Different ataxin-3 amyloid aggregates induce intracellular Ca2+ deregulation by different mechanisms in cerebellar granule cells

作者：Pellistri Francesca; Bucciantini Monica^*; Invernizzi Gaetano; Gatta Elena; Penco Amanda; Frana Anna Maria; Nosi Daniele; Relini Annalisa; Regonesi Maria Elena; Gliozzi Alessandra; Tortora Paolo; Robello Mauro; Stefani Massimo

来源：Biochimica et Biophysica Acta-Molecular Cell Research, 2013, 1833(12): 3155-3165.

DOI：10.1016/j.bbamcr.2013.08.019

• Ataxin-3
• Amyloid aggregate
• Intracellular Ca2+ level
• Oligomer toxicity
• Fibril toxicity

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 (ATY3Q24), a pathological expanded form (ATX3Q55), and an ATX3 variant truncated at residue 291 lacking the polyQ expansion (ATX3/291 Delta). Solubility, morphology and hydrophobic exposure of oligomeric aggregates were characterized. Then we monitored the changes in the intracellular Ca2+ levels and the abnormal Ca2+ signaling resulting from aggregate interaction with cultured rat cerebellar granule cells. ATX3Q55, ATX3/291 Delta and, to a lesser extent, ATX3Q24 oligomers displayed similar morphological and physicochemical features and induced qualitatively comparable time-dependent intracellular Ca2+ responses. However, only the pre-fibrillar aggregates of expanded ATX3 (the only variant which forms bundles of mature fibrils) triggered a characteristic Ca2+ 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 A1X3Q55 and ATX3/291 Delta 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.

• 出版日期2013-12