論文

査読有り
2005年2月

Involvement of the phosphatidylinositol 3-kinase/Rac1 and cdc42 pathways in radial migration of cortical neurons

JOURNAL OF BIOLOGICAL CHEMISTRY
  • D Konno
  • ,
  • S Yoshimura
  • ,
  • K Hori
  • ,
  • H Maruoka
  • ,
  • K Sobue

280
6
開始ページ
5082
終了ページ
5088
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1074/jbc.M408251200
出版者・発行元
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

During cortical development, newly generated neurons migrate radially toward their final positions. Although several candidate genes essential for this radial migration have been reported, the signaling pathways regulating it are largely unclear. Here we studied the role of phosphatidylinositol (PI) 3-kinase and its downstream signaling molecules in the radial migration of cortical neurons in vivo and in vitro. The expression of constitutively active and dominant-negative PI 3-kinases markedly inhibited radial migration. In the neocortical slice culture, a PI 3-kinase inhibitor suppressed the formation of GTP-bound Rac1 and Cdc42 and radial migration. Constitutively active and dominant-negative forms of Rac1 and Cdc42 but not Akt also significantly inhibited radial migration. In migrating neurons, wild-type Rac1 and Cdc42 showed different localizations; Rac1 localized to the plasma membrane and Cdc42 to the perinuclear region on the side of the leading processes. These results suggest that both the PI 3-kinase/Rac1 and Cdc42 pathways are involved in the radial migration of cortical neurons and that they have different roles.

リンク情報
DOI
https://doi.org/10.1074/jbc.M408251200
CiNii Articles
http://ci.nii.ac.jp/naid/80017205207
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/15557338
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000227096600130&DestApp=WOS_CPL
ID情報
  • DOI : 10.1074/jbc.M408251200
  • ISSN : 0021-9258
  • eISSN : 1083-351X
  • CiNii Articles ID : 80017205207
  • PubMed ID : 15557338
  • Web of Science ID : WOS:000227096600130

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