Our long-term goal in this proposal is to identify and understand the cellular components that transport internalized endocytic cargo from endosomes to the Golgi apparatus (retrograde recycling), and to understand how this process regulates, and is integrated within, intercellular signaling pathways. Retrograde recycling has recently been linked to multiple metazoan-specific processes such as the generation of Wnt signaling gradients, AMPA-receptor signaling in the nervous system, clearance of dead apoptotic cells, and regulation of epithelial polarity. Wnt signaling requires endosome-to-Golgi retrieval of the Wnt ligand chaperone MIG-14/Wntless, and the molecular details of MIG-14/Wntless recycling have proven to be highly conserved in C. elegans, Drosophila, and mammalian cells. Without retrograde recycling, transmembrane cargo proteins such as MIG-14/Wntless aberrantly enter the lysosome and are degraded, thus depleting the functional pool of such proteins from the cell. To gain novel insight into how retrograde recycling functions, and how it influences intercellular signaling mechanisms in multicellular animals, we have pioneered analysis of the polarized intestinal epithelium of C. elegans. In novel preliminary work we discovered that TGF?-signaling is impaired in retrograde recycling mutants. We plan to further test the hypothesis that TGF?-receptors are retrograde cargo, and test phylogenetic conservation of this mechanism in Drosophila and mammalian cells. In addition, our team has discovered previously unsuspected requirements for endosome regulatory proteins beyond the well-studied retromer complex. These novel regulators include the J-domain co-chaperone RME-8. We plan to test the hypothesis that RME-8 regulates the disassembly of the endosomal flat clathrin lattice, mediating a feedback loop between retromer and the ESCRT-driven degradation machinery that is present on the same endosomes. In addition we have identified an entire additional protein complex involved in retrograde recycling of MIG-14/Wntless. This protein complex appears to be associated with the recycling endosome, and contains modules for membrane binding, membrane bending, and actin nucleation. We plan to determine how this protein complex influences MIG-14/Wntless recycling, test its ability to influence other retrograde cargo including TGF?-receptors, and test for conservation of function in mammalian cells. We expect that our findings will provide unique insight into how trafficking mechanisms influence signaling pathways, and will improve our ability to treat diverse diseases that arise from misregulation of receptor signaling strength, such as in cancers, and other diseases associated with misregulated retrograde recycling including Alzheimer's and Parkinson's diseases.

Public Health Relevance

This proposal focuses on endosome-to-Golgi transport, a fundamental cellular process that contributes to cellular signaling pathways (Wnt and TGF?) linked to cancer, the degradation of dead cells important for development and immunity, and the proper function of many other key events in human metabolism required for normal health and associated with certain disease states (e.g. lysosomal storage disease - Mannose-6- Phosphate receptors, and Menkes disease - ATP7A copper transporters). Endosome-to- Golgi transport is also required for the pathogenicity of certain toxins, such as Shiga and Ricin. A better understanding of the mechanisms controlling retrograde transport will be profoundly important in identifying therapeutic targets to combat these diseases.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
Research Project (R01)
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Membrane Biology and Protein Processing Study Section (MBPP)
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Ainsztein, Alexandra M
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Rutgers University
Schools of Arts and Sciences
New Brunswick
United States
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Zhang, Junbing; Liu, Jinchao; Norris, Anne et al. (2018) A novel requirement for ubiquitin-conjugating enzyme UBC-13 in retrograde recycling of MIG-14/Wntless and Wnt signaling. Mol Biol Cell 29:2098-2112
Savage-Dunn, Cathy; Padgett, Richard W (2017) The TGF-? Family in Caenorhabditis elegans. Cold Spring Harb Perspect Biol 9:
Norris, Anne; Tammineni, Prasad; Wang, Simon et al. (2017) SNX-1 and RME-8 oppose the assembly of HGRS-1/ESCRT-0 degradative microdomains on endosomes. Proc Natl Acad Sci U S A 114:E307-E316
Gleason, Adenrele M; Nguyen, Ken C Q; Hall, David H et al. (2016) Syndapin/SDPN-1 is required for endocytic recycling and endosomal actin association in the C. elegans intestine. Mol Biol Cell :
Wang, Peixiang; Liu, Hang; Wang, Yu et al. (2016) RAB-10 Promotes EHBP-1 Bridging of Filamentous Actin and Tubular Recycling Endosomes. PLoS Genet 12:e1006093
Akhurst, Rosemary J; Padgett, Richard W (2015) Matters of context guide future research in TGF? superfamily signaling. Sci Signal 8:re10
Bai, Zhiyong; Grant, Barth D (2015) A TOCA/CDC-42/PAR/WAVE functional module required for retrograde endocytic recycling. Proc Natl Acad Sci U S A 112:E1443-52
Sato, Ken; Norris, Anne; Sato, Miyuki et al. (2014) C. elegans as a model for membrane traffic. WormBook :1-47
Gleason, Ryan J; Akintobi, Adenrele M; Grant, Barth D et al. (2014) BMP signaling requires retromer-dependent recycling of the type I receptor. Proc Natl Acad Sci U S A 111:2578-83
Schweinsberg, Peter J; Grant, Barth D (2013) C. elegans gene transformation by microparticle bombardment. WormBook :1-10