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XB-ART-40568
J Neurosci November 4, 2009; 29 (44): 13981-91.

Retinotopic mapping requires focal adhesion kinase-mediated regulation of growth cone adhesion.

Woo S , Rowan DJ , Gomez TM .


Abstract
Adhesion controls growth cone motility, yet the effects of axon guidance cues on adhesion site dynamics are poorly understood. Here we show that ephrin-A1 reduces retinal ganglion cell (RGC) axon outgrowth by stabilizing existing adhesions and inhibiting new adhesion assembly. Ephrin-A1 activates focal adhesion kinase (FAK) in an integrin- and Src-dependent manner and the effects of ephrin-A1 on growth cone motility require FAK activation. We also find that FAK is expressed in a high temporal to low nasal gradient in RGCs, similar to EphA receptors, and that balanced FAK activation is necessary for optimal axon outgrowth. Last, we find that FAK is required for proper topographic positioning of retinal axons along the anterior-posterior axis of the optic tectum in both Xenopus and zebrafish, a guidance decision mediated in part by A-type ephrins. Together, our data suggest that ephrin-A1 controls growth cone advance by modulating adhesive point contacts through FAK activation and that graded FAK signaling is an important component of ephrin-A-mediated retinotopic mapping.

PubMed ID: 19890008
PMC ID: PMC2796108
Article link: J Neurosci
Grant support: [+]
Genes referenced: actl6a efna1 isl1 myc pou4f3 ptk2
Morpholinos: ptk2 MO4


Article Images: [+] show captions
References [+] :
Bourgin, The EphA4 receptor regulates dendritic spine remodeling by affecting beta1-integrin signaling pathways. 2007, Pubmed


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