Taschenberger Holger, Woehler Andrew, Neher Erwin
Department of Molecular Neurobiology, Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany; Center for Nanoscale Microscopy and Molecular Physiology of the Brain, 37073 Göttingen, Germany;
Center for Nanoscale Microscopy and Molecular Physiology of the Brain, 37073 Göttingen, Germany; Emeritus Group Membrane Biophysics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Proc Natl Acad Sci U S A. 2016 Aug 2;113(31):E4548-57. doi: 10.1073/pnas.1606383113. Epub 2016 Jul 18.
Glutamatergic synapses show large variations in strength and short-term plasticity (STP). We show here that synapses displaying an increased strength either after posttetanic potentiation (PTP) or through activation of the phospholipase-C-diacylglycerol pathway share characteristic properties with intrinsically strong synapses, such as (i) pronounced short-term depression (STD) during high-frequency stimulation; (ii) a conversion of that STD into a sequence of facilitation followed by STD after a few conditioning stimuli at low frequency; (iii) an equalizing effect of such conditioning stimulation, which reduces differences among synapses and abolishes potentiation; and (iv) a requirement of long periods of rest for reconstitution of the original STP pattern. These phenomena are quantitatively described by assuming that a small fraction of "superprimed" synaptic vesicles are in a state of elevated release probability (p ∼ 0.5). This fraction is variable in size among synapses (typically about 30%), but increases after application of phorbol ester or during PTP. The majority of vesicles, released during repetitive stimulation, have low release probability (p ∼ 0.1), are relatively uniform in number across synapses, and are rapidly recruited. In contrast, superprimed vesicles need several seconds to be regenerated. They mediate enhanced synaptic strength at the onset of burst-like activity, the impact of which is subject to modulation by slow modulatory transmitter systems.
谷氨酸能突触在强度和短期可塑性(STP)方面表现出很大差异。我们在此表明,在强直后增强(PTP)后或通过磷脂酶 - C - 二酰甘油途径激活而显示出增强强度的突触,与内在强突触具有共同的特征属性,例如:(i)在高频刺激期间明显的短期抑制(STD);(ii)在低频下经过几次条件刺激后,这种STD转变为一连串的易化,随后是STD;(iii)这种条件刺激的均衡作用,它减少了突触之间的差异并消除了增强作用;以及(iv)需要长时间的休息来重建原始的STP模式。通过假设一小部分“超预充”突触小泡处于释放概率升高的状态(p ∼ 0.5),可以对这些现象进行定量描述。这个比例在不同突触之间大小可变(通常约为30%),但在应用佛波酯后或PTP期间会增加。在重复刺激期间释放的大多数小泡具有低释放概率(p ∼ 0.1),在突触间数量相对均匀,并且能快速补充。相比之下,超预充小泡需要几秒钟才能再生。它们在爆发样活动开始时介导增强的突触强度,其影响受到缓慢调节性递质系统的调节。