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Adhesion stimulates Scar/WAVE phosphorylation in mammalian cells

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dc.contributor.author Singh, Shashi Prakash
dc.date.accessioned 2024-07-30T09:58:25Z
dc.date.available 2024-07-30T09:58:25Z
dc.date.issued 2020-12
dc.identifier.uri https://www.tandfonline.com/doi/full/10.1080/19420889.2020.1855854
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15023
dc.description.abstract The Scar/WAVE complex catalyzes the protrusion of pseudopods and lamellipods, and is therefore a principal regulator of cell migration. However, it is unclear how its activity is regulated, beyond a dependence on Rac. Phosphorylation of the proline-rich region, by kinases such as Erk2, has been suggested as an upstream activator. We have recently reported that phosphorylation is not required for complex activation. Rather, it occurs after Scar/WAVE has been activated, and acts as a modulator. Neither chemoattractant signaling nor Erk2 affects the amount of phosphorylation, though in Dictyostelium it is promoted by cell-substrate adhesion. We now report that cell-substrate adhesion also promotes Scar/WAVE2 phosphorylation in mammalian cells, suggesting that the process is evolutionarily conserved. en_US
dc.language.iso en en_US
dc.publisher Taylor & Francis en_US
dc.subject Biology en_US
dc.subject Scar/WAVE en_US
dc.subject Phosphorylation en_US
dc.subject Cell migration en_US
dc.subject Adhesion en_US
dc.title Adhesion stimulates Scar/WAVE phosphorylation in mammalian cells en_US
dc.type Article en_US


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