Different ataxin-3 amyloid aggregates induce intracellular Ca(2+) deregulation by different mechanisms in cerebellar granule cells

Biochim Biophys Acta. 2013 Dec;1833(12):3155-3165. doi: 10.1016/j.bbamcr.2013.08.019. Epub 2013 Sep 11.

Abstract

This work aims at elucidating the relation between morphological and physicochemical properties of different ataxin-3 (ATX3) aggregates and their cytotoxicity. We investigated a non-pathological ATX3 form (ATX3Q24), a pathological expanded form (ATX3Q55), and an ATX3 variant truncated at residue 291 lacking the polyQ expansion (ATX3/291Δ). Solubility, morphology and hydrophobic exposure of oligomeric aggregates were characterized. Then we monitored the changes in the intracellular Ca(2+) levels and the abnormal Ca(2+) signaling resulting from aggregate interaction with cultured rat cerebellar granule cells. ATX3Q55, ATX3/291Δ and, to a lesser extent, ATX3Q24 oligomers displayed similar morphological and physicochemical features and induced qualitatively comparable time-dependent intracellular Ca(2+) responses. However, only the pre-fibrillar aggregates of expanded ATX3 (the only variant which forms bundles of mature fibrils) triggered a characteristic Ca(2+) response at a later stage that correlated with a larger hydrophobic exposure relative to the two other variants. Cell interaction with early oligomers involved glutamatergic receptors, voltage-gated channels and monosialotetrahexosylganglioside (GM1)-rich membrane domains, whereas cell interaction with more aged ATX3Q55 pre-fibrillar aggregates resulted in membrane disassembly by a mechanism involving only GM1-rich areas. Exposure to ATX3Q55 and ATX3/291Δ aggregates resulted in cell apoptosis, while ATX3Q24 was substantially innocuous. Our findings provide insight into the mechanisms of ATX3 aggregation, aggregate cytotoxicity and calcium level modifications in exposed cerebellar cells.

Keywords: 2-amino-5-phosphonopentanoic acid; 8-anilino-1-naphthalenesulfonic acid; AMPA-R; ANS; APV; Amyloid aggregate; Ataxin-3; BSA; CGNs; CNQX; Fibril toxicity; GM1; Intracellular Ca(2+) level; JD; N-methyl-d-aspartate receptor; N-terminal Josephin domain; NMDA-R; Oligomer toxicity; SBMA; SCA3; ThT; Thioflavin T; VGCCs; bovine serum albumin; cyano-nitroquinoxaline-dione; monosialotetrahexosylganglioside; rat cerebellar granule neurons; spinobulbar muscular atrophy; spinocerebellar ataxia type 3; voltage-gated calcium channels; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid / toxicity*
  • Animals
  • Apoptosis / drug effects
  • Calcium / metabolism*
  • Calcium Channels / metabolism
  • Cell Membrane / metabolism
  • Cerebellum / cytology*
  • G(M1) Ganglioside / pharmacology
  • Intracellular Space / metabolism*
  • Microscopy, Atomic Force
  • Nerve Tissue Proteins / metabolism*
  • Nerve Tissue Proteins / toxicity*
  • Protein Binding / drug effects
  • Protein Structure, Quaternary
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, AMPA / metabolism
  • Spectrometry, Fluorescence
  • Time Factors

Substances

  • Amyloid
  • Calcium Channels
  • Nerve Tissue Proteins
  • Receptors, AMPA
  • G(M1) Ganglioside
  • Calcium