Niell Cristopher M, Smith Stephen J
Neurosciences Program and Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA.
Annu Rev Physiol. 2004;66:771-98. doi: 10.1146/annurev.physiol.66.082602.095217.
Although development of the nervous system is inherently a process of dynamic change, until recently it has generally been investigated by inference from static images. However, advances in live optical imaging are now allowing direct observation of growth, synapse formation, and even incipient function in the developing nervous system, at length scales from molecules to cortical regions, and over timescales from milliseconds to months. In this review, we provide technical background and present examples of how these new methods, including confocal and two-photon microscopy, GFP-based markers, and functional indicators, are being applied to provide fresh insight into long-standing questions of neural development.
尽管神经系统的发育本质上是一个动态变化的过程,但直到最近,人们通常还是通过对静态图像的推断来进行研究。然而,实时光学成像技术的进步现在使我们能够直接观察发育中的神经系统中的生长、突触形成,甚至初期功能,观察范围从分子到皮质区域的长度尺度,以及从毫秒到数月的时间尺度。在这篇综述中,我们提供了技术背景,并举例说明这些新方法,包括共聚焦显微镜和双光子显微镜、基于绿色荧光蛋白的标记物以及功能指示剂,是如何被应用于为神经发育的长期问题提供新的见解。