Sethuramanujam Santhosh, Slaughter Malcolm M
Center for Neuroscience and Department of Physiology and Biophysics, University at Buffalo, Buffalo, New York
Center for Neuroscience and Department of Physiology and Biophysics, University at Buffalo, Buffalo, New York.
J Neurophysiol. 2014 Jul 1;112(1):193-203. doi: 10.1152/jn.00817.2013. Epub 2014 Apr 9.
Glutamate release at bipolar to ganglion cell synapses activates NMDA and AMPA/kainic acid (KA) ionotropic glutamate receptors. Their relative strength determines the output signals of the retina. We found that this balance is tightly regulated by presynaptic inhibition that preferentially suppresses NMDA receptor (NMDAR) activation. In transient ON-OFF neurons, block of GABA and glycine feedback enhanced total NMDAR charge by 35-fold in the ON response and 9-fold in the OFF compared with a 1.7-fold enhancement of AMPA/KA receptors. Blocking only glycine receptors enhanced the NMDAR excitatory postsynaptic current 10-fold in the ON and 2-fold in the OFF pathway. Blocking GABA(A) or GABA(C) receptors (GABA(C)Rs or GABA(A)Rs) produced small changes in total NMDAR charge. When both GABA(A)Rs and GABA(C)Rs were blocked, the total NMDAR charge increased ninefold in the ON and fivefold in the OFF pathway. This exposed a strong GABA(C)R feedback to bipolar cells that was suppressed by serial amacrine cell synapses mediated by GABA(A)Rs. The results indicate that NMDAR currents are large but latent, held in check by dual GABA and glycine presynaptic inhibition. One example of this controlled NMDAR activation is the cross talk between ON and OFF pathways. Blocking the ON pathway increased NMDAR relative strength in the OFF pathway. Stimulus prolongation similarly increased the NMDAR relative strength in the OFF response. This NMDAR enhancement was produced by a diminution in GABA and glycine feedback. Thus the retinal network recruits NMDAR pathways through presynaptic disinhibition.
双极细胞与神经节细胞突触处谷氨酸的释放会激活N-甲基-D-天冬氨酸(NMDA)以及α-氨基-3-羟基-5-甲基-4-异恶唑丙酸/海人酸(AMPA/KA)离子型谷氨酸受体。它们之间的相对强度决定了视网膜的输出信号。我们发现,这种平衡受到突触前抑制的严格调控,突触前抑制会优先抑制NMDA受体(NMDAR)的激活。在瞬态开-关神经元中,与AMPA/KA受体增强1.7倍相比,阻断GABA和甘氨酸反馈使开反应中总的NMDAR电荷增强了35倍,关反应中增强了9倍。仅阻断甘氨酸受体可使开通路中NMDAR兴奋性突触后电流增强10倍,关通路中增强2倍。阻断GABA(A)或GABA(C)受体(GABA(C)Rs或GABA(A)Rs)会使总的NMDAR电荷产生微小变化。当GABA(A)Rs和GABA(C)Rs都被阻断时,开通路中总的NMDAR电荷增加了9倍,关通路中增加了5倍。这揭示了对双极细胞有强烈的GABA(C)R反馈,而这种反馈被由GABA(A)Rs介导的串联无长突细胞突触所抑制。结果表明,NMDAR电流虽大但处于潜伏状态,受到GABA和甘氨酸双重突触前抑制的抑制。这种受控NMDAR激活的一个例子是开和关通路之间的相互作用。阻断开通路会增加关通路中NMDAR的相对强度。刺激延长同样会增加关反应中NMDAR的相对强度。这种NMDAR增强是由GABA和甘氨酸反馈的减少所致。因此,视网膜网络通过突触前去抑制来募集NMDAR通路。