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Research Topic : PROTEIN PHOSPHATASE
Scheme : Project Grants
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  • Funded Activities (309)
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  • Funded Activity

    Trafficking Mechanisms Governing Receptor Availability For Signalling

    Funder
    National Health and Medical Research Council
    Funding Amount
    $526,978.00
    Summary
    Receptors on the cell surface allow cells to respond to their environment. We have recently discovered a new pathway for controlling the amount of receptors displayed on the cell surface, errors within which will lead to defects in development and diseases like cancer. We are studying how this new pathway controls the balance between how much receptors are destroyed after being activated and how much are recycled back for re-use.
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    Funded Activity

    PTPs In The CNS Control Of WAT Browning

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,168,325.00
    Summary
    Obesity is caused by an energy imbalance, where energy intake from eating food exceeds energy expended by physical exertion and metabolism. This proposal will provide a fundamental advance in our understanding of how the brain communicates with fat to control energy expenditure and body weight.
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    Funded Activity

    Protein Phosphatase 2A Methylation: Regulation And Functional Significance For Tauopathies

    Funder
    National Health and Medical Research Council
    Funding Amount
    $470,713.00
    Summary
    Clinical studies have revealed that low blood levels of the vitamin folate are a risk factor for cognitive impairment, depression and dementia, which are prevalent in the elderly. Deregulation of the protein tau is a key event in Alzheimer’s disease pathogenesis. This project will utilize cell culture and aged mouse models to determine how alterations in folate status and deregulation of protein phosphatase 2A affect the regulation of tau and other key brain processes that become altered in Alzh .... Clinical studies have revealed that low blood levels of the vitamin folate are a risk factor for cognitive impairment, depression and dementia, which are prevalent in the elderly. Deregulation of the protein tau is a key event in Alzheimer’s disease pathogenesis. This project will utilize cell culture and aged mouse models to determine how alterations in folate status and deregulation of protein phosphatase 2A affect the regulation of tau and other key brain processes that become altered in Alzheimer’s disease.
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    Funded Activity

    Hepatic Oxidative Stress, PTPs & STAT Signalling In Obesity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,086,547.00
    Summary
    Obesity is increasing at an alarming rate worldwide and is a leading cause of morbidity and mortality. Obesity is causally linked to the development of insulin resistance, a prelude to type 2 diabetes. In this proposal we will define a novel liver centric mechanism by which insulin resistance and oxidative stress may promote the development of morbid obesity, type 2 diabetes and liver disease.
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    Funded Activity

    Characterisation Of A Feedback Loop In T Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $605,251.00
    Summary
    T cells play a central role in the immune response. The primary event in T cell activation is the triggering of a specific T cell receptor (TCR). Our studies will define new mechanisms for the regulation of TCR-mediated T cell responses. Our studies may yield novel insight into processes that contribute to the development of type 1 diabetes & inflammatory bowel disease.
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    Funded Activity

    Regulation Of Hypothalamic Insulin & Leptin Signalling By TCPTP

    Funder
    National Health and Medical Research Council
    Funding Amount
    $758,504.00
    Summary
    Insulin & leptin signal in the brain to lower blood glucose, suppress food intake, increase activity & increase energy expenditure. Obesity diminishes the abilities of insulin & leptin to signal. This proposal will determine if the enzyme TCPTP terminates insulin & leptin signaling in the brain. Our studies will provide insight into the molecular causes of obesity & may identify a novel therapeutic target for the treatment of obesity & type 2 diabetes.
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    Funded Activity

    The Role Of TCPTP In Liver Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $781,301.00
    Summary
    There are ~1.6 billion overweight adults worldwide & this is predicted to rise to 2.3 billion by 2015. In Australia > 2/3 of adults are overweight or obese. Obesity is a key factor in the progression of many human malignancies. Obesity poses the greatest risk for the development hepatocellular carcinoma (HCC), a deadly cancer refractory to nearly all available anti-cancer therapies. This application will delineate the molecular mechanisms by which obesity promotes HCC development.
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    Funded Activity

    The Role Of The T Cell Protein Tyrosine Phosphatase In Autoimmunity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $654,725.00
    Summary
    Autoimmune diseases such as type 1 diabetes, Crohns disease & rheumatoid arthritis collectively affect ~5% of Australians & are associated with the immune system attacking the body’s organs as if they were a foreign infection. Genetic studies in humans & animal studies point towards the enzyme TCPTP being important in the prevention of autoimmunity. This proposal will define the molecular & cellular pathways by which TCPTP prevents autoimmunity.
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    Funded Activity

    Phosphatase Regulators Mediate Long-term Changes In Presynaptic Terminals

    Funder
    National Health and Medical Research Council
    Funding Amount
    $984,163.00
    Summary
    The strength of communication between each nerve cell in the brain depends on how active that nerve cell has been. This enables the brain to be adaptable and is a way for the brain to set up circuits that underlie how we learn and remember. More or less release of chemical messengers (neurotransmitters) into nerve cell junctions changes the strength of nerve cell communication. We have discovered a new chemical signalling pathway controlling neurotransmitter release.
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    Funded Activity

    Cardiovascular Effects Of Enhanced Leptin Signalling

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,200,972.00
    Summary
    Leptin treatment causes weight loss, but leptin also increases blood pressure. We wish to determine if increasing leptin signalling, by modifying signal transduction pathways within leptin sensitive cells in the brain, can reduce weight without increasing blood pressure.
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    Showing 1-10 of 309 Funded Activites

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