I am a cell biologist who studies the molecular mechanisms that couple cells together into tissues in the body. These adhesion mechanisms are essential during development, support normal tissue turnover and are disrupted in human disease. My research aims to understand how cell adhesion functions normally and how it is disturbed in inflammation and cancer.
Cytoskeletal Regulation Of Adhesion Structure And Cell Movement
Funder
National Health and Medical Research Council
Funding Amount
$60,420.00
Summary
Metastatic (secondary) cancers are a frequent cause of patient mortality. Central to the development of metastasis is cell motility-movement. A key component of cell movement is the way that cells bind and release the extra-cellular matrix as they move. By understanding how the dynamics of cell interaction with the matrix are regulated, we will identify molecules that are critical to the development of metastatic cancer and thus novel targets for inhibition of metastasis.
Investigation Of A New Leukocyte Recruitment Mechanism At Sites Of Vascular Injury
Funder
National Health and Medical Research Council
Funding Amount
$547,216.00
Summary
Blood clots formed at sites of small vessel injury can cause damage of vital organs by obstructing blood flow and promoting a proinflammatory response by efficiently recruiting and activating leukocytes. The molecular mechanisms responsible for the latter event are poorly defined. We have established a new mouse model, gained novel insights into the leukocyte recruitment by blood clots, and aim to define the precise mechanism for this process in this application.
Mechanobiology Of Epithelial Homeostasis In Health And Disease
Funder
National Health and Medical Research Council
Funding Amount
$876,005.00
Summary
Epithelial tissues, such as the lung, fundamentally protect the body from its external environment. For this, they must detect and respond to danger. My work has discovered a new biological system where cells monitor changes in mechanical forces as a sign of danger. Diseases such as inflammation and cancer occur when this detection system fails. This Fellowship builds on my lab’s pioneering work to understand how force is used to sense danger, and how disease occurs when it goes awry.
UNDERSTANDING FOCAL ADHESION DYNAMICS IN CELL MIGRATION
Funder
National Health and Medical Research Council
Funding Amount
$268,944.00
Summary
Metastatic (secondary) cancers are a frequent cause of patient mortality. Central to the development of metastasis is cell motility-movement. A key component of cell movement is the way that cells bind and release the extra-cellular matrix as they move. By understanding how the dynamics of cell interaction with the matrix are regulated, we will identify molecules that are critical to the development of metastatic cancer and thus novel targets for inhibition of metastasis.
How Caveolae Condition Tissue Mechanics For An Anti-tumor Niche.
Funder
National Health and Medical Research Council
Funding Amount
$1,091,226.00
Summary
The outcome of cancer is determined not only by the behaviour of the cancer cell, but also by how the normal tissue cells of the body respond to it. This project investigates how tissue cells that surround cancer cells can eliminate early cancers from the body. It develops on newly-discovered mechanisms that allow epithelial tissues to detect and physically expel cancer cells. This mechanism can protect us from cancer, but potentially allow cancer to develop when it fails.
Functional Characterisation Of A Maurer's Cleft Protein Involved In Adhesion Of Malaria-infected Red Blood Cells
Funder
National Health and Medical Research Council
Funding Amount
$160,500.00
Summary
Malaria is a serious disease that affects half of the world's population and frequently kills humans after a bout of high fever and coma. Many of those who die are young children who live in areas of the world where health care is very poor. The effectiveness of drugs that we currently have available to prevent or treat malaria is rapidly reducing and there is no vaccine available to prevent people from catching the disease. Our research is important because in order to make better medicines for ....Malaria is a serious disease that affects half of the world's population and frequently kills humans after a bout of high fever and coma. Many of those who die are young children who live in areas of the world where health care is very poor. The effectiveness of drugs that we currently have available to prevent or treat malaria is rapidly reducing and there is no vaccine available to prevent people from catching the disease. Our research is important because in order to make better medicines for malaria we have to get to know more about how the malaria parasite makes people sick. The most vicious form of malaria is caused by a tiny parasite called Plasmodium falciparum that lives inside the red blood cells in our bodies. As these minute parasites grow, they make a lot of major changes to the red blood cells and as a result they become very stiff and sticky. This is very bad for the infected person because instead of flowing around the body like normal red blood cells, the infected cells become trapped in small veins and can no longer do their normal job. The ability of the parasite to redecorate red blood cells and make them stiff and sticky is what makes this type of malaria so dangerous, particularly when red cells get stuck in the brain. The research that we will do here will help us to understand the ways in which the malaria parasite sends out these sticky substances to the walls of red blood cells. Eventually, this will help us to find ways to stop the red blood cells from becoming sticky and prevent so many people from becoming very sick and dying with malaria.Read moreRead less
Decoding Conserved Mechanisms That Control Neuronal Migration
Funder
National Health and Medical Research Council
Funding Amount
$526,950.00
Summary
During brain development, nerve cells interact with each other and their surrounding environment through a forest of molecules that are essential for precise cellular communication. Deficient signaling between these molecules causes defects in development and leads to disease. By employing genetic and biochemical approaches we propose to identify new mechanisms through which the brain develops, to better understand how brain diseases such as epilepsy and schizophrenia occur.