SNX5 targets a monoamine transporter to the TGN for assembly into dense core vesicles by AP-3

Author:

Xu Hongfei12ORCID,Chang Fei2,Jain Shweta1,Heller Bradley Austin1,Han Xu2,Liu Yongjian23,Edwards Robert H.1ORCID

Affiliation:

1. Departments of Neurology and Physiology, University of California San Francisco, San Francisco, CA 1

2. Jiangsu Key Laboratory of Xenotransplantation, School of Basic Medical Science, Nanjing Medical University, Nanjing, China 2

3. Departments of Pharmacology and Biological Chemistry, University of Pittsburgh, Pittsburgh, PA 3

Abstract

The time course of signaling by peptide hormones, neural peptides, and other neuromodulators depends on their storage inside dense core vesicles (DCVs). Adaptor protein 3 (AP-3) assembles the membrane proteins that confer regulated release of DCVs and is thought to promote their trafficking from endosomes directly to maturing DCVs. We now find that regulated monoamine release from DCVs requires sorting nexin 5 (SNX5). Loss of SNX5 disrupts trafficking of the vesicular monoamine transporter (VMAT) to DCVs. The mechanism involves a role for SNX5 in retrograde transport of VMAT from endosomes to the TGN. However, this role for SNX5 conflicts with the proposed function of AP-3 in trafficking from endosomes directly to DCVs. We now identify a transient role for AP-3 at the TGN, where it associates with DCV cargo. Thus, retrograde transport from endosomes by SNX5 enables DCV assembly at the TGN by AP-3, resolving the apparent antagonism. A novel role for AP-3 at the TGN has implications for other organelles that also depend on this adaptor.

Funder

National Nature Science Foundation of China

John and Helen Cahill Family Endowed Chair

Publisher

Rockefeller University Press

Subject

Cell Biology

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