Characterization of a novel stimulus-induced glial calcium wave in Drosophila larval peripheral segmental nerves and its role in PKG-modulated thermoprotection

J Neurogenet. 2021 Sep;35(3):221-235. doi: 10.1080/01677063.2021.1941945. Epub 2021 Jul 26.

Abstract

Insects, as poikilotherms, have adaptations to deal with wide ranges in temperature fluctuation. Allelic variations in the foraging gene that encodes a cGMP dependent protein kinase, were discovered to have effects on behavior in Drosophila by Dr. Marla Sokolowski in 1980. This single gene has many pleiotropic effects and influences feeding behavior, metabolic storage, learning and memory and has been shown to affect stress tolerance. PKG regulation affects motoneuronal thermotolerance in Drosophila larvae as well as adults. While the focus of thermotolerance studies has been on the modulation of neuronal function, other cell types have been overlooked. Because glia are vital to neuronal function and survival, we wanted to determine if glia play a role in thermotolerance as well. In our investigation, we discovered a novel calcium wave at the larval NMJ and set out to characterize the wave's dynamics and the potential mechanism underlying the wave prior to determining what effect, if any, PKG modulation has on the thermotolerance of glia cells. Using pharmacology, we determined that calcium buffering mechanisms of the mitochondria and endoplasmic reticulum play a role in the propagation of our novel glial calcium wave. By coupling pharmacology with genetic manipulation using RNA interference (RNAi), we found that PKG modulation in glia alters thermoprotection of function as well as glial calcium wave dynamics.

Keywords: 3rd instar larvae; Drosophila melanogaster; NMJ; PKG; RNAi; calcium; endoplasmic reticulum; foraging; glia; mitochondria; peripheral nervous system; thermotolerance.

MeSH terms

  • Animals
  • Body Temperature Regulation / physiology*
  • Calcium Signaling / physiology*
  • Cyclic GMP-Dependent Protein Kinases / metabolism*
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / physiology*
  • Neuroglia / metabolism*
  • Neuromuscular Junction / metabolism

Substances

  • Drosophila Proteins
  • Cyclic GMP-Dependent Protein Kinases
  • for protein, Drosophila