Figure 7
Figure 7. Positive signaling feedback between VEGFR2 and Rap1b modulates EC responses to VEGF stimulation: a model. Rap1b acts upstream from VEGFR2 by regulating the activity of integrin αvβ3 and thus feeding into integrin αvβ3 signaling to VEGFR2. There is a reciprocal up-regulation of Rap1b and integrin β3 in the absence of either protein (Figure 3E and supplemental Figure 5B), further suggesting the existence of a feedback mechanism between the two proteins. Because inhibition of Rap1b in integrin β3−/− ECs leads to a further inhibition of VEGFR2 activation, other mediators of Rap1b regulation of VEGFR2 exist beside integrin β3, however, they do not involve integrin α5β1. Rap1b also acts downstream from VEGFR2, as it becomes rapidly and transiently activated by VEGF.18 This creates a positive signaling feedback between Rap1b and VEGFR2 which promotes VEGF-induced blood vessel formation in vivo and EC responses in vitro; responses that are inhibited in mouse Rap1b-ECKO, zebrafish rap1b morphants and Rap1b−/− ECs, respectively.

Positive signaling feedback between VEGFR2 and Rap1b modulates EC responses to VEGF stimulation: a model. Rap1b acts upstream from VEGFR2 by regulating the activity of integrin αvβ3 and thus feeding into integrin αvβ3 signaling to VEGFR2. There is a reciprocal up-regulation of Rap1b and integrin β3 in the absence of either protein (Figure 3E and supplemental Figure 5B), further suggesting the existence of a feedback mechanism between the two proteins. Because inhibition of Rap1b in integrin β3−/− ECs leads to a further inhibition of VEGFR2 activation, other mediators of Rap1b regulation of VEGFR2 exist beside integrin β3, however, they do not involve integrin α5β1. Rap1b also acts downstream from VEGFR2, as it becomes rapidly and transiently activated by VEGF.18  This creates a positive signaling feedback between Rap1b and VEGFR2 which promotes VEGF-induced blood vessel formation in vivo and EC responses in vitro; responses that are inhibited in mouse Rap1b-ECKO, zebrafish rap1b morphants and Rap1b−/− ECs, respectively.

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