Misc.

Open access
Feb 15, 2004

Dual roles of Sema6D in cardiac morphogenesis through region-specific association of its receptor, Plexin-A1, with off-track and vascular endothelial growth factor receptor type 2

Genes and Development
  • Toshihiko Toyofuku
  • Hong Zhang
  • Atsushi Kumanogoh
  • Noriko Takegahara
  • Fumikazu Suto
  • Junko Kamei
  • Kazuhiro Aoki
  • Masanori Yabuki
  • Masatsugu Hori
  • Hajime Fujisawa
  • Hitoshi Kikutani
  • Display all

Volume
18
Number
4
First page
435
Last page
447
Language
English
Publishing type
DOI
10.1101/gad.1167304
Publisher
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT

Semaphorins, originally identified as axon guidance factors in the nervous system, play integral roles in organogenesis. Here, we demonstrate a critical involvement of Sema6D in cardiac morphogenesis. Ectopic expression of Sema6D or RNA interference against Sema6D induces expansion or narrowing of the ventricular chamber, respectively, during chick embryonic development. Sema6D also exerts region-specific activities on cardiac explants, a migration-promoting activity on outgrowing cells from the conotruncal segment, and a migration-inhibitory activity on those from the ventricle. Plexin-A1 mediates these activities as the major Sema6D-binding receptor. Plexin-A1 forms a receptor complex with vascular endothelial growth factor receptor type 2 in the conotruncal segment or with Off-track in the ventricle segment; these complexes are responsible for the effects of Sema6D on the respective regions. Thus, the differential association of Plexin-A1 with additional receptor components entitles Sema6D to exert distinct biological activities at adjacent regions. This is crucial for complex cardiac morphogenesis.

Link information
DOI
https://doi.org/10.1101/gad.1167304
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/14977921
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000220100100009&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=12144285611&origin=inward Open access
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=12144285611&origin=inward
ID information
  • DOI : 10.1101/gad.1167304
  • ISSN : 0890-9369
  • Pubmed ID : 14977921
  • SCOPUS ID : 12144285611
  • Web of Science ID : WOS:000220100100009

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