Hall Benjamin J, Delaney Kerry R
Simon Fraser University, Burnaby, BC, Canada V5A 1S6.
J Physiol. 2002 Sep 15;543(Pt 3):819-34. doi: 10.1113/jphysiol.2002.024638.
We studied granule cells (GCs) in the intact frog olfactory bulb (OB) by combining whole-cell recordings and functional two-photon Ca(2+) imaging in an in vitro nose-brain preparation. GCs are local interneurones that shape OB output via distributed dendrodendritic inhibition of OB projection neurones, the mitral-tufted cells (MTCs). In contrast to MTCs, GCs exhibited a Ca(2+)-activated non-specific cation conductance (I(CAN)) that could be evoked through strong synaptic stimulation or suprathreshold current injection. Photolysis of the caged Ca(2+) chelator o-nitrophenol-EGTA resulted in activation of an inward current with a reversal potential within the range -20 to +10 mV. I(CAN) in GCs was suppressed by the intracellular Ca(2+) chelator BAPTA (0.5-5.0 mM), but not by EGTA (up to 5 mM). The current persisted in whole-cell recordings for up to 1.5 h post-breakthrough, was observed during perforated-patch recordings and was independent of ionotropic glutamate and GABA(A) receptor activity. In current-clamp mode, GC responses to synaptic stimulation consisted of an initial AMPA-mediated conductance followed by a late-phase APV-sensitive plateau (100-500 ms). BAPTA-mediated suppression of I(CAN) resulted in a selective reduction of the late component of the evoked synaptic potential, consistent with a positive feedback relationship between NMDA receptor (NMDAR) current and I(CAN). I(CAN) requires Ca(2+) influx either through voltage-gated Ca(2+) channels or possibly NMDARs, both of which have a high threshold for activation in GCs, predicting a functional role for this current in the selective enhancement of strong synaptic inputs to GCs.
我们通过在体外鼻脑制备物中结合全细胞记录和功能性双光子Ca(2+)成像,研究了完整青蛙嗅球(OB)中的颗粒细胞(GCs)。GCs是局部中间神经元,通过对OB投射神经元即二尖瓣-簇状细胞(MTCs)的分布式树突-树突抑制来塑造OB输出。与MTCs不同,GCs表现出一种Ca(2+)激活的非特异性阳离子电导(I(CAN)),可通过强突触刺激或阈上电流注入诱发。笼装Ca(2+)螯合剂邻硝基苯酚-乙二醇双乙酸(o-nitrophenol-EGTA)的光解导致内向电流的激活,其反转电位在-20至+10 mV范围内。GCs中的I(CAN)被细胞内Ca(2+)螯合剂BAPTA(0.5 - 5.0 mM)抑制,但不被EGTA(高达5 mM)抑制。该电流在全细胞记录中突破后可持续长达1.5小时,在穿孔膜片记录中也可观察到,且与离子型谷氨酸和GABA(A)受体活性无关。在电流钳模式下,GCs对突触刺激的反应包括初始的AMPA介导的电导,随后是晚期的APV敏感平台期(100 - 500毫秒)。BAPTA介导的I(CAN)抑制导致诱发突触电位晚期成分的选择性降低,这与NMDA受体(NMDAR)电流和I(CAN)之间的正反馈关系一致。I(CAN)需要通过电压门控Ca(2+)通道或可能通过NMDARs的Ca(2+)内流,这两者在GCs中都有较高的激活阈值,预示着该电流在选择性增强GCs的强突触输入方面具有功能作用。