Abstract

A fluorescent triple staining method was developed to stain the cytoplasm of neurons red, the nuclei of all kinds of cells, including neurons, blue and the nuclei of apoptotic neurons in cyan in the twelve ventral ganglia (VG) of the Bombyx mori ventral nerve cord. This differential staining method was used to distinguish between apoptotic and normal neurons in the suboesophageal ganglion (SOG), thoracic ganglia (TG)1 to TG3 and abdominal ganglia (AG)1 to AG8 and also determine the changes in the num- bers of apoptotic neurons that occur during postembryonic development. In most of the VG tested, neuronal apoptosis was most marked during the period from the end of larval life to the mid pupal stage. The greatest number of apoptotic neurons was found in SOG of day-5 pupae, TG1 to TG3 and AG1 to AG4 of day-1 pupae, and AG5 to AG8 of day-4 pupae. In vivo injection of 20- hydroxyecdysone (20E) into day-8 5th instar larvae resulted in both a considerable increase in the number of apoptotic neurons and cleavage of procaspase-3 into caspase-3, which induced neuronal apoptosis in SOG and AG6 to AG8 in day-1 pupae, and a slight increase in the number of apoptotic neurons in TG1. In TG3 and AG4, however, it had little effect on the number of apoptotic neu- rons or cleavage of procaspase-3. Treatment of the VG of both day-8 5th instar larvae and day-2 pupae with protein synthesis inhibi- tors by in vivo injection triggered a significant inhibition of neuronal apoptosis and procaspase-3 cleavage in most of these ganglia in day-1 pupae and day-4 pupae, but not TG3 and AG4, in which there was little procaspase-3 and caspase-3. In vivo injection of caspase-8 and -3 inhibitors into day-8 5th instar larvae and day-2 pupae led to a substantial inhibition of neuronal apoptosis and of procaspase-3 cleavage in SOG, AG6 and TAG, but not in TG3 or AG4 of day-1 pupae and day-4 pupae. These findings suggest that neurons that die in SOG, TG1 and AG6 to AG8 in day-1 and -4 pupae may undergo apoptosis induced by the synthesis of a new pro- tein and caspase-8- and -3-implicated signal transduction by the increase in titre of 20E in the haemolymph but not the neuronal aopotosis in TG3 and AG4. This study provides neurobiologists with valuable information and a means of studying neuronal apop- tosis in the nervous system of insects.

Highlights

  • The central nervous system (CNS) of insects consists of the ventral nerve cord (VNC) and the brain (Bate & Martinez-Arias, 1993)

  • Simple fluorescent triple staining method was used to differentially stain non-neuronal, normal neuronal and apoptotic neuronal cells in twelve ganglia of the VNC at different stages in development from the day-1 1st instar larval stage up to day-1 adults. This method was developed using AG7 and employed anti-Horseradish peroxidase (HRP) conjugated with Cy3 to stain the neuronal cytoplasm, DAPI to stain the nuclei of all the cells and deoxyuridine 5'-triphosphate (dUTP) conjugated with FITC to stain only the fragmented ends of DNA

  • Apoptotic neurons had a red cytoplasm and blue nuclei when stained with Cy3 and DAPI, but the color of their nuclei was cyan when stained with both nuclear DAPI and FITC

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Summary

Introduction

The central nervous system (CNS) of insects consists of the ventral nerve cord (VNC) and the brain (Bate & Martinez-Arias, 1993). A reduction in the length of the connections between ganglia in B. mori leads to ganglionic fusion in the pupal stages: fusion of SOG into the brain, fusion of AG1 and AG2 into TG1 and TG2, and incorporation of AG6 into AG7/8 (Sato, 1998; Yamanaka et al, 2000; Hirashima et al, 2007; Mitsumasu et al, 2008). These ganglionic fusions are complete by day-4 of pupation. Most specific numerical changes in the neurons in the ventral ganglia (VG) of the VNC, including programmed cell death (PCD), or apoptosis, occur during metamorphosis (Truman & Schwartz, 1984)

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