SNX27 mediates retromer tubule entry and endosome-to-plasma membrane trafficking of signalling receptors.

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Citation

Temkin P, Lauffer B, Jager S, Cimermancic P, Krogan NJ, von Zastrow M

SNX27 mediates retromer tubule entry and endosome-to-plasma membrane trafficking of signalling receptors.

Nat Cell Biol. 2011 Jun;13(6):715-21. doi: 10.1038/ncb2252. Epub 2011 May 22.

PubMed ID
21602791 [ View in PubMed
]
Abstract

Endocytic sorting of signalling receptors between recycling and degradative pathways is a key cellular process controlling the surface complement of receptors and, accordingly, the cell's ability to respond to specific extracellular stimuli. The beta2 adrenergic receptor (beta2AR) is a prototypical seven-transmembrane signalling receptor that recycles rapidly and efficiently to the plasma membrane after ligand-induced endocytosis. beta2AR recycling is dependent on the receptor's carboxy-terminal PDZ ligand and Rab4. This active sorting process is required for functional resensitization of beta2AR-mediated signalling. Here we show that sequence-directed sorting occurs at the level of entry into retromer tubules and that retromer tubules are associated with Rab4. Furthermore, we show that sorting nexin 27 (SNX27) serves as an essential adaptor protein linking beta2ARs to the retromer tubule. SNX27 does not seem to directly interact with the retromer core complex, but does interact with the retromer-associated Wiskott-Aldrich syndrome protein and SCAR homologue (WASH) complex. The present results identify a role for retromer in endocytic trafficking of signalling receptors, in regulating a receptor-linked signalling pathway, and in mediating direct endosome-to-plasma membrane traffic.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Beta-2 adrenergic receptorP07550Details