Brevini Tiziana A L, Manzoni Elena F M, Arcuri Sharon, Gandolfi Fulvio
Department of Health, Animal Science and Food Safety, Università degli Studi di Milano, Milano 20122, Italy.
Anim Reprod. 2020 May 22;16(1):18-23. doi: 10.21451/1984-3143-AR2018-0096.
Cell fate specification, gene expression and spatial restriction are process finely tuned by epigenetic regulatory mechanisms. At the same time, mechanical forces have been shown to be crucial to drive cell plasticity and boost differentiation. Indeed, several studies have demonstrated that transitions along different specification states are strongly influenced by 3D rearrangement and mechanical properties of the surrounding microenvironment, that can modulate both cell potency and differentiation, through the activation of specific mechanosensing-related pathways. An overview of small molecule ability to modulate cell plasticity and define cell fate is here presented and results, showing the possibility to erase the epigenetic signature of adult dermal fibroblasts and convert them into insulin-producing cells (EpiCC) are described. The beneficial effects exerted on such processes, when cells are homed on an adequate substrate, that shows " tissue-like stiffness are also discussed and the contribution of the Hippo signalling mechano-transduction pathway as one of the mechanisms involved is examined. In addition, results obtained using a genetically modified fibroblast cell line, expressing the enhanced green fluorescent protein (eGFP) under the control of the porcine insulin gene (INS) promoter (INS-eGFP transgenic pigs), are reported. This model offers the advantage to monitor the progression of cell conversion in real time mode. All these observations have a main role in order to allow a swift scale-up culture procedure, essential for cell therapy and tissue engineering applied to human regenerative medicine, and fundamental to ensure an efficient translation process from the results obtained at the laboratory bench to the patient bedside. Moreover, the creation of reliable in vitro model represents a key point to ensure the development of more physiological models that, in turn, may reduce the number of animals used, implementing non-invasive investigations and animal welfare and protection.
细胞命运特化、基因表达和空间限制是由表观遗传调控机制精细调节的过程。与此同时,机械力已被证明对驱动细胞可塑性和促进分化至关重要。事实上,多项研究表明,沿着不同特化状态的转变受到周围微环境的三维重排和机械特性的强烈影响,这可以通过激活特定的机械传感相关途径来调节细胞潜能和分化。本文概述了小分子调节细胞可塑性和定义细胞命运的能力,并描述了相关结果,这些结果表明有可能消除成年真皮成纤维细胞的表观遗传特征并将其转化为胰岛素产生细胞(EpiCC)。还讨论了细胞接种在具有“组织样硬度”的合适底物上时对这些过程产生的有益影响,并研究了河马信号机械转导途径作为其中一种涉及机制的贡献。此外,还报告了使用在猪胰岛素基因(INS)启动子控制下表达增强型绿色荧光蛋白(eGFP)的基因修饰成纤维细胞系(INS-eGFP转基因猪)获得的结果。该模型具有实时监测细胞转化进程的优势。所有这些观察结果对于实现快速放大培养程序至关重要,这对于应用于人类再生医学的细胞治疗和组织工程必不可少,也是确保从实验室工作台获得的结果有效转化到患者床边的基础。此外,创建可靠的体外模型是确保开发更具生理性模型的关键,这反过来可能会减少所用动物的数量,实施非侵入性研究并提高动物福利和保护水平。