymer. Adipose tissue-derived MSCs(AT-MSCs) were cultured on PDMS substrate for 14 days and keratinocyte-like differentiationmonitored via the expression of involucrin, P63, and cytokeratin 14. Results: Data showed the efficiency of the current protocol in the fabrication of PDMSmolds. The culture of AT-MSCs induced typical keratinocyte morphology and up-regulatedthe expression of cytokeratin-14, Involucrin, and P63 compared to AT-MSCs cultured on theplastic surface (P < 0.05). Besides, KLC sheets were generated once slight changes occur in theenvironment temperature. Conclusion: These data showed the hypothesis that keratinocyte cell imprinted substrate canorient AT-MSCs toward KLCs by providing a specific niche and topography.
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spelling pubmed-91069542022-05-25 The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation Keyhanvar, Neda Zarghami, Nosratollah Seifalian, Alexander Keyhanvar, Peyman Sarvari, Rana Salehi, Roya Rahbarghazi, Reza Ranjkesh, Mohammadreza Akbarzadeh, Molood Mahdipour, Mahdi Nouri, Mohammad Adv Pharm Bull Research Article Purpose: Stem cells can exhibit restorative effects with the commitment to functional cells.Cell-imprinted topographies provide adaptable templates and certain dimensions for thedifferentiation and bioactivity of stem cells. Cell sheet technology using the thermo-responsivepolymers detaches the "cell sheets" easier with less destructive effects on the extracellularmatrix (ECM). Here, we aim to dictate keratinocyte-like differentiation of mesenchymal stemcells (MSCs) by using combined cell imprinting and sheet technology. Methods: We developed the poly dimethyl siloxane (PDMS) substrate having keratinocytecell-imprinted topography grafted with the PNIPAAm polymer. Adipose tissue-derived MSCs(AT-MSCs) were cultured on PDMS substrate for 14 days and keratinocyte-like differentiationmonitored via the expression of involucrin, P63, and cytokeratin 14. Results: Data showed the efficiency of the current protocol in the fabrication of PDMSmolds. The culture of AT-MSCs induced typical keratinocyte morphology and up-regulatedthe expression of cytokeratin-14, Involucrin, and P63 compared to AT-MSCs cultured on theplastic surface (P < 0.05). Besides, KLC sheets were generated once slight changes occur in theenvironment temperature. Conclusion: These data showed the hypothesis that keratinocyte cell imprinted substrate canorient AT-MSCs toward KLCs by providing a specific niche and topography. Tabriz University of Medical Sciences 2022-03 2021-05-02 /pmc/articles/PMC9106954/ /pubmed/35620328 http://dx.doi.org/10.34172/apb.2022.034 Text en ©2022 The Authors. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Research Article
Keyhanvar, Neda
Zarghami, Nosratollah
Seifalian, Alexander
Keyhanvar, Peyman
Sarvari, Rana
Salehi, Roya
Rahbarghazi, Reza
Ranjkesh, Mohammadreza
Akbarzadeh, Molood
Mahdipour, Mahdi
Nouri, Mohammad
The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title_full The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title_fullStr The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title_full_unstemmed The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title_short The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and "KLC Sheet" Formation
title_sort combined thermoresponsive cell-imprinted substrate, induced differentiation, and "klc sheet" formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106954/
https://www.ncbi.nlm.nih.gov/pubmed/35620328
http://dx.doi.org/10.34172/apb.2022.034
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