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

Author:

Keyhanvar Neda123ORCID,Zarghami Nosratollah2,Seifalian Alexander4,Keyhanvar Peyman5,Sarvari Rana6,Salehi Roya5,Rahbarghazi Reza17,Ranjkesh Mohammadreza8,Akbarzadeh Molood39,Mahdipour Mahdi110,Nouri Mohamamd123ORCID

Affiliation:

1. Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

2. Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

3. Stem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz Iran.

4. Nanotechnology and Regenerative Medicine Centre (Ltd), the London BioScience Innovation Centre, London, UK.

5. Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

6. Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

7. Department of Applied Cell Sciences, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

8. Dermatology & Dermopharmacy Research Team and Department of Dermatology, Sina Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.

9. Department of Cellular and Molecular Biology, Faculty of Biological Science, Azarbaijan Shahid Madani University, Tabriz, Iran.

10. Department of Reproductive Biology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

Abstract

Purpose: Stem cells can exhibit restorative effects with the commitment to functional cells. Cell-imprinted topographies provide adaptable templates and certain dimensions for the differentiation and bioactivity of stem cells. Cell sheet technology using the thermo-responsive polymers detaches the "cell sheets" easier with less destructive effects on the extracellular matrix (ECM). Here, we aim to dictate keratinocyte-like differentiation of mesenchymal stem cells by using combined cell imprinting and sheet technology. Methods: We developed the poly dimethyl siloxane (PDMS) substrate having keratinocyte cell-imprinted topography grafted with the PNIPAAm polymer. Adipose tissue-derived mesenchymal stem cells (AT-MSCs) were cultured on PDMS substrate for 14 days and keratinocyte-like differentiation monitored via the expression of involucrin, P63, and cytokeratin 14. Results: Data showed the efficiency of the current protocol in the fabrication of PDMS molds. The culture of AT-MSCs induced typical keratinocyte morphology and up-regulated the expression of cytokeratin-14, Involucrin, and P63 compared to AT-MSCs cultured on the plastic surface (p<0.05). Besides, KLC sheets were generated once slight changes occur in the environment temperature. Conclusion: These data showed the hypothesis that keratinocyte cell imprinted substrate can orient AT-MSCs toward KLCs by providing a specific niche and topography.

Publisher

Maad Rayan Publishing Company

Subject

General Pharmacology, Toxicology and Pharmaceutics,Pharmaceutical Science

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