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Field of Research : Signal transduction
Research Topic : SIGNAL
Australian State/Territory : NSW
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Biochemistry and cell biology (3)
Signal transduction (3)
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  • Active Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE240101055

    Funder
    Australian Research Council
    Funding Amount
    $448,737.00
    Summary
    How blood vessel stiffness regulates their growth and maintenance. This project aims to reveal an unidentified molecular mechanism of how endothelial cells in the walls of blood vessels detect stiffness of the surrounding environment in order to regulate blood vessel growth and maintenance. The results are expected to advance the emerging field of mechanobiology by combining cutting-edge cell biology and microscopy techniques carried out in novel 3D cell culture and unique quail models. The bene .... How blood vessel stiffness regulates their growth and maintenance. This project aims to reveal an unidentified molecular mechanism of how endothelial cells in the walls of blood vessels detect stiffness of the surrounding environment in order to regulate blood vessel growth and maintenance. The results are expected to advance the emerging field of mechanobiology by combining cutting-edge cell biology and microscopy techniques carried out in novel 3D cell culture and unique quail models. The benefits of these outcomes include generation of knowledge on the impact of tissue stiffness on the signalling mechanisms that drive formation and maintenance of blood vessels. In the long term, this fundamental understanding could give rise to major developments in emerging industries such as organ bioengineering.
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    Active Funded Activity

    ARC Future Fellowships - Grant ID: FT220100159

    Funder
    Australian Research Council
    Funding Amount
    $832,068.00
    Summary
    Sensing biomechanical forces in the heart. Mechanosensitive ion channels are key molecules that define how each heart cell interacts with their physical environment. Yet how they enable cells to decode biomechanical cues remains poorly understood. At the heart of this problem is a lack of tools to quantify the force required for activation. This project aims to develop novel technologies to record the activity of these essential channels in a critical cell type within the heart, and use this inf .... Sensing biomechanical forces in the heart. Mechanosensitive ion channels are key molecules that define how each heart cell interacts with their physical environment. Yet how they enable cells to decode biomechanical cues remains poorly understood. At the heart of this problem is a lack of tools to quantify the force required for activation. This project aims to develop novel technologies to record the activity of these essential channels in a critical cell type within the heart, and use this information in addition to micro-engineering approaches to fully understand the role of these channels in force sensing and generation, at both the single cell and micro-tissue levels. This knowledge and technology has broad utility that extends far beyond cardiac biology into multiple fields.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP240101768

    Funder
    Australian Research Council
    Funding Amount
    $597,127.00
    Summary
    Novel mechano-signalling pathways at sites of cellular adhesion. Piezo channels are membrane proteins that detect mechanical cues and underlie our sense of touch. We aim to characterize the first protein regulator of Piezo channels by developing and utilizing novel technologies including acoustic forces to monitor Piezo channel function. The significance of this study is underscored by the wide spread expression of Piezo channels and their involvement in many cellular processes. Expected outcome .... Novel mechano-signalling pathways at sites of cellular adhesion. Piezo channels are membrane proteins that detect mechanical cues and underlie our sense of touch. We aim to characterize the first protein regulator of Piezo channels by developing and utilizing novel technologies including acoustic forces to monitor Piezo channel function. The significance of this study is underscored by the wide spread expression of Piezo channels and their involvement in many cellular processes. Expected outcomes are novel technologies to study mechanobiology, patentable peptide-based Piezo modulators and a new conceptual paradigm for understanding cellular mechanosensing. This knowledge will benefit a broad scientific community through technological advancements and pharmacological agents to manipulate Piezo channels.
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