Departments of Neurobiology, Otolaryngology, and Bioengineering, University of Pittsburgh School of Medicine, Biomedical Science Tower 3, Rm. 10016, 3501 Fifth Avenue, Pittsburgh, PA, 15261, USA.
Department of Physiology and Pharmacology, Wake Forest School of Medicine, PTCRC, Rm. 230, 115 South Chestnut Street, Winston-Salem, NC, 27157, USA.
Sci Rep. 2020 Oct 9;10(1):16899. doi: 10.1038/s41598-020-73050-y.
Before the onset of hearing, cochlea-generated patterns of spontaneous spike activity drive the maturation of central auditory circuits. In the glycinergic sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO) this spontaneous activity guides the strengthening and silencing of synapses which underlies tonotopic map refinement. However, the mechanisms by which patterned activity regulates synaptic refinement in the MNTB-LSO pathway are still poorly understood. To address this question, we recorded from LSO neurons in slices from prehearing mice while stimulating MNTB afferents with stimulation patterns that mimicked those present in vivo. We found that these semi-natural stimulation patterns reliably elicited a novel form of long-term potentiation (LTP) of MNTB-LSO synapses. Stimulation patterns that lacked the characteristic high-frequency (200 Hz) component of prehearing spike activity failed to elicit potentiation. LTP was calcium dependent, required the activation of both g-protein coupled GABA and metabotropic glutamate receptors and involved an increase in postsynaptic glycine receptor-mediated currents. Our results provide a possible mechanism linking spontaneous spike bursts to tonotopic map refinement and further highlight the importance of the co-release of GABA and glutamate from immature glycinergic MNTB terminals.
在听力出现之前,耳蜗产生的自发性尖峰活动模式驱动着中枢听觉回路的成熟。在来自梯形体中间核(MNTB)到外侧上橄榄核(LSO)的甘氨酸能声音定位途径中,这种自发性活动指导着突触的强化和沉默,这是音位图谱细化的基础。然而,模式活动调节 MNTB-LSO 途径中突触细化的机制仍知之甚少。为了解决这个问题,我们在听力前的小鼠切片中记录 LSO 神经元的活动,同时用模拟体内存在的刺激模式刺激 MNTB 传入纤维。我们发现,这些半自然刺激模式可靠地引发了 MNTB-LSO 突触的一种新形式的长时程增强(LTP)。缺乏听力前尖峰活动特征性高频(200Hz)成分的刺激模式未能引发增强。LTP 依赖于钙,需要激活 G 蛋白偶联 GABA 和代谢型谷氨酸受体,并涉及突触后甘氨酸受体介导电流的增加。我们的结果提供了一种可能的机制,将自发性尖峰爆发与音位图谱细化联系起来,并进一步强调了不成熟甘氨酸能 MNTB 末梢 GABA 和谷氨酸共同释放的重要性。