Abstract

Zebrafish larval gut could be considered as an excellent model to study functions of vertebrate digestive organs, by virtue of its simplicity and transparency as well as the availability of mutants. However, there has been scant investigation of the detailed behavior of muscular and enteric nervous systems to convey bolus, an aggregate of digested food. Here we visualized peristalsis using transgenic lines expressing a genetically encoded Ca2+ sensor in the circular smooth muscles. An intermittent Ca2+ signal cycle was observed at the oral side of the bolus, with Ca2+ waves descending and ascending from there. We also identified a regular cycle of weaker movement that occurs regardless of the presence or absence of bolus, corresponding likely to slow waves. Direct photo-stimulation of circular smooth muscles expressing ChR2 could cause local constriction of the gut, while the stimulation of a single or a few neurons could cause the local induction or arrest of gut movements. These results indicate that the larval gut of zebrafish has basic features found in adult mammals despite the small number of enteric neurons, providing a foundation for the study, at the single-cell level in vivo, in controlling the gut behaviors in vertebrates.

Highlights

  • Zebrafish larval gut could be considered as an excellent model to study functions of vertebrate digestive organs, by virtue of its simplicity and transparency as well as the availability of mutants

  • The bolus, once swallowed, is conveyed through the gut to the anus. This movement, peristalsis, is achieved by two sets of muscular systems. These systems are regulated by neuronal groups of the enteric nervous system (ENS), which is derived from the neural c­ rest[1]

  • Using Hu immunohistochemistry, about 380 enteric neuron cell bodies per wild-type intestine were identified at 5 days post-fertilization[9] and about 700 were identified at 8 dpf

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Summary

Introduction

Zebrafish larval gut could be considered as an excellent model to study functions of vertebrate digestive organs, by virtue of its simplicity and transparency as well as the availability of mutants. Movement, we fed larvae with paramecium from 5 dpf and performed C­ a2+ imaging of the gut at 8 dpf of SAGFF(LF)134A; Tg(UAS: GCaMP3) from the lateral side. We found strong ­Ca2+ events in the circular smooth muscles during peristaltic movement in 7 out of 10 larvae.

Results
Conclusion
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