Propst J W, Ko C P
Department of Biological Sciences, University of Southern California, Los Angeles 90089-0371.
J Neurosci. 1987 Nov;7(11):3654-64. doi: 10.1523/JNEUROSCI.07-11-03654.1987.
The active zone is a unique presynaptic membrane specialization that is believed to be the site of neurotransmitter release. To examine directly the relationship between active zone ultrastructure and synaptic efficacy, frog neuromuscular junctions were studied with a new technique combining electrophysiology, light microscopy, and freeze-fracture of identified single muscle fibers. This technique allows correlations to be made between quantal content (measured in low Ca2+ and high Mg2+ Ringer solution), endplate size, and active zone structure at the same neuromuscular junctions. By measuring physiological and morphological variables at the same junctions, the validity of structure-function correlations is significantly improved. Synaptic quantal content in 91 physiologically identified muscle fibers varied considerably and was only poorly correlated with endplate size, as shown in previous studies. To measure the total length of endplate branches, either a modified cholinesterase stain or rhodamine-labeled peanut agglutinin stain was used. When the same identified muscle fibers were freeze-fractured, active zones were exposed in 17 junctions. In a replica that contained a large part of one nerve terminal, there was no detectable gradient in active zone structure along the length of 3 different nerve terminal branches identifiable with both light and electron microscopy. The results from these 17 identified junctions indicate that quantal content per unit terminal length is positively correlated with the amount of active zone per unit terminal length. The estimated total active zone length and total number of active zone particles per junction are also positively correlated with the quantal content in these identified junctions. This study suggests that active zone size and spacing are better indicators of transmitter release than is endplate size and that the active zone may play an important role in regulating synaptic efficacy at the neuromuscular junction.
活性区是一种独特的突触前膜特化结构,被认为是神经递质释放的部位。为了直接研究活性区超微结构与突触效能之间的关系,采用一种结合电生理学、光学显微镜和对单个已识别肌肉纤维进行冷冻断裂的新技术,对青蛙神经肌肉接头进行了研究。该技术能够在同一神经肌肉接头上,将量子含量(在低钙和高镁林格氏液中测量)、终板大小和活性区结构联系起来。通过在同一接头上测量生理和形态学变量,显著提高了结构-功能相关性的有效性。如先前研究所示,91根经生理鉴定的肌肉纤维中的突触量子含量差异很大,且与终板大小的相关性很差。为了测量终板分支的总长度,使用了改良的胆碱酯酶染色或罗丹明标记的花生凝集素染色。当对相同的已识别肌肉纤维进行冷冻断裂时,在17个接头中暴露了活性区。在一个包含大部分单个神经末梢的复制品中,在通过光学显微镜和电子显微镜均可识别的3个不同神经末梢分支的长度上,未检测到活性区结构的梯度变化。来自这17个已识别接头的结果表明,单位末梢长度的量子含量与单位末梢长度的活性区数量呈正相关。每个接头的活性区总长度估计值和活性区颗粒总数也与这些已识别接头中的量子含量呈正相关。这项研究表明,活性区的大小和间距比终板大小更能反映递质释放情况,并且活性区可能在调节神经肌肉接头的突触效能中发挥重要作用。