Valcourt Ulrich, Carthy Jonathon, Okita Yukari, Alcaraz Lindsay, Kato Mitsuyasu, Thuault Sylvie, Bartholin Laurent, Moustakas Aristidis
Inserm U1052, Centre de Recherche en Cancérologie de Lyon, 69000, Lyon, France.
CNRS UMR 5286, Centre de Recherche en Cancérologie de Lyon, 69000, Lyon, France.
Methods Mol Biol. 2016;1344:147-81. doi: 10.1007/978-1-4939-2966-5_9.
In recent years, the importance of the cell biological process of epithelial-mesenchymal transition (EMT) has been established via an exponentially growing number of reports. EMT has been documented during embryonic development, tissue fibrosis, and cancer progression in vitro, in animal models in vivo and in human specimens. EMT relates to many molecular and cellular alterations that occur when epithelial cells undergo a switch in differentiation that generates mesenchymal-like cells with newly acquired migratory and invasive properties. In addition, EMT relates to a nuclear reprogramming similar to the one occurring in the generation of induced pluripotent stem cells. Via such a process, EMT is gradually established to promote the generation and maintenance of adult tissue stem cells which under disease states such as cancer, are known as cancer stem cells. EMT is induced by developmental growth factors, oncogenes, radiation, and hypoxia. A prominent growth factor that causes EMT is transforming growth factor β (TGF-β).A series of molecular and cellular techniques can be applied to define and characterize the state of EMT in diverse biological samples. These methods range from DNA and RNA-based techniques that measure the expression of key EMT regulators and markers of epithelial or mesenchymal differentiation to functional assays of cell mobility, invasiveness and in vitro stemness. This chapter focuses on EMT induced by TGF-β and provides authoritative protocols and relevant reagents and citations of key publications aiming at assisting newcomers that enter this prolific area of biomedical sciences, and offering a useful reference tool to pioneers and aficionados of the field.
近年来,通过数量呈指数级增长的报告,上皮-间质转化(EMT)这一细胞生物学过程的重要性已得到确立。在胚胎发育、组织纤维化以及体外、动物模型体内和人类标本中的癌症进展过程中,均已记录到EMT现象。EMT涉及上皮细胞在分化转变时发生的许多分子和细胞改变,这种转变会产生具有新获得的迁移和侵袭特性的间充质样细胞。此外,EMT还涉及一种类似于诱导多能干细胞产生过程中发生的核重编程。通过这样一个过程,EMT逐渐被证实可促进成体组织干细胞的产生和维持,在诸如癌症等疾病状态下,这些干细胞被称为癌症干细胞。EMT由发育生长因子、癌基因、辐射和缺氧诱导。导致EMT的一种重要生长因子是转化生长因子β(TGF-β)。一系列分子和细胞技术可用于定义和表征不同生物样品中的EMT状态。这些方法包括基于DNA和RNA的技术,用于测量关键EMT调节因子的表达以及上皮或间充质分化的标志物,还包括细胞迁移、侵袭和体外干性的功能测定。本章重点介绍由TGF-β诱导的EMT,并提供权威方案以及相关试剂和关键出版物的引用,旨在帮助初涉这一生物医学科学丰富领域的新手,并为该领域的先驱者和爱好者提供有用的参考工具。