Inhibition of clathrin-mediated endocytosis prevents amyloid β-induced axonal damage

Tomoharu Kuboyama*, Young A. Lee, Hiroaki Nishiko, Chihiro Tohda

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

23 被引用数 (Scopus)

抄録

Amyloid β (Aβ)-induced axonal degeneration is a major cause of Alzheimer's disease (AD) pathology. However, the critical target to prevent Aβ-induced axonal degeneration remains unknown. Here, we analyzed growth cone collapse elicited by Aβ, a putative early Aβ-induced event in axons. Although no study has yet shown influence of Aβ on the growth cone, we first visualized Aβ-initiated growth cone collapse in cultured neurons. Furthermore, we determined that the collapse was triggered by clathrin-mediated endocytosis probably via Aβ-Ca2+ signaling. The inhibition of clathrin-mediated endocytosis prevented Aβ-induced axonal loss both invitro and invivo and prevented memory impairment in an AD mouse model. Our results clarified the important role of clathrin-mediated endocytosis in Aβ-induced collapse of growth cone that leads to axonal degeneration and memory impairment.

本文言語英語
ページ(範囲)1808-1819
ページ数12
ジャーナルNeurobiology of Aging
36
5
DOI
出版ステータス出版済み - 2015

ASJC Scopus 主題領域

  • 神経科学一般
  • 加齢科学
  • 臨床神経学
  • 発生生物学
  • 老年医学

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