Rab11 activity and PtdIns(3)P turnover removes recycling cargo from endosomes

Directional transport of recycling cargo from early endosomes (EE) to the endocytic recycling compartment (ERC) relies on phosphatidylinositol 3-phosphate (PtdIns(3) P ) hydrolysis and activation of the small GTPase Rab11. However, how these events are coordinated is yet unclear. By using a novel ge...

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Veröffentlicht in:Nature chemical biology 2018-08, Vol.14 (8), p.801-810
Hauptverfasser: Campa, Carlo Cosimo, Margaria, Jean Piero, Derle, Abhishek, Del Giudice, Marco, De Santis, Maria Chiara, Gozzelino, Luca, Copperi, Francesca, Bosia, Carla, Hirsch, Emilio
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Sprache:eng
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Zusammenfassung:Directional transport of recycling cargo from early endosomes (EE) to the endocytic recycling compartment (ERC) relies on phosphatidylinositol 3-phosphate (PtdIns(3) P ) hydrolysis and activation of the small GTPase Rab11. However, how these events are coordinated is yet unclear. By using a novel genetically-encoded FRET biosensor for Rab11, we report that generation of endosomal PtdIns(3) P by the clathrin-binding phosphoinositide 3-kinase class 2 alpha (PI3K-C2α) controls the activation of Rab11. Active Rab11, in turn, prompts the recruitment of the phosphatidylinositol 3-phosphatase myotubularin 1 (MTM1), eventually enabling the release of recycling cargo from the EE and its delivery toward the ERC. Our findings thus define that delivery of recycling cargo toward the ERC requires spatial and sequential coupling of Rab11 activity with PtdIns(3) P turnover. A Rab11 FRET biosensor reveals a spatiotemporal interplay between Rab11 and PtdIns(3) P turnover during the removal of recycling cargo from the endosome.
ISSN:1552-4450
1552-4469
DOI:10.1038/s41589-018-0086-4