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TAT-5 and TAT-6 P4-family ATPases regulate the release of extracellular vesicles containing polycystins from Caenorhabditis elegans sensilla
Umeå University, Faculty of Medicine, Umeå Centre for Molecular Medicine (UCMM).
Umeå University, Faculty of Medicine, Umeå Centre for Molecular Medicine (UCMM).
Umeå University, Faculty of Medicine, Department of Integrative Medical Biology (IMB).
Umeå University, Faculty of Medicine, Department of Integrative Medical Biology (IMB).
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(English)Manuscript (preprint) (Other academic)
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:umu:diva-191141OAI: oai:DiVA.org:umu-191141DiVA, id: diva2:1625983
Available from: 2022-01-10 Created: 2022-01-10 Last updated: 2025-03-03
In thesis
1. Studies on lipid transport and extracellular vesicle production in Caenorhabditis elegans ciliated neurons
Open this publication in new window or tab >>Studies on lipid transport and extracellular vesicle production in Caenorhabditis elegans ciliated neurons
2022 (English)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[sv]
Studier om lipidtransport och extracellulära vesiklars produktion i C. elegans cilierade nervceller
Abstract [en]

The cilium is a protrusion of cell membrane. Both the protein and lipid contents of cilia are different from those of other parts of the cell membrane. While the transport of proteins into and out of cilia has been intensively studied, much less is known about how the lipid content of ciliary membranes is regulated. TAT-6 is a P4-family ATPase that is expressed in C. elegans ciliated neurons whose endings are exposed to the environment. To study the function of TAT-6 and that other translocases in lipid transport in C. elegans ciliated neurons, I developed a technique to allow labelling of cilia with lipids. For the first time I used fusogenic liposomes to study the roles of all the TAT proteins in this organism in maintaining the lipid asymmetry in this organelle. Assessment the cilia with these liposomes showed that TAT-5 and TAT-1 translocase activities promote the transport of phosphatidylethanolamine (PE) and phosphatidylserine (PS) respectively and TAT-6 has an overlapping function in transporting both phospholipds. In C. elegans males, certain ciliated neurons release extracellular vesicles (EVs). The cilium is a site of EV biogenesis and shedding. I found that ciliated neurons in tat-6 mutant males produced significantly fewer EVs than those in wild type. tat-1, tat-5 and pad-1 mutants, however, produced far more EVs than those in wild type. PPK-3, CUP-5 and LMP-1 are proteins necessary for endolysosomal trafficking and lysosomes biogenesis, a process in which TAT-1 has previously been shown to function in C. elegans intestinal cells. I found that, like tat-1 mutants, ppk-3, lmp-1 and cup-5 mutant males release significantly greater numbers of EVs from cilia compared with wild-type. I found that increasing and decreasing the cGMP signaling cause defects in the response and turning behavior in male C. elegans respectively. Exposing wild-type males to high levels of 8-Bromoguanosine 3′,5′-cyclic monophosphate strongly reduced response behavior. Males mutant for odr-3, which encodes a G protein were defective in response. Overall my investigations indicate that the regulation of lipid asymmetry and phospholipid transport is required for proper cilia function in C. elegans, that intercellular trafficking and lipid composition have important roles in EVs biogenesis, and that different TAT proteins can affect the size and number of EVs produced. I also showed that in male animals, cGMP is one of the mediators in mating transduction signal and that a high level of cGMP inhibits mating response behavior in male C. elegans. 

Place, publisher, year, edition, pages
Umeå: Umeå University, 2022. p. 70
Series
Umeå University medical dissertations, ISSN 0346-6612
Keywords
C. elegans, cilia, extracellular vesicles, tat, phospholipid translocase, P4-family ATPase
National Category
Cell Biology
Identifiers
urn:nbn:se:umu:diva-191161 (URN)978-91-7855-720-2 (ISBN)978-91-7855-721-9 (ISBN)
Public defence
2022-02-09, Aula Anatomica, Biologihuset, Umeå, 09:00 (English)
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Available from: 2022-01-19 Created: 2022-01-10 Last updated: 2022-01-11Bibliographically approved

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Nilsson, LarsRahmani, ShapourHubert, MadlenWilliams, ChloeGilthorpe, Jonathan D.Lundmark, RichardTuck, Simon

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Umeå Centre for Molecular Medicine (UCMM)Department of Integrative Medical Biology (IMB)Molecular Infection Medicine Sweden (MIMS)
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