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Research Topic : golgi
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  • Funded Activities (17)
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  • Funded Activity

    Organisation And Trafficking Of Golgi Glycosyltransferases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $229,671.00
    More information
    Funded Activity

    Molecular Characterisation Of Caveolae Formation And Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $325,732.00
    More information
    Funded Activity

    Characterisation Of Cellular Signals For Protein Sortin G And Secretion.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $136,415.00
    More information
    Funded Activity

    Membrane Dynamics In Protein Trafficking

    Funder
    National Health and Medical Research Council
    Funding Amount
    $198,440.00
    More information
    Funded Activity

    Cell Cucle Regulation Of The Actin Cytoskeleton

    Funder
    National Health and Medical Research Council
    Funding Amount
    $55,048.00
    More information
    Funded Activity

    Characterisation Of Cellular Signals For Protein Sortin G And Secretion

    Funder
    National Health and Medical Research Council
    Funding Amount
    $203,328.00
    More information
    Funded Activity

    G Proteins Regulate Secretion

    Funder
    National Health and Medical Research Council
    Funding Amount
    $471,577.00
    More information
    Funded Activity

    TNF Traffic And Secretion In Astrocytes And Microglial Cells: Unveilling New Targets For Ischemic Stroke

    Funder
    National Health and Medical Research Council
    Funding Amount
    $585,070.00
    Summary
    Neurodegenerative disorders share a similar pathway to disastrous neurotoxicity, which occurs through the release of cytokines such as tumour necrosis factor-a (TNF) from glial cells. TNF controls inflammation but its excessive secretion in the brain is highly detrimental. The mechanism of TNF secretion is unknown but strategies aimed at reducing it have therapeutic potential. This grant proposes to study TNF discharge to find new ways to reduce secretion and confer protection in a stroke model.
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    Funded Activity

    Regulating The Secretion Of Inflammatory Cytokines

    Funder
    National Health and Medical Research Council
    Funding Amount
    $558,441.00
    Summary
    Cytokines or chemical messengers released by cells are essential for controlling immune responses but, in excess, they cause Crohn's disease and arthritis. Our research aims to block cytokine release as a novel way to ameliorate disease. We have identified specific cellular proteins, called golgins, that can be targeted to reduce cytokines. Here, characterization of golgin mediated cytokine transport in cells and in a mouse disease model is necessary to translate these findings for human benefit
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    Funded Activity

    Cytokine Secretion: A Model For Protein Trafficking.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $204,111.00
    Summary
    TNF-a is an inflammatory cytokine with important roles in host defense, tumour regulation and energy homeostatis, however the oversecretion of TNF-a is also a major cause of septic shock, rheumatoid arthritis, Chron?s disease and the cachexia of cancer. TNF-a synthesis and its release from the surface of cells are relatively well understood. However little is known about its trafficking through the secretory pathway of cells. Understanding this process has the potential to provide new ways of co .... TNF-a is an inflammatory cytokine with important roles in host defense, tumour regulation and energy homeostatis, however the oversecretion of TNF-a is also a major cause of septic shock, rheumatoid arthritis, Chron?s disease and the cachexia of cancer. TNF-a synthesis and its release from the surface of cells are relatively well understood. However little is known about its trafficking through the secretory pathway of cells. Understanding this process has the potential to provide new ways of controlling the secretion of TNF-a. In previous work we have characterized transport vesicles and cytoskeletal proteins involved in secretory pathways of epithelial cells. We now propose to focus on the characterization of transport vesicles, and the roles of actin and myosins involved in TNF-a secretion in macrophages. These studies will rely on introducing new technology to this line of research. Fluorescent tagged constructs of TNF-a will be expressed and viewed in living cells to analyse the secretory pathway and measure the transport of TNF-a from its site of accumulation in the Golgi complex to the cell surface. This work aims to identify membrane-bound vesicles and vesicle-associated proteins that target TNF-a for secretion. We will begin to investigate the role of actin and myosins, using drugs and microinjected peptides to block their function. Overall these studies will provide important cell biological information about protein trafficking in cells. Cytokine secretion is important in immunity and cancer, information important to both fields will be gained from these studies.
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