Van der Kloot W, Naves L A
Department of Physiology and Biophysics, Health Sciences Center, State University at Stony Brook, New York 11794-8661, USA.
Biophys J. 1996 May;70(5):2175-84. doi: 10.1016/S0006-3495(96)79783-7.
The current model does not account adequately for the characteristics of miniature endplate currents (MEPCs). We do not understand their relatively slow rise, the shape of their rise, their variable and sometimes prolonged decay, and the correlation between amplitude and decay time. If we assume that ACh is released from the vesicle through a pore and that the vesicle enlarges as it takes on additional transmitter, the predictions are more like MEPCs. However, previous measurements showed that after quantal size was increased the vesicles in the terminal were not enlarged. This need not be a problem, because some of the ACh is added to vesicles positioned at the active zones, a process known as second-stage loading. By using the false transmitter precursor monoethylcholine we provide additional evidence for second-stage loading. The distribution of quantal sizes at the junction usually does not follow a normal probability distribution; it is skewed to the right. The skew can be accounted for by a model incorporating second-stage loading in which the vesicles are released randomly, without regard to their ACh content. If the vesicles increase in size when they contain more transmitter, only vesicles at the active zone need swell.
当前模型并未充分考虑微型终板电流(MEPCs)的特性。我们不理解它们相对缓慢的上升过程、上升的形状、其可变且有时延长的衰减过程,以及幅度与衰减时间之间的相关性。如果我们假设乙酰胆碱(ACh)通过一个孔从囊泡中释放出来,并且囊泡在摄取额外递质时会增大,那么预测结果会更类似于MEPCs。然而,先前的测量表明,在量子大小增加后,终末中的囊泡并未增大。这不一定是个问题,因为一些乙酰胆碱会被添加到位于活动区的囊泡中,这一过程称为第二阶段装载。通过使用假递质前体单乙基胆碱,我们为第二阶段装载提供了额外证据。接头处量子大小的分布通常不遵循正态概率分布;它向右偏斜。这种偏斜可以通过一个包含第二阶段装载的模型来解释,在该模型中,囊泡随机释放,而不考虑其乙酰胆碱含量。如果囊泡在含有更多递质时会增大,那么只有活动区的囊泡需要膨胀。