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Regulation of Macropinocytosis by Diacylglycerol Kinase ζ

dc.contributor.authorArd, Ryan
dc.contributor.authorMulatz, Kirk
dc.contributor.authorPomoransky, Julia L.
dc.contributor.authorParks, Robin J.
dc.contributor.authorTrinkle-Mulcahy, Laura
dc.contributor.authorBell, John C.
dc.contributor.authorGee, Stephen H.
dc.date.accessioned2016-04-16T19:05:08Z
dc.date.available2016-04-16T19:05:08Z
dc.date.issued2015
dc.description.abstractMacropinosomes arise from the closure of plasma membrane ruffles to bring about the non-selective uptake of nutrients and solutes into cells. The morphological changes underlying ruffle formation and macropinosome biogenesis are driven by actin cytoskeleton rearrangements under the control of the Rho GTPase Rac1. We showed previously that Rac1 is activated by diacylglycerol kinase ζ (DGKζ), which phosphorylates diacylglycerol to yield phosphatidic acid. Here, we show DGKζ is required for optimal macropinocytosis induced by growth factor stimulation of mouse embryonic fibroblasts. Time-lapse imaging of live cells and quantitative analysis revealed DGKζ was associated with membrane ruffles and nascent macropinosomes. Macropinocytosis was attenuated in DGKζ-null cells, as determined by live imaging and vaccinia virus uptake experiments. Moreover, macropinosomes that did form in DGKζ-null cells were smaller than those found in wild type cells. Rescue of this defect required DGKζ catalytic activity, consistent with it also being required for Rac1 activation. A constitutively membrane bound DGKζ mutant substantially increased the size of macropinosomes and potentiated the effect of a constitutively active Rac1 mutant on macropinocytosis. Collectively, our results suggest DGKζ functions in concert with Rac1 to regulate macropinocytosis.en
dc.identifier.citationPLOS ONE 10(12)en
dc.identifier.doi10.1371/journal.pone.0144942en
dc.identifier.issn1932-6203en
dc.identifier.urihttp://hdl.handle.net/10393/34510
dc.language.isoenen
dc.titleRegulation of Macropinocytosis by Diacylglycerol Kinase ζen
dc.typeArticleen

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