Regulation of Macropinocytosis by Diacylglycerol Kinase ζ.
Macropinosomes 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 Rh...
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doaj-ff8d2f4db23a4db68df91d15467f85732020-11-25T00:05:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011012e014494210.1371/journal.pone.0144942Regulation of Macropinocytosis by Diacylglycerol Kinase ζ.Ryan ArdKirk MulatzJulia L PomoranskyRobin J ParksLaura Trinkle-MulcahyJohn C BellStephen H GeeMacropinosomes 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.http://europepmc.org/articles/PMC4689489?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ryan Ard Kirk Mulatz Julia L Pomoransky Robin J Parks Laura Trinkle-Mulcahy John C Bell Stephen H Gee |
spellingShingle |
Ryan Ard Kirk Mulatz Julia L Pomoransky Robin J Parks Laura Trinkle-Mulcahy John C Bell Stephen H Gee Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. PLoS ONE |
author_facet |
Ryan Ard Kirk Mulatz Julia L Pomoransky Robin J Parks Laura Trinkle-Mulcahy John C Bell Stephen H Gee |
author_sort |
Ryan Ard |
title |
Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. |
title_short |
Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. |
title_full |
Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. |
title_fullStr |
Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. |
title_full_unstemmed |
Regulation of Macropinocytosis by Diacylglycerol Kinase ζ. |
title_sort |
regulation of macropinocytosis by diacylglycerol kinase ζ. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2015-01-01 |
description |
Macropinosomes 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. |
url |
http://europepmc.org/articles/PMC4689489?pdf=render |
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