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Field of Research : Cellular interactions (incl. adhesion matrix cell wall)
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Cellular interactions (incl. adhesion matrix cell wall) (8)
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  • Researchers (28)
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  • Active Funded Activity

    Australian Laureate Fellowships - Grant ID: FL230100100

    Funder
    Australian Research Council
    Funding Amount
    $3,300,000.00
    Summary
    Forces in Nature: Tissue mechanics and cell sociology. Epithelial cells cover surfaces in the body, forming a shield to protect us from the environment. Despite their importance, we understand poorly how the cells communicate. This project aims to test the novel concept that epithelial cells communicate via transmission and detection of mechanical forces, using an innovative combination of cellular and biophysical experiments and physical theory. The expected outcomes are new knowledge, interdis .... Forces in Nature: Tissue mechanics and cell sociology. Epithelial cells cover surfaces in the body, forming a shield to protect us from the environment. Despite their importance, we understand poorly how the cells communicate. This project aims to test the novel concept that epithelial cells communicate via transmission and detection of mechanical forces, using an innovative combination of cellular and biophysical experiments and physical theory. The expected outcomes are new knowledge, interdisciplinary training for young scientists, new national research capacity and growing international collaborations. Benefits include enhancing Australia’s scientific linkages and research capacity and providing fundamental knowledge that could lead to future advances in bioengineering and drug discovery.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230100504

    Funder
    Australian Research Council
    Funding Amount
    $640,000.00
    Summary
    Migration-Dependent Signalling in Macrophages . The project aims to investigate a mechanism of communication used by immune cells to guide each other towards sites of damage. The project will characterise newly revealed cell signalling membrane trails left behind by migrating cells, utilising biochemistry, innovative imaging and microscopy and a transparent zebrafish model to view cell migration through living tissues. Expected outcomes include new fundamental knowledge in the area of immune cel .... Migration-Dependent Signalling in Macrophages . The project aims to investigate a mechanism of communication used by immune cells to guide each other towards sites of damage. The project will characterise newly revealed cell signalling membrane trails left behind by migrating cells, utilising biochemistry, innovative imaging and microscopy and a transparent zebrafish model to view cell migration through living tissues. Expected outcomes include new fundamental knowledge in the area of immune cell migration with relevance to the basic biology of inflammation, repair and regeneration and new innovations for cell imaging. Significant benefits are expected to arise from this new knowledge and from advanced skills training and improved national capabilities in bio-imaging and analysis.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230100135

    Funder
    Australian Research Council
    Funding Amount
    $599,000.00
    Summary
    Identifying how cortical bone microstructure deteriorates with age. This project aims to define the disruptions responsible for the gradual weakening of the skeleton in ageing by integrating a range of high-resolution imaging, biomechanical, and computational methods. The expected significance of this project includes a full definition and comparison of the cellular and subcellular organisation of bone from young and elderly individuals. Expected outcomes of this international project include th .... Identifying how cortical bone microstructure deteriorates with age. This project aims to define the disruptions responsible for the gradual weakening of the skeleton in ageing by integrating a range of high-resolution imaging, biomechanical, and computational methods. The expected significance of this project includes a full definition and comparison of the cellular and subcellular organisation of bone from young and elderly individuals. Expected outcomes of this international project include the establishment of a new multidisciplinary research team, and the development of a new data-driven theoretical framework for understanding the nature and the causes of age-related bone fragility. Potential long-term benefits include new ways to treat age-related osteoporosis.
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    Active Funded Activity

    Bioprinting And Advanced Visualisation Of Novel 3D Model Systems.

    Funder
    Australian Research Council
    Funding Amount
    $1,009,078.00
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230102269

    Funder
    Australian Research Council
    Funding Amount
    $459,000.00
    Summary
    Click chemistry to reveal how neurons and glia shape perineuronal nets . The extracellular matrix (ECM) and its perineuronal nets (which are net-like structures with holes wrapped around neurons) are largely underexplored, despite representing a remarkable 20% of the brain’s total volume and having been suggested to be involved in many brain functions. Interestingly, digestion of the ECM improves learning and memory, but deficits return once the ECM has reformed. However, how this ECM remodellin .... Click chemistry to reveal how neurons and glia shape perineuronal nets . The extracellular matrix (ECM) and its perineuronal nets (which are net-like structures with holes wrapped around neurons) are largely underexplored, despite representing a remarkable 20% of the brain’s total volume and having been suggested to be involved in many brain functions. Interestingly, digestion of the ECM improves learning and memory, but deficits return once the ECM has reformed. However, how this ECM remodelling is organised at a cell-type level is not understood. Here we aim to close this knowledge gap, using cutting-edge technology including bioconjugation and ultrasound-mediated cargo delivery. Together, this project aims to contribute to a deeper understanding of this major brain compartment in neuronal function.
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    Active Funded Activity

    ARC Future Fellowships - Grant ID: FT220100092

    Funder
    Australian Research Council
    Funding Amount
    $1,071,010.00
    Summary
    Engineering nanomaterial interactions with the cell surface. This Fellowship aims to advance understanding of the endothelial cell surface, a key tissue barrier, and its interactions with nanomaterials. Enabled by cross-disciplinary collaboration, it expects to develop knowledge in matrix biology of the cell surface and materials as well as new methods to analyse their interactions. This is expected to unravel causal relationships between nanomaterial features and interactions at the cell surfac .... Engineering nanomaterial interactions with the cell surface. This Fellowship aims to advance understanding of the endothelial cell surface, a key tissue barrier, and its interactions with nanomaterials. Enabled by cross-disciplinary collaboration, it expects to develop knowledge in matrix biology of the cell surface and materials as well as new methods to analyse their interactions. This is expected to unravel causal relationships between nanomaterial features and interactions at the cell surface which will be integrated to engineer optimised materials. This will address the current and critical challenges of nanomaterial technologies in the efficient and targeted interactions with cells with long-term benefits for the consumer, biotechnology and healthcare sectors.
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    Active Funded Activity

    ARC Future Fellowships - Grant ID: FT230100249

    Funder
    Australian Research Council
    Funding Amount
    $970,566.00
    Summary
    Programming physical and biological cues to promote vessel growth . This project aims to engineer new hydrogel-based biomaterials that allow spatio-temporal modulation of physical and biological cues to direct blood vessels growth, as well as compatible with advanced bioprinting platforms. It will generate new knowledge in biomaterials, biofabrication and advanced material processing. Expected outcomes include new knowledge in biomaterial-vascular interaction, novel vascular bioinks, cross-disci .... Programming physical and biological cues to promote vessel growth . This project aims to engineer new hydrogel-based biomaterials that allow spatio-temporal modulation of physical and biological cues to direct blood vessels growth, as well as compatible with advanced bioprinting platforms. It will generate new knowledge in biomaterials, biofabrication and advanced material processing. Expected outcomes include new knowledge in biomaterial-vascular interaction, novel vascular bioinks, cross-disciplinary, international collaboration and research training. This project will provide significant benefit to Australia's scholarly output and reputation, as well as long term benefits to biomedical, veterinary and cosmetic through new materials and cutting-edge manufacturing platforms.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230100393

    Funder
    Australian Research Council
    Funding Amount
    $673,490.00
    Summary
    Adrenomedullin: a specific regulator of venous vessel integrity. Arteries and veins display different adhesive properties, which enable them to fulfil their physiological roles. We are yet to understand the mechanisms that establish and maintain adhesive function in different vessel types. We have discovered that signalling by the peptide Adrenomedullin (ADM) is a key mediator of adhesion, only in veins but not arteries. This project aims to utilise innovative models (zebrafish, mouse and bioeng .... Adrenomedullin: a specific regulator of venous vessel integrity. Arteries and veins display different adhesive properties, which enable them to fulfil their physiological roles. We are yet to understand the mechanisms that establish and maintain adhesive function in different vessel types. We have discovered that signalling by the peptide Adrenomedullin (ADM) is a key mediator of adhesion, only in veins but not arteries. This project aims to utilise innovative models (zebrafish, mouse and bioengineered vessels) to identify the biochemical and mechanical mechanisms by which ADM controls venous adhesion. Outcomes will improve our understanding on how vessel integrity is controlled across vessel types and will expand the scope of Australian research by informing efforts to vascularise engineered tissues.
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    Showing 1-8 of 8 Funded Activites

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