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    A Molecular Probe for the Detection of Polar Lipids in Live Cells.

    242354_242354.PDF (14.94Mb)
    Access Status
    Open access
    Authors
    Bader, C.
    Shandala, T.
    Carter, E.
    Ivask, A.
    Guinan, T.
    Hickey, S.
    Werrett, M.
    Wright, Phillip
    Simpson, Peter
    Stagni, S.
    Voelcker, N.
    Lay, P.
    Massi, Massimiliano
    Plush, S.
    Brooks, D.
    Date
    2016
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Bader, C. and Shandala, T. and Carter, E. and Ivask, A. and Guinan, T. and Hickey, S. and Werrett, M. et al. 2016. A Molecular Probe for the Detection of Polar Lipids in Live Cells. PLoS One. 11 (8): e0161557.
    Source Title
    PLoS One
    DOI
    10.1371/journal.pone.0161557
    School
    Nanochemistry Research Institute
    Funding and Sponsorship
    http://purl.org/au-research/grants/arc/FT1301000033
    Remarks

    This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by

    URI
    http://hdl.handle.net/20.500.11937/36711
    Collection
    • Curtin Research Publications
    Abstract

    Lipids have an important role in many aspects of cell biology, including membrane architecture/compartment formation, intracellular traffic, signalling, hormone regulation, inflammation, energy storage and metabolism. Lipid biology is therefore integrally involved in major human diseases, including metabolic disorders, neurodegenerative diseases, obesity, heart disease, immune disorders and cancers, which commonly display altered lipid transport and metabolism. However, the investigation of these important cellular processes has been limited by the availability of specific tools to visualise lipids in live cells. Here we describe the potential for ReZolve-L1™ to localise to intracellular compartments containing polar lipids, such as for example sphingomyelin and phosphatidylethanolamine. In live Drosophila fat body tissue from third instar larvae, ReZolve-L1™ interacted mainly with lipid droplets, including the core region of these organelles. The presence of polar lipids in the core of these lipid droplets was confirmed by Raman mapping and while this was consistent with the distribution of ReZolve-L1™ it did not exclude that the molecular probe might be detecting other lipid species. In response to complete starvation conditions, ReZolve-L1™ was detected mainly in Atg8-GFP autophagic compartments, and showed reduced staining in the lipid droplets of fat body cells. The induction of autophagy by Tor inhibition also increased ReZolve-L1™ detection in autophagic compartments, whereas Atg9 knock down impaired autophagosome formation and altered the distribution of ReZolve-L1™. Finally, during Drosophila metamorphosis fat body tissues showed increased ReZolve-L1™ staining in autophagic compartments at two hours post puparium formation, when compared to earlier developmental time points. We concluded that ReZolve-L1™ is a new live cell imaging tool, which can be used as an imaging reagent for the detection of polar lipids in different intracellular compartments.

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