CNRS, Laboratoire de Biologie du Développement, Paris, France.
Cell Adh Migr. 2010 Jul-Sep;4(3):458-82. doi: 10.4161/cam.4.3.12501. Epub 2010 Jul 27.
Although epithelial to mesenchymal transitions (EMT) are often viewed as a unique event, they are characterized by a great diversity of cellular processes resulting in strikingly different outcomes. They may be complete or partial, massive or progressive, and lead to the complete disruption of the epithelium or leave it intact. Although the molecular and cellular mechanisms of EMT are being elucidated owing chiefly from studies on transformed epithelial cell lines cultured in vitro or from cancer cells, the basis of the diversity of EMT processes remains poorly understood. Clues can be collected from EMT occuring during embryonic development and which affect equally tissues of ectodermal, endodermal or mesodermal origins. Here, based on our current knowledge of the diversity of processes underlying EMT of neural crest cells in the vertebrate embryo, we propose that the time course and extent of EMT do not depend merely on the identity of the EMT transcriptional regulators and their cellular effectors but rather on the combination of molecular players recruited and on the possible coordination of EMT with other cellular processes.
尽管上皮-间充质转化 (EMT) 通常被视为一个独特的事件,但它具有多种细胞过程的特点,导致截然不同的结果。它们可以是完全的或部分的,大量的或渐进的,并导致上皮的完全破坏或使其保持完整。尽管 EMT 的分子和细胞机制主要通过体外培养的转化上皮细胞系或癌细胞的研究来阐明,但 EMT 过程多样性的基础仍知之甚少。可以从胚胎发育过程中发生的 EMT 中收集线索,这些 EMT 同样影响外胚层、内胚层或中胚层来源的组织。在这里,基于我们目前对脊椎动物胚胎神经嵴细胞 EMT 所涉及的过程多样性的了解,我们提出 EMT 的时间进程和程度不仅取决于 EMT 转录调节因子及其细胞效应物的身份,还取决于募集的分子参与者的组合,以及 EMT 与其他细胞过程的可能协调。