Sauer Heinrich, Ruhe Carola, Müller Jörg P, Schmelter Maike, D'Souza Rochelle, Wartenberg Maria
Department of Physiology, Justus Liebig University, Giessen, Germany.
Methods Mol Biol. 2008;477:397-418. doi: 10.1007/978-1-60327-517-0_30.
Deciphering the differentiation pathway of embryonic stem (ES) cells is a challenging task not only for basic research, but also for clinicians who intend to use ES cells for cell transplantation approaches. We have shown that reactive oxygen species (ROS) play a primordial role in the differentiation of mouse ES cells toward the cardiovascular cell lineage. During differentiation, ES cells robustly generate ROS, which interfere with signaling pathways that direct cardiac and vascular commitment. Differentiating ES cells expression of Nox-1, Nox-2, and Nox-4 has been demonstrated. We have shown that mechanical strain application to embyoid bodies grown from ES cells initiates the cardiovascular differentiation program. Under these conditions, a burst of ROS generation occurs which is followed by induction of Nox-1 and Nox-4 and a feed-forward upregulation of ROS production.
解析胚胎干细胞(ES细胞)的分化途径不仅对基础研究来说是一项具有挑战性的任务,对于那些打算将ES细胞用于细胞移植方法的临床医生而言也是如此。我们已经表明,活性氧(ROS)在小鼠ES细胞向心血管细胞谱系的分化过程中起着至关重要的作用。在分化过程中,ES细胞大量产生活性氧,这些活性氧会干扰指导心脏和血管定向分化的信号通路。已证实分化的ES细胞表达Nox-1、Nox-2和Nox-4。我们已经表明,对由ES细胞生长而来的拟胚体施加机械应变可启动心血管分化程序。在这些条件下,会出现一阵活性氧的产生,随后是Nox-1和Nox-4的诱导以及活性氧产生的前馈上调。