Mazel Tomáš
Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00, Prague 2, Czech Republic.
State Institute for Drug Control, Šrobárova 48, 100 41, Prague 10, Czech Republic.
Protoplasma. 2017 May;254(3):1241-1258. doi: 10.1007/s00709-017-1075-2. Epub 2017 Mar 14.
Cell polarity, the asymmetric organization of cellular components along one or multiple axes, is present in most cells. From budding yeast cell polarization induced by pheromone signaling, oocyte polarization at fertilization to polarized epithelia and neuronal cells in multicellular organisms, similar mechanisms are used to determine cell polarity. Crucial role in this process is played by signaling lipid molecules, small Rho family GTPases and Par proteins. All these signaling circuits finally govern the cytoskeleton, which is responsible for oriented cell migration, cell shape changes, and polarized membrane and organelle trafficking. Thus, typically in the process of cell polarization, most cellular constituents become polarized, including plasma membrane lipid composition, ion concentrations, membrane receptors, and proteins in general, mRNA, vesicle trafficking, or intracellular organelles. This review gives a brief overview how these systems talk to each other both during initial symmetry breaking and within the signaling feedback loop mechanisms used to preserve the polarized state.
细胞极性,即细胞成分沿一个或多个轴的不对称组织,存在于大多数细胞中。从信息素信号诱导的芽殖酵母细胞极化、受精时的卵母细胞极化到多细胞生物中的极化上皮细胞和神经元细胞,都使用类似的机制来确定细胞极性。信号脂质分子、小Rho家族GTP酶和Par蛋白在这一过程中发挥着关键作用。所有这些信号通路最终控制着细胞骨架,细胞骨架负责定向细胞迁移、细胞形状变化以及极化的膜和细胞器运输。因此,在细胞极化过程中,通常大多数细胞成分都会发生极化,包括质膜脂质组成、离子浓度、膜受体以及一般的蛋白质、mRNA、囊泡运输或细胞内细胞器。本综述简要概述了这些系统在初始对称性破坏期间以及用于维持极化状态的信号反馈回路机制中是如何相互作用的。