Title of article :
The Combined Thermoresponsive Cell-Imprinted Substrate, Induced Differentiation, and KLC Sheet Formation
Author/Authors :
Keyhanvar ، Neda , Zarghami ، Nosratollah Department of Medical Biotechnology - Faculty of Advanced Medical Sciences - Tabriz University of Medical Sciences , Seifalian ، Alexander Nanotechnology and Regenerative Medicine Centre (Ltd) - London BioScience Innovation Centre , Keyhanvar ، Peyman Department of Medical Nanotechnology - Faculty of Advanced Medical Sciences - Tabriz University of Medical Sciences , Sarvari ، Rana Infectious and Tropical Diseases Research Center - Tabriz University of Medical Sciences , Salehi ، Roya Department of Medical Nanotechnology - Faculty of Advanced Medical Sciences - Tabriz University of Medical Sciences , Rahbarghazi ، Reza , Ranjkesh ، Mohammadreza Dermatology Dermopharmacy Research Team and Department of Dermatology - Sina Hospital - Tabriz University of Medical Sciences , Akbarzadeh ، Molood , Mahdipour ، Mahdi , Nouri ، Mohammad
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 (MSCs) 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 MSCs (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.
Keywords :
Adipose tissue , derived mesenchymal stem cells , Cell , imprinting , Cell sheet engineering , Differentiation , Poly N , Isopropyl acrylamide (PNIPAAm) , Topography
Journal title :
Advanced Pharmaceutical Bulletin
Journal title :
Advanced Pharmaceutical Bulletin