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First published online 12 January 2009
doi: 10.1242/jcs.037051

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EHD3 regulates early-endosome-to-Golgi transport and preserves Golgi morphology

¹ Department of Biochemistry and Molecular Biology and Eppley Cancer Center, University of Nebraska Medical Center, Omaha, NE 68198, USA
² Department of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA
³ Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA

^* Author for correspondence (e-mail: scaplan{at}unmc.edu)

Accepted 23 October 2008

Depletion of EHD3 affects sorting in endosomes by altering the kinetics and route of receptor recycling to the plasma membrane. Here we demonstrate that siRNA knockdown of EHD3, or its interaction partner rabenosyn-5, causes redistribution of sorting nexin 1 (SNX1) to enlarged early endosomes and disrupts transport of internalized Shiga toxin B subunit (STxB) to the Golgi. Moreover, under these conditions, Golgi morphology appears as a series of highly dispersed and fragmented stacks that maintain characteristics of cis-, medial- and trans-Golgi membranes. Although Arf1 still assembled onto these dispersed Golgi membranes, the level of AP-1 -adaptin recruited to the Golgi was diminished. Whereas VSV-G-secretion from the dispersed Golgi remained largely unaffected, the distribution of mannose 6-phosphate receptor (M6PR) was altered: it remained in peripheral endosomes and did not return to the Golgi. Cathepsin D, a hydrolase that is normally transported to lysosomes via an M6PR-dependent pathway, remained trapped at the Golgi. Our findings support a role for EHD3 in regulating endosome-to-Golgi transport, and as a consequence, lysosomal biosynthetic, but not secretory, transport pathways are also affected. These data also suggest that impaired endosome-to-Golgi transport and the resulting lack of recruitment of AP-1 -adaptin to Golgi membranes affect Golgi morphology.

Key words: EHD3, Early endosome, Golgi, Retrograde transport, Mannose-6-phosphate receptor

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