Glial loss of the metallo β-lactamase domain containing protein, SWIP-10, induces age- and glutamate-signaling dependent, dopamine neuron degeneration

Chelsea L. Gibson, Joseph T. Balbona, Ashlin Niedzwiecki, Peter Rodriguez, Ken C.Q. Nguyen, David H. Hall, Randy D. Blakely

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Across phylogeny, glutamate (Glu) signaling plays a critical role in regulating neural excitability, thus supporting many complex behaviors. Perturbed synaptic and extrasynaptic Glu homeostasis in the human brain has been implicated in multiple neuropsychiatric and neurodegenerative disorders including Parkinson’s disease, where theories suggest that excitotoxic insults may accelerate a naturally occurring process of dopamine (DA) neuron degeneration. In C. elegans, mutation of the glial expressed gene, swip-10, results in Glu-dependent DA neuron hyperexcitation that leads to elevated DA release, triggering DA signaling-dependent motor paralysis. Here, we demonstrate that swip-10 mutations induce premature and progressive DA neuron degeneration, with light and electron microscopy studies demonstrating the presence of dystrophic dendritic processes, as well as shrunken and/or missing cell soma. As with paralysis, DA neuron degeneration in swip-10 mutants is rescued by glial-specific, but not DA neuron-specific expression of wildtype swip-10, consistent with a cell non-autonomous mechanism. Genetic studies implicate the vesicular Glu transporter VGLU-3 and the cystine/Glu exchanger homolog AAT-1 as potential sources of Glu signaling supporting DA neuron degeneration. Degeneration can be significantly suppressed by mutations in the Ca2+permeable Glu receptors, nmr-2 and glr-1, in genes that support intracellular Ca2+signaling and Ca2+-dependent proteolysis, as well as genes involved in apoptotic cell death. Our studies suggest that Glu stimulation of nematode DA neurons in early larval stages, without the protective actions of SWIP-10, contributes to insults that ultimately drive DA neuron degeneration. The swip-10 model may provide an efficient platform for the identification of molecular mechanisms that enhance risk for Parkinson’s disease and/or the identification of agents that can limit neurodegenerative disease progression.

Original languageEnglish (US)
Article numbere1007269
JournalPLoS Genetics
Volume14
Issue number3
DOIs
StatePublished - Mar 1 2018

Fingerprint

Nerve Degeneration
Dopaminergic Neurons
neuroglia
dopamine
Neuroglia
glutamates
Glutamic Acid
neurons
mutation
protein
gene
proteins
homeostasis
electron microscopy
Paralysis
Neurodegenerative Diseases
Mutation
Parkinson disease
nematode
Parkinson Disease

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Cancer Research

Cite this

Glial loss of the metallo β-lactamase domain containing protein, SWIP-10, induces age- and glutamate-signaling dependent, dopamine neuron degeneration. / Gibson, Chelsea L.; Balbona, Joseph T.; Niedzwiecki, Ashlin; Rodriguez, Peter; Nguyen, Ken C.Q.; Hall, David H.; Blakely, Randy D.

In: PLoS Genetics, Vol. 14, No. 3, e1007269, 01.03.2018.

Research output: Contribution to journalArticle

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