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In the nervous system, guidance molecules called semaphorins bind to receptors called plexins to induce motility and regulate axonal pathfinding. Now, Swiercz et al. (page 869) show that plexin-B1, after binding its ligand semaphorin 4D (Sema4D), forms a heterodimer with the tyrosine kinase ErbB2. This raises the intriguing possibility that the semaphorins and the EGF-like ligands of ErbB receptors may affect each other's signaling abilities.
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Swiercz et al. used a number of different kinase inhibitors to block the RhoA activation seen downstream of Sema4D binding to plexin-B1. These findings revealed that one or more proteins in the ErbB family was involved. Of the four members of the ErbB family, only a dominant-negative ErbB2 mutant showed significant effects on RhoA activation. Unlike other family members, ErbB2 is not activated by a ligand. Rather it acts in trans via association with other tyrosine kinases. Likewise, Swiercz et al. found that plexin-B1 and ErbB2 form a heterodimer in which activated ErbB2 phosphorylates plexin-B1. This phosphorylation is required for plexin-B1 signaling via PDZ-RhoGEF/LARG to RhoA.
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. w8 H; p% I y5 dCompetition experiments between Sema4D and EGF (which stimulates and activates ErbB1/ErbB2 heterodimers) resulted in an overall inhibition of plexin-B–mediated signaling by EGF. But, at the same time, Sema4D is able to activate the ErbB2 pathway, which may under some circumstances lead to tumor promotion.(ErbB2 (red) on axons is phosphorylated () |
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发表于 2009-3-6 08:25
发表于 2015-6-7 20:10
