Firing-rate Mode Segregation by Neural Circuit Polarization

2021 ◽  
pp. 159-171
Keyword(s):  
2018 ◽  
Author(s):  
Wei-Hsiang Lin ◽  
Richard A. Baines

Abstract (174 words)Pumilio (Pum) is a key component of neuron firing-rate homeostasis that maintains stability of neural circuit activity. Whilst Pum is ubiquitously expressed, we understand little about how synaptic excitation regulates its expression. Here, we characterised the Drosophila dpum promoter and identified multiple Myocyte enhancer factor-2 (Mef2)-binding elements. To understand the transactivation capability of dMef2, we cloned 12 dmef2 splice variants and used a luciferase-based assay to monitor dpum promoter activity. Whilst all 12 dMef2 splice variants enhance dpum promoter activity, exon 10-containing variants induce greater transactivation. Previous work shows dPum expression increases with synaptic excitation. However, we observe no change in dmef2 transcript in CNS exposed to picrotoxin (PTX). The lack of activity-dependence is indicative of additional regulation. We identified p300 as a likely candidate. We show that by binding to dMef2, p300 represses dpum transactivation. Significantly, p300 transcript is down-regulated by enhanced synaptic excitation (PTX) which, in turn, increases transcription of dpum through derepression of dMef2. These results suggest the activity-dependent expression of dpum is regulated by an interaction between p300 and dMef2.


2014 ◽  
Vol 112 (9) ◽  
pp. 2302-2315 ◽  
Author(s):  
Ahmed Z. Obeidat ◽  
Paul Nardelli ◽  
Randall K. Powers ◽  
Timothy C. Cope

Recent reports show that synaptic inhibition can modulate postsynaptic spike timing without having strong effects on firing rate. Thus synaptic inhibition can achieve multiplicity in neural circuit operation through variable modulation of postsynaptic firing rate vs. timing. We tested this possibility for recurrent inhibition (RI) of spinal motoneurons. In in vivo electrophysiological studies of adult Wistar rats anesthetized by isoflurane, we examined repetitive firing of individual lumbosacral motoneurons recorded in current clamp and modulated by synchronous antidromic electrical stimulation of multiple motor axons and their centrally projecting collateral branches. Antidromic stimulation produced recurrent inhibitory postsynaptic potentials (RIPSPs) having properties similar to those detailed in the cat. Although synchronous RI produced marked short-term modulation of motoneuron spike timing and instantaneous firing rate, there was little or no suppression of average firing rate. The bias in firing modulation of timing over average rate was observed even for high-frequency RI stimulation (100 Hz), perhaps because of the brevity of RIPSPs, which were more than twofold shorter during motoneuron firing compared with rest. These findings demonstrate that RI in the mammalian spinal cord has the capacity to support and not impede heightened motor pool activity, possibly during rapid, forceful movements.


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