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  • Funded Activity

    Chemokine Receptors And Their Role In The Recruitment Of Leucocytes To The Gut

    Funder
    National Health and Medical Research Council
    Funding Amount
    $100,109.00
    More information
    Funded Activity

    Cyclooxygenase Isotypes: Distinct Roles Of COX-1 And COX-2 In Inflammatory Mediator Production

    Funder
    National Health and Medical Research Council
    Funding Amount
    $201,767.00
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    Funded Activity

    Therapy And Mediators Of Human Ocular Inflammation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $220,871.00
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    Funded Activity

    Viscerosensory Neuroimmune Interactions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $336,667.00
    More information
    Funded Activity

    Molecular Interactions Of The Tetraspanins CD37, TSSC6 And CD151 In T Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $566,575.00
    Summary
    The tetraspanins are a new type of protein that are found at the surface of cells. Cells of the immune system, such as white blood cells, display at their surface, up to 20 different tetraspanin proteins. However, the precise contributions of these tetraspanin proteins to immunity is still not clear, nor is it clear exactly how tetraspanin proteins differ from one another and why white blood cells need to display so many different tetraspanins. Using genetic technology we have created mice which .... The tetraspanins are a new type of protein that are found at the surface of cells. Cells of the immune system, such as white blood cells, display at their surface, up to 20 different tetraspanin proteins. However, the precise contributions of these tetraspanin proteins to immunity is still not clear, nor is it clear exactly how tetraspanin proteins differ from one another and why white blood cells need to display so many different tetraspanins. Using genetic technology we have created mice which are unable to express certain individual tetraspanin proteins at their cell surface. Excitingly, the immune systems of these mice are not normal, in particular one type of white blood cell, the T cell responds in an exaggerated manner to stimulation. These results suggest a role for tetraspanins in the control and regulation of the immune system. This project will extend these results and work out the precise molecular mechanism by which the tetraspanins exert this control. In the future, a full understanding of how tetraspanins control T cells may ultimately lead to novel ways of controlling the immune system.
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    Funded Activity

    Uncoupled Research Fellowship

    Funder
    National Health and Medical Research Council
    Funding Amount
    $279,879.00
    Summary
    I am a cell biologist investigating the means by which intracellular compartmentalization of signalling proteins determines signalling outcomes and cell fate. I focus particularly on signals that regulate immune function and cancer progression.
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    Funded Activity

    Differentially Expressed Dendritic Cell Surface Molecules

    Funder
    National Health and Medical Research Council
    Funding Amount
    $482,640.00
    Summary
    Dendritic cells are a very rare type of white blood cell which play a critical role in the initiation of the immune response. They are of particular interest to scientists interested in vaccination, as for a vaccine to work effectively, the vaccine must be presented to the rest of the immune system by the dendritic cell. It has only recently become apparent that there are several types of dendritic cell, and these different types of dendritic cell vary in their ability to present a vaccine to th .... Dendritic cells are a very rare type of white blood cell which play a critical role in the initiation of the immune response. They are of particular interest to scientists interested in vaccination, as for a vaccine to work effectively, the vaccine must be presented to the rest of the immune system by the dendritic cell. It has only recently become apparent that there are several types of dendritic cell, and these different types of dendritic cell vary in their ability to present a vaccine to the immune system. We have already identified some proteins that are expressed on the surface of only one type of dendritic cell. We will explore the possible use of these proteins as a means of delivering a vaccine to only one type of dendritic cell. This project will also identify new genes that are expressed in some types of dendritic cells but not others. These new genes whose expression does differ amongst the dendritic cells are potential targets for manipulating the immune system and ensuring more efficient vaccination.
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    Funded Activity

    Role Of Tetraspanins In Integrin Function And Leukocyte Migration

    Funder
    National Health and Medical Research Council
    Funding Amount
    $419,223.00
    Summary
    Cell migration is a very important component of the immune system. White blood cells, migrate from tissues to lymph nodes to initiate immune responses, and can migrate from blood to sites of inflammation to fight infection. This grant studies a type of protein called a tetraspanin that we believe controls white blood cell migration. Understanding the precise role of tetraspanins in this process will further our understanding of inflammation in disease processes.
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    Funded Activity

    Factors Controlling Leucocyte Migration In Healthy Intestine And In Inflammatory Bowel Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $195,217.00
    Summary
    Inflammatory bowel diseases (IBD) are relapsing and remitting disorders of the intestine that create substantial disability in a relatively young population of patients. Our treatments for these conditions have changed little in the last 30 years and they are commonly accompanied by side effects. Research into the mechanisms controlling the gut inflammation offers promise for the development of novel, targeted and less toxic therapies. The major mediators of damage in IBD are white blood cells r .... Inflammatory bowel diseases (IBD) are relapsing and remitting disorders of the intestine that create substantial disability in a relatively young population of patients. Our treatments for these conditions have changed little in the last 30 years and they are commonly accompanied by side effects. Research into the mechanisms controlling the gut inflammation offers promise for the development of novel, targeted and less toxic therapies. The major mediators of damage in IBD are white blood cells recruited from the circulation to affected intestine. This recruitment is induced by the production in damaged intestine of chemokines, proteins of the immune system that attract and activate white blood cells. Chemokines act through chemokine receptors on the surface of white blood cells, and earlier research by our group has demonstrated that these chemokine receptors can be functionally modulated by neuropeptides, proteins unrelated to chemokines that normally transmit messages within the nervous system. This project aims to explore the chemokines and chemokine receptors responsible for the recruitment of white blood cells to normal and IBD-affected intestine, in order to determine therapeutic targets for novel treatments. Moreover, the role of neuropeptides in modulating the recruitment of white blood cells to the intestine will be examined in cells from the human intestine, both normal and IBD-affected, as well as in an animal model of IBD. This project will provide an understanding of the signals responsible for the attraction of damaging white blood cells to sites of inflammation in the bowel and will indicate mechanisms used by the immune system to regulate those signals. It has the potential to direct us to new therapies that use highly targeted and physiologically appropriate approaches to controlling white blood cell trafficking in health and disease.
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    Funded Activity

    Gene Regulation, Cytokine Regulation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $820,332.00
    Summary
    I am a physician-scientist investigating cellular mechanism of inflammatory injury in animal models of human diseases.
    More information

    Showing 1-10 of 16 Funded Activites

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