Laboratories for Physical Biology, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan.
J Cell Sci. 2012 Nov 1;125(Pt 21):5138-50. doi: 10.1242/jcs.108373. Epub 2012 Aug 16.
A key signaling event that is responsible for gradient sensing in eukaryotic cell chemotaxis is a phosphatidylinositol (PtdIns) lipid reaction system. The self-organization activity of this PtdIns lipid system induces an inherent polarity, even in the absence of an external chemoattractant gradient, by producing a localized PtdIns (3,4,5)-trisphosphate [PtdIns(3,4,5)P(3)]-enriched domain on the membrane. Experimentally, we found that such a domain could exhibit two types of behavior: (1) it could be persistent and travel on the membrane, or (2) be stochastic and transient. Taking advantage of the simultaneous visualization of PtdIns(3,4,5)P(3) and the enzyme phosphatase and tensin homolog (PTEN), for which PtdIns(3,4,5)P(3) is a substrate, we statistically demonstrated the inter-dependence of their spatiotemporal dynamics. On the basis of this statistical analysis, we developed a theoretical model for the self-organization of PtdIns lipid signaling that can accurately reproduce both persistent and transient domain formation; these types of formations can be explained by the oscillatory and excitability properties of the system, respectively.
在真核细胞化学趋性中负责梯度感应的一个关键信号事件是磷脂酰肌醇(PtdIns)脂质反应系统。该 PtdIns 脂质系统的自组织活性通过在膜上产生局部富含 PtdIns(3,4,5)-三磷酸 [PtdIns(3,4,5)P(3)] 的域,即使在没有外部趋化梯度的情况下,也会诱导固有极性。在实验中,我们发现这样的域可以表现出两种行为:(1)它可以持续存在并在膜上移动,或者(2)是随机和瞬态的。利用 PtdIns(3,4,5)P(3)和磷酸酶和张力蛋白同源物(PTEN)的同时可视化,PTEN 是 PtdIns(3,4,5)P(3)的底物,我们从统计学上证明了它们时空动力学的相互依赖性。基于该统计分析,我们开发了一个用于 PtdIns 脂质信号自组织的理论模型,该模型可以准确再现持续和瞬态域的形成;这两种形成类型可以分别通过系统的振荡和兴奋性特性来解释。