The LRRK2 G2019S mutation alters astrocyte-to-neuron communication via extracellular vesicles and induces neuron atrophy in a human iPSC-derived model of Parkinson's disease

Elife. 2021 Sep 30:10:e73062. doi: 10.7554/eLife.73062.

Abstract

Astrocytes are essential cells of the central nervous system, characterized by dynamic relationships with neurons that range from functional metabolic interactions and regulation of neuronal firing activities, to the release of neurotrophic and neuroprotective factors. In Parkinson's disease (PD), dopaminergic neurons are progressively lost during the course of the disease, but the effects of PD on astrocytes and astrocyte-to-neuron communication remain largely unknown. This study focuses on the effects of the PD-related mutation LRRK2 G2019S in astrocytes generated from patient-derived induced pluripotent stem cells. We report the alteration of extracellular vesicle (EV) biogenesis in astrocytes and identify the abnormal accumulation of key PD-related proteins within multivesicular bodies (MVBs). We found that dopaminergic neurons internalize astrocyte-secreted EVs and that LRRK2 G2019S EVs are abnormally enriched in neurites and fail to provide full neurotrophic support to dopaminergic neurons. Thus, dysfunctional astrocyte-to-neuron communication via altered EV biological properties may participate in the progression of PD.

Keywords: Parkinson's disease; cell biology; exosomes; human; mouse; neurodegeneration; neurodegenerative diseases; neuron-glia interactions; neuroscience; non-cell autonomous.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / enzymology*
  • Astrocytes / ultrastructure
  • Atrophy
  • Case-Control Studies
  • Cell Communication*
  • Cell Line
  • Dopaminergic Neurons / enzymology*
  • Dopaminergic Neurons / pathology
  • Endocytosis
  • Exosomes / enzymology*
  • Exosomes / genetics
  • Exosomes / ultrastructure
  • Humans
  • Induced Pluripotent Stem Cells / enzymology*
  • Induced Pluripotent Stem Cells / ultrastructure
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / genetics
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutation
  • Neural Stem Cells / enzymology*
  • Neural Stem Cells / ultrastructure
  • Organelle Biogenesis
  • Parkinson Disease / enzymology*
  • Parkinson Disease / genetics
  • Parkinson Disease / pathology

Substances

  • LRRK2 protein, human
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

Associated data

  • GEO/GSE152768