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Abstract

アルツハイマー病で起こる神経細胞死の新たなターゲット分子の発見 -神経細胞死の新たな分子メカニズム解明による革新的治療法の開発に期待-. 京都大学プレスリリース. 2015-08-14.

Neurodegeneration correlates with Alzheimer's disease (AD) symptoms, but the molecular identities of pathogenic amyloid β-protein (Aβ) oligomers and their targets, leading to neurodegeneration, remain unclear. Amylospheroids (ASPD) are AD patient-derived 10- to 15-nm spherical Aβ oligomers that cause selective degeneration of mature neurons. Here, we show that the ASPD target is neuron-specific Na(+)/K(+)-ATPase α3 subunit (NAKα3). ASPD-binding to NAKα3 impaired NAKα3-specific activity, activated N-type voltage-gated calcium channels, and caused mitochondrial calcium dyshomeostasis, tau abnormalities, and neurodegeneration. NMR and molecular modeling studies suggested that spherical ASPD contain N-terminal-Aβ-derived "thorns" responsible for target binding, which are distinct from low molecular-weight oligomers and dodecamers. The fourth extracellular loop (Ex4) region of NAKα3 encompassing Asn(879) and Trp(880) is essential for ASPD-NAKα3 interaction, because tetrapeptides mimicking this Ex4 region bound to the ASPD surface and blocked ASPD neurotoxicity. Our findings open up new possibilities for knowledge-based design of peptidomimetics that inhibit neurodegeneration in AD by blocking aberrant ASPD-NAKα3 interaction.

Journal

  • Proceedings of the National Academy of Sciences of the United States of America

    Proceedings of the National Academy of Sciences of the United States of America 112(32), E4465-E4474, 2015-08-11

    National Academy of Sciences

Codes

  • NII Article ID (NAID)
    120005647505
  • NII NACSIS-CAT ID (NCID)
    AA00786025
  • Text Lang
    ENG
  • Article Type
    journal article
  • ISSN
    1091-6490
  • Data Source
    IR 
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