Keyhanvar Neda, Zarghami Nosratollah, Seifalian Alexander, Keyhanvar Peyman, Sarvari Rana, Salehi Roya, Rahbarghazi Reza, Ranjkesh Mohammadreza, Akbarzadeh Molood, Mahdipour Mahdi, Nouri Mohammad
Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2022 Mar;12(2):356-365. doi: 10.34172/apb.2022.034. Epub 2021 May 2.
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. 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. 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 ( < 0.05). Besides, KLC sheets were generated once slight changes occur in theenvironment temperature. These data showed the hypothesis that keratinocyte cell imprinted substrate canorient AT-MSCs toward KLCs by providing a specific niche and topography.
干细胞可通过向功能细胞分化展现修复作用。细胞印记拓扑结构为干细胞的分化和生物活性提供了适应性模板和特定维度。利用热响应聚合物的细胞片技术能更轻松地分离“细胞片”,且对细胞外基质(ECM)的破坏作用更小。在此,我们旨在通过联合使用细胞印记和片技术来调控间充质干细胞(MSCs)向角质形成细胞样细胞分化。我们开发了接枝有聚N-异丙基丙烯酰胺(PNIPAAm)聚合物且具有角质形成细胞印记拓扑结构的聚二甲基硅氧烷(PDMS)底物。将脂肪组织来源的间充质干细胞(AT-MSCs)在PDMS底物上培养14天,并通过内披蛋白、P63和细胞角蛋白14的表达来监测角质形成细胞样细胞的分化。数据显示了当前方案在制造PDMS模具方面的效率。与在塑料表面培养的AT-MSCs相比,培养的AT-MSCs诱导出典型的角质形成细胞形态,并上调了细胞角蛋白-14、内披蛋白和P63的表达(P<0.05)。此外,一旦环境温度发生轻微变化,就会生成角质形成细胞样细胞片。这些数据表明了这样一个假设,即角质形成细胞印记底物可通过提供特定的微环境和拓扑结构使AT-MSCs向角质形成细胞样细胞定向分化。