Abstract

Apoptosis plays a major role in development, tissue renewal and the progression of degenerative diseases. Studies on various types of mammalian cells reported a pro-apoptotic function of acetylcholinesterase (AChE), particularly in the formation of the apoptosome and the degradation of nuclear DNA. While three AChE splice variants are present in mammals, invertebrates typically express two ache genes that code for a synaptically located protein and a protein with non-synaptic functions respectively. In order to investigate a potential contribution of AChE to apoptosis in insects, we selected the migratory locust Locusta migratoria. We established primary neuronal cultures of locust brains and characterized apoptosis progression in vitro. Dying neurons displayed typical characteristics of apoptosis, including caspase-activation, nuclear condensation and DNA fragmentation visualized by TUNEL staining. Addition of the AChE inhibitors neostigmine and territrem B reduced apoptotic cell death under normal culture conditions. Moreover, both inhibitors completely suppressed hypoxia-induced neuronal cell death. Exposure of live animals to severe hypoxia moderately increased the expression of ace-1 in locust brains in vivo. Our results indicate a previously unreported role of AChE in insect apoptosis that parallels the pro-apoptotic role in mammalian cells. This similarity adds to the list of apoptotic mechanisms shared by mammals and insects, supporting the hypothesized existence of an ancient, complex apoptosis regulatory network present in common ancestors of vertebrates and insects.

Highlights

  • Apoptosis describes highly regulated processes that lead to death and elimination of individual cells with little or no negative impact on the surrounding tissue

  • These results indicate that AChE promotes apoptosis in locusts, as it has previously been described for mammalian cells

  • In order to characterize hypoxia-induced death of locust neurons as apoptotic, primary neuron cultures were subjected to cleaved-caspase-3 immunostaining, DNA labelling with DAPI and transferase dUTP nick end labelling (TUNEL) stainings

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Summary

Introduction

Apoptosis describes highly regulated processes that lead to death and elimination of individual cells with little or no negative impact on the surrounding tissue. Apoptosis is characterized by loss of cellular volume, condensation of nuclear chromatin due to DNA fragmentation, plasma membrane blebbing and formation of apoptotic bodies. Caspases that mediate the final stages of apoptosis cleave various selected substrates, either to destabilize or degrade structural elements of the cell or to activate executors of downstream apoptotic processes [9, 10] (Fig. 1). This may imply sequential activation of initiator caspases and executioner caspases (caspase-9 and caspase-3 in vertebrates; dronc and drice in D. melanogaster) or direct

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