Smirnova Tatiana, Segall Jeffrey E
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461 , USA.
Cell Adh Migr. 2007 Oct-Dec;1(4):165-70. doi: 10.4161/cam.1.4.5305. Epub 2007 Oct 15.
Chemotaxis is the directed movement of a cell towards a gradient of chemicals such as chemokines or growth factors. This phenomenon can be studied in organisms ranging from bacteria to mammalian cells, and here we will focus on eukaryotic amoeboid chemotaxis. Chemotactic responses are mediated by two major classes of receptors: GPCR's and RTK's, with multiple pathways signaling downstream of them, certain ones functioning in parallel. In this review we address two important features of amoeboid chemotaxis that will be important for further advances in the field. First, the application of in vivo imaging will be critical for providing insight into the functional requirements for chemotactic responses. We will briefly cover a number of systems in which in vivo imaging is providing new insights. Second, due to the network-type design of signaling pathways of eukaryotic chemotaxis, more refined phenotypic analysis will be necessary, and we will discuss recent analyses of the role of the phosphoinositide 3-kinase pathway in this light. We will close with some speculations regarding future applications of more detailed in vivo analysis and mechanistic understanding of eukaryotic amoeboid chemotaxis.
趋化性是细胞朝着趋化因子或生长因子等化学物质梯度的定向运动。这种现象可以在从细菌到哺乳动物细胞等各种生物体中进行研究,在这里我们将重点关注真核变形虫趋化性。趋化反应由两大类受体介导:G蛋白偶联受体(GPCR)和受体酪氨酸激酶(RTK),它们下游有多个信号通路,其中一些并行发挥作用。在这篇综述中,我们阐述了变形虫趋化性的两个重要特征,这对于该领域的进一步发展至关重要。首先,体内成像的应用对于深入了解趋化反应的功能需求至关重要。我们将简要介绍一些体内成像正在提供新见解的系统。其次,由于真核趋化性信号通路的网络型设计,需要更精细的表型分析,我们将据此讨论磷脂酰肌醇3激酶途径作用的最新分析。我们将以一些关于更详细的体内分析的未来应用以及对真核变形虫趋化性的机制理解的推测作为结尾。