論文

査読有り
2011年5月

Syntaxin 1B Suppresses Macropinocytosis and Semaphorin 3A-Induced Growth Cone Collapse

JOURNAL OF NEUROSCIENCE
  • Hiroyuki Kabayama
  • ,
  • Makoto Takeuchi
  • ,
  • Masahiko Taniguchi
  • ,
  • Naoko Tokushige
  • ,
  • Shunji Kozaki
  • ,
  • Akihiro Mizutani
  • ,
  • Takeshi Nakamura
  • ,
  • Katsuhiko Mikoshiba

31
20
開始ページ
7357
終了ページ
7364
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1523/JNEUROSCI.2718-10.2011
出版者・発行元
SOC NEUROSCIENCE

Growth cone collapse is a crucial process for repulsive axon guidance and is accompanied by a reduction in growth cone surface area. This process of reduction may be regulated by endocytosis; however, its molecular mechanism is unclear. Macropinocytosis is a clathrin-independent form of endocytosis in which large areas of plasma membrane can be engulfed. We have reported previously that macropinocytosis is induced in growth cones of chick dorsal root ganglion neurons by semaphorin 3A (Sema3A), a repulsive axon guidance cue, and that Sema3A-induced reduction in growth cone surface area and macropinocytic vacuole area were correlated, suggesting a positive role for macropinocytosis in Sema3A-induced growth cone collapse. In the present study, we found that syntaxin 1B (Syx1B), a membrane trafficking protein, is a negative regulator of macropinocytosis, and its expression is downregulated by Sema3A signaling. Macropinocytosis inhibitor ethylisopropylamiloride or Syx1B overexpression suppressed Sema3A-induced macropinocytosis and growth cone collapse. These results indicate that Syx1B couples macropinocytosis-mediated massive internalization of the plasma membrane to Sema3A-induced growth cone collapse.

リンク情報
DOI
https://doi.org/10.1523/JNEUROSCI.2718-10.2011
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/21593320
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000290716600015&DestApp=WOS_CPL
ID情報
  • DOI : 10.1523/JNEUROSCI.2718-10.2011
  • ISSN : 0270-6474
  • PubMed ID : 21593320
  • Web of Science ID : WOS:000290716600015

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