Boiani Michele, Schöler Hans R
Max-Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, Mendelstrasse 7/Von-Esmarch Strasse 56, 48149 Münster, Germany.
Nat Rev Mol Cell Biol. 2005 Nov;6(11):872-84. doi: 10.1038/nrm1744.
Mammalian development requires the specification of over 200 cell types from a single totipotent cell. Investigation of the regulatory networks that are responsible for pluripotency in embryo-derived stem cells is fundamental to understanding mammalian development and realizing therapeutic potential. Extracellular signals and second messengers modulate cell-autonomous regulators such as OCT4, SOX2 and Nanog in a combinatorial complexity. Knowledge of this circuitry might reveal how to achieve phenotypic changes without the genetic manipulation of Oct4, Nanog and other toti/pluripotency-associated genes.
哺乳动物的发育需要从单个全能细胞分化出200多种细胞类型。研究胚胎干细胞中负责多能性的调控网络是理解哺乳动物发育和实现治疗潜力的基础。细胞外信号和第二信使以组合复杂性调节细胞自主调节因子,如OCT4、SOX2和Nanog。了解这一信号通路可能揭示如何在不进行Oct4、Nanog和其他与全能/多能性相关基因的基因操作的情况下实现表型变化。