Department of Developmental Genetics, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, Japan.
Dev Neurobiol. 2011 Jun;71(6):458-73. doi: 10.1002/dneu.20859.
Neurons are morphologically characterized by long processes extending from a cell body. These processes, the dendrites and axon, are major sub-cellular compartments defined by morphological, molecular, and functional differences. However, evidence from vertebrates and invertebrates suggests that, based on molecular distribution, individual axons and dendrites are further divided into distinct compartments; many membrane molecules involved in axon guidance and synapse formation are localized to specific segments of axons or dendrites that share a boundary of localization. In this review, we describe recent progress in understanding the mechanisms of intra-neurite patterning, and discuss its potential roles in the development and function of the nervous system. Each protein employs different ways to achieve compartment-specific localization; some membrane molecules localize via cell-autonomous ability of neurons, while others require extrinsic signals for localization. The underlying regulatory mechanisms include transcriptional regulation, local translation, diffusion barrier, endocytosis, and selective membrane targeting. We propose that intra-neurite compartmentalization could provide platforms for structural and functional diversification of individual neurons.
神经元的形态学特征是由从细胞体延伸出的长突起(树突和轴突)决定的。这些突起是由形态、分子和功能差异定义的主要亚细胞区室。然而,来自脊椎动物和无脊椎动物的证据表明,根据分子分布,单个轴突和树突进一步分为不同的区室;许多参与轴突导向和突触形成的膜分子定位于共享定位边界的轴突或树突的特定段。在这篇综述中,我们描述了理解神经元内突模式形成机制的最新进展,并讨论了其在神经系统发育和功能中的潜在作用。每种蛋白质都采用不同的方法来实现特定区室的定位;一些膜分子通过神经元的自主能力定位,而另一些则需要外部信号进行定位。潜在的调节机制包括转录调节、局部翻译、扩散屏障、内吞作用和选择性膜靶向。我们提出,神经元内突区室化可以为单个神经元的结构和功能多样化提供平台。