Abstract

Nitric oxide is a bioactive signalling molecule that is known to affect a wide range of neurodevelopmental processes. However, its functional relevance to neuromuscular development is not fully understood. Here we have examined developmental roles of nitric oxide during formation and maturation of neuromuscular contacts in zebrafish. Using histochemical approaches we show that elevating nitric oxide levels reduces the number of neuromuscular synapses within the axial swimming muscles whilst inhibition of nitric oxide biosynthesis has the opposite effect. We further show that nitric oxide signalling does not change synapse density, suggesting that the observed effects are a consequence of previously reported changes in motor axon branch formation. Moreover, we have used in vivo patch clamp electrophysiology to examine the effects of nitric oxide on physiological maturation of zebrafish neuromuscular junctions. We show that developmental exposure to nitric oxide affects the kinetics of spontaneous miniature end plate currents and impacts the neuromuscular drive for locomotion. Taken together, our findings implicate nitrergic signalling in the regulation of zebrafish neuromuscular development and locomotor maturation.

Highlights

  • Nitric oxide (NO) is a signalling molecule that regulates synaptogenesis in both central and peripheral nervous tissue [1,2,3,4,5,6,7,8]

  • Since our previous work suggested that NO/cyclic guanosine monophosphate (cGMP) signalling affects motor axon branch formation without impairing motor root growth, we segregated puncta into two domains: those located on the motor axon fascicle and those located on motor axon branches (Figure 1A)

  • The main findings of this study are that developmental manipulation of NO signalling reduces the number of neuromuscular synapses and affects the physiological properties of neuromuscular junction (NMJ) within the developing muscle population of zebrafish embryos

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Summary

Introduction

Nitric oxide (NO) is a signalling molecule that regulates synaptogenesis in both central and peripheral nervous tissue [1,2,3,4,5,6,7,8]. Developmental inhibition of NO/cGMP activity markedly increases the number of collaterals formed on motor axons over the first three days of development whereas exogenous exposure to either NO donors or cGMP analogs has the opposite effect [41]. Whilst these observations strongly suggest that NO/cGMP signalling influences zebrafish motor axon development, the consequences to NMJ maturation remain poorly understood

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