Arsenic induces accumulation of α-synuclein: Implications for synucleinopathies and neurodegeneration

Aram B. Cholanians, Andy V. Phan, Eric J. Ditzel, Todd D Camenisch, Serrine Lau, Terrence Monks

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Synucleinopathies, including Parkinson's disease (PD), are neurodegenerative diseases characterized by accumulation of α-synuclein (SYN), a small neuronal protein with prion like properties that plays a central role in PD pathogenesis. SYN can misfold and generate toxic oligomers/aggregates, which can be cytotoxic. Environmental arsenic (As)-containing pesticide use correlates with increased incidence of PD. Moreover, because As exposure can lead to inhibition of autophagic flux we hypothesize that As can facilitate the accumulation of toxic SYN oligomers/aggregates and subsequent increases in markers of autophagy. We therefore examined the role of As in the oligomerization of SYN, and the consequences thereof. Chronic exposure of SH-SY5Y cells overexpressing SYN to As caused a dose-dependent oligomerization of SYN, with concomitant increases in protein ubiquitination and expression of other stress markers (protein glutathione binding, γ-GCS, light chain 3 (LC3)-I/II, P62, and NAD(P)H dehydrogenase quinone 1), indicative of an increased proteotoxic stress. Immunocytochemical analyses revealed an accumulation of SYN, and it's colocalization with LC3, a major autophagic protein. Mice exposed to As (100 ppb) for 1 month, exhibited elevated SYN accumulation in the cortex and striatum, and elevations in protein ubiquitination and LC3-I and II levels. However, tyrosine hydroxylase (TH), an indicator of dopaminergic cell density, was upregulated in the As exposed animals. Because SYN can inhibit TH function, and As can decrease monoamine levels, As exposure possibly leads to compensatory mechanisms leading to an increase in TH expression. Our findings suggest that susceptible individuals may be at higher risk of developing synucleinopathies and/or neurodegeneration due to environmental As exposure.

Original languageEnglish (US)
Article numberkfw117
Pages (from-to)271-281
Number of pages11
JournalToxicological Sciences
Volume153
Issue number2
DOIs
StatePublished - Oct 1 2016

Fingerprint

Synucleins
Arsenic
Tyrosine 3-Monooxygenase
Parkinson Disease
Oligomerization
Poisons
Ubiquitination
Proteins
Oligomers
Light
Neurodegenerative diseases
NAD(P)H Dehydrogenase (Quinone)
Prions
Autophagy
Environmental Exposure
Heat-Shock Proteins
Pesticides
Protein Binding
Neurodegenerative Diseases
Glutathione

Keywords

  • Arsenic
  • Autophagy
  • Parkinson's disease
  • α-synuclein

ASJC Scopus subject areas

  • Toxicology

Cite this

Arsenic induces accumulation of α-synuclein : Implications for synucleinopathies and neurodegeneration. / Cholanians, Aram B.; Phan, Andy V.; Ditzel, Eric J.; Camenisch, Todd D; Lau, Serrine; Monks, Terrence.

In: Toxicological Sciences, Vol. 153, No. 2, kfw117, 01.10.2016, p. 271-281.

Research output: Contribution to journalArticle

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