Pan Feng, Gan Wen-Biao
Skirball Institute, Department of Physiology and Neuroscience, New York University School of Medicine, New York, New York 10016, USA.
Dev Neurobiol. 2008 May;68(6):771-8. doi: 10.1002/dneu.20630.
Dendritic spines are the postsynaptic sites of most excitatory synapses in the mammalian brain. With the advent of two-photon microscopy and transgenic mice expressing fluorescent proteins, dendritic spines can now be imaged in the living cerebral cortex over time scales ranging from seconds to years. Recent studies with this in vivo imaging approach have begun to provide important insights into the development and plasticity of dendritic spines in the intact brain. Here, we review these studies and discuss technical requirements for image acquisition. We envision that intravital two-photon imaging at the level of individual synapses will greatly expand our current understandings of how neuronal networks are assembled and modified throughout life.
树突棘是哺乳动物大脑中大多数兴奋性突触的突触后位点。随着双光子显微镜和表达荧光蛋白的转基因小鼠的出现,现在可以在活体大脑皮层中对树突棘进行成像,时间跨度从几秒到几年。最近采用这种体内成像方法的研究已经开始为完整大脑中树突棘的发育和可塑性提供重要见解。在这里,我们回顾这些研究并讨论图像采集的技术要求。我们设想,在单个突触水平上的活体双光子成像将极大地扩展我们目前对神经网络在整个生命过程中如何组装和修饰的理解。