Institute of Anatomy and Cell Biology, Department of Functional Neuroanatomy, Heidelberg University, Heidelberg, Germany.
Present address: Neuroscience Research Center, Charité Universitätsmedizin, Berlin, Germany.
J Physiol. 2018 Apr 15;596(8):1485-1499. doi: 10.1113/JP274885. Epub 2018 Jan 4.
Bassoon and Piccolo do not mediate basal synaptic vesicle release at a high-frequency synapse. Knockdown of Bassoon increases short-term depression at the calyx of Held. Both Bassoon and Piccolo have shared functions in synaptic vesicle replenishment during high-frequency synaptic transmission. Piccolo organizes the readily releasable pool of synaptic vesicles. It safeguards a fraction of them to be not immediately available for action potential-induced release. This enables the synapse to sustain high-frequency synaptic transmission over long periods.
Synaptic vesicles (SVs) are released at the active zone (AZ), a specialized region of the presynaptic plasma membrane organized by a highly interconnected network of multidomain proteins called the cytomatrix of the active zone (CAZ). Two core components of the CAZ are the large, highly homologous scaffolding proteins Bassoon and Piccolo, whose function is not well understood. To investigate their role in synaptic transmission, we established the small hairpin RNA (shRNA)-mediated in vivo knockdown (KD) of Bassoon and Piccolo at the rat calyx of Held synapse. KD of Bassoon and Piccolo, separately or simultaneously, did not affect basic SV release. However, short-term depression (STD) was prominently increased by the KD of Bassoon, whereas KD of Piccolo only had a minor effect. The observed alterations in STD were readily explained by reduced SV replenishment in synapses deficient in either of the proteins. Thus, the regulation of SV refilling during ongoing synaptic activity is a shared function of Bassoon and Piccolo, although Bassoon appears to be more efficient. Moreover, we observed the recruitment of slowly-releasing SVs of the readily-releasable pool (RRP), which are normally not available for action potential-induced release, during high-frequency stimulation in Piccolo-deficient calyces. Therefore, the results obtained in the present study suggest a novel and specific role for Piccolo in the organization of the subpools of the RRP.
巴松和短笛在高频突触中不介导基底突触小泡释放。巴松的敲低增加了海氏角回的短期抑郁。巴松和短笛在高频突触传递过程中具有共同的功能,以补充突触小泡。短笛组织了易于释放的突触小泡池。它保护其中的一部分不能立即用于动作电位诱导的释放。这使突触能够在长时间内维持高频突触传递。
突触小泡 (SVs) 在活性区 (AZ) 释放,AZ 是一个由高度相互连接的多域蛋白网络组成的特殊的突触前质膜区域,称为活性区细胞基质 (CAZ)。CAZ 的两个核心组件是大型、高度同源的支架蛋白巴松和短笛,其功能尚不清楚。为了研究它们在突触传递中的作用,我们在大鼠海氏角回突触中建立了小发夹 RNA (shRNA) 介导的体内巴松和短笛敲低 (KD)。巴松和短笛的 KD ,单独或同时,不影响基本 SV 释放。然而,巴松的 KD 显著增加了短期抑郁 (STD),而短笛的 KD 只有轻微的影响。观察到的 STD 改变很容易用在缺乏任一种蛋白的突触中 SV 再填充减少来解释。因此,在持续的突触活动中 SV 再填充的调节是巴松和短笛的共同功能,尽管巴松似乎更有效。此外,我们观察到在 Piccolo 缺陷的海氏角回中,在高频刺激期间,快速释放池 (RRP) 的缓慢释放 SV 被募集,这些 SV 通常不能用于动作电位诱导的释放。因此,本研究获得的结果表明,短笛在 RRP 的亚池的组织中具有新的和特定的作用。