Feng Zhong-Ping, Grigoriev Nikita, Munno David, Lukowiak Ken, MacVicar Brian A, Goldberg Jeffrey I, Syed Naweed I
Respiratory and Neuroscience Research Groups, Faculty of Medicine, University of Calgary, 3330-Hospital Drive, NW, Calgary, Alberta, Canada T2N 4N1.
J Physiol. 2002 Feb 15;539(Pt 1):53-65. doi: 10.1113/jphysiol.2001.013125.
Calcium (Ca2+) channel clustering at specific presynaptic sites is a hallmark of mature synapses. However, the spatial distribution patterns of Ca2+ channels at newly formed synapses have not yet been demonstrated. Similarly, it is unclear whether Ca2+ 'hotspots' often observed at the presynaptic sites are indeed target cell contact specific and represent a specialized mechanism by which Ca2+ channels are targeted to select synaptic sites. Utilizing both soma-soma paired (synapsed) and single neurons from the mollusk Lymnaea, we have tested the hypothesis that differential gradients of voltage-dependent Ca2+ signals develop in presynaptic neuron at its contact point with the postsynaptic neuron; and that these Ca2+ hotspots are target cell contact specific. Fura-2 imaging, or two-photon laser scanning microscopy of Calcium Green, was coupled with electrophysiological techniques to demonstrate that voltage-induced Ca2+ gradients (hotspots) develop in the presynaptic cell at its contact point with the postsynaptic neuron, but not in unpaired single cells. The incidence of Ca2+ hotspots coincided with the appearance of synaptic transmission between the paired cells, and these gradients were target cell contact specific. In contrast, the voltage-induced Ca2+ signal in unpaired neurons was uniformly distributed throughout the somata; a similar pattern of Ca2+ gradient was observed in the presynaptic neuron when it was soma-soma paired with a non-synaptic partner cell. Moreover, voltage clamp recording techniques, in conjunction with a fast, optical differential perfusion system, were used to demonstrate that the total whole-cell Ca2+ (or Ba2+) current density in single and paired cells was not significantly different. However, the amplitude of Ba2+ current was significantly higher in the presynaptic cell at its contact side with the postsynaptic neurons, compared with non-contacted regions. In summary, this study demonstrates that voltage-induced Ca2+ hotspots develop in the presynaptic cell, concomitant with the appearance of synaptic transmission between the soma-soma paired cells. The appearance of Ca2+ gradients in presynaptic neurons is target cell contact specific and is probably due to a spatial redistribution of existing channels during synaptogenesis.
钙(Ca2+)通道在特定突触前位点的聚集是成熟突触的一个标志。然而,新生突触处Ca2+通道的空间分布模式尚未得到证实。同样,目前尚不清楚在突触前位点经常观察到的Ca2+“热点”是否确实具有靶细胞接触特异性,以及是否代表一种将Ca2+通道靶向特定突触位点的特殊机制。利用来自淡水螺的体细胞-体细胞配对(突触连接)和单个神经元,我们检验了以下假设:在突触前神经元与突触后神经元的接触点处,电压依赖性Ca2+信号会形成差异梯度;并且这些Ca2+热点具有靶细胞接触特异性。采用Fura-2成像或钙黄绿素的双光子激光扫描显微镜,并结合电生理技术,以证明电压诱导的Ca2+梯度(热点)在突触前细胞与突触后神经元的接触点处形成,但在未配对的单个细胞中不会形成。Ca2+热点的出现与配对细胞之间突触传递的出现相吻合,并且这些梯度具有靶细胞接触特异性。相比之下,未配对神经元中电压诱导的Ca2+信号在整个体细胞中均匀分布;当突触前神经元与非突触伙伴细胞进行体细胞-体细胞配对时,在突触前神经元中观察到类似的Ca2+梯度模式。此外,电压钳记录技术与快速光学微分灌注系统相结合,以证明单个细胞和配对细胞中的全细胞总Ca2+(或Ba2+)电流密度没有显著差异。然而,与非接触区域相比,突触前细胞与突触后神经元接触侧的Ba2+电流幅度明显更高。总之,这项研究表明,电压诱导的Ca2+热点在突触前细胞中形成,与体细胞-体细胞配对细胞之间突触传递的出现同时发生。突触前神经元中Ca2+梯度的出现具有靶细胞接触特异性,可能是由于突触形成过程中现有通道的空间重新分布所致。