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Paxillin regulation of the integrin-cytoskeletal link

Reference	BB/D013011/1
Principal Investigator / Supervisor	Professor Nicholas Brown
Co-Investigators / Co-Supervisors
Institution	University of Cambridge
Department	Physiology Development and Neuroscience
Funding type	Research
Value (£)	242,294
Status	Completed
Type	Research Grant
Start date	01/02/2006
End date	31/12/2009
Duration	47 months

Abstract

Cell adhesion to the extracellular matrix plays a vital role in the development and life of multicellular organisms. Integrins are the primary receptors for the extracellular matrix, and once bound, they organise the cytoskeleton within the cell and transmit intracellular signals. The connection between the cytoplasmic domain of integrins and the cytoskeleton is made by a surprisingly large multiprotein complex. Our research is focused on understanding the mechanism of this integrin-cytoskeletal link, and how it is regulated during development. This will give insight into how proteins on the cell surface control cell and tissue morphogenesis and how multiprotein complexes are assembled by transmembrane proteins and regulated. Learning to control integrin adhesion has the additional benefit of providing ways to regulate blood clotting and immune function, as well as control cell interactions and cell shape changes during wound healing and tissue repair. A number of cytoskeletal adaptors are required within the integrin-cytoskeletal linking complex to make a strong link between integrins and the cytoskeleton. A second group of proteins appears to be involved primarily in the negative regulation of this complex. One negative regulator, paxillin, is thought to play a central role, by providing a scaffold for protein interactions that can be regulated by multiple signalling pathways. The importance of disassembing adhesion sites is clear in migrating cells, but it is not yet known why negative regulators such as paxillin are also found to be part of stable integrin adhesive junctions, such the sites of attachment of muscles to the tendon matrix. The model organism Drosophila provides us with an excellent system to test the function of paxillin in a variety of different kinds of integrin-mediated events. There is a single paxillin gene in Drosophila, compared to 3 paralogues in vertebrates, making it easier to completely remove paxillin gene function from the animaland study the consequences. Core functions of these key adhesion molecules are likely to be conserved between vertebrates and Drosophila, so that our application of the genetic tools in Drosophila will reveal basic functions of the paxillin family. We have generated a null allele in the paxillin gene, which provides us with the opportunity to determine the essential functions of paxillin within this organism. We propose to use this mutant to discover if paxillin does act primarily as a negative regulator of integrin adhesion, and how such negative regulation contrbutes to the function of stable integrin junctions. Experiments will be performed to elucidate whether a short version of paxillin, produced from an alternative transcriptional start, works to balance the negative action of paxillin by inhibiting its function. The role of tyrosine phosphorylation in regulating paxillin function will be analysed by assaying the ability of mutant forms of paxillin lacking specific tyrosines to function within the organism. Once we have identified key regulatory tyrosines, we will use genetic approaches to identify the potentially new regulatory pathways involved. Finally, we will examine the factors that contribute to the recruitment and maintenance of paxillin at sites of adhesion.

Summary

The mechanism that keeps the individual units that make up our body, or cells, attached together is known as cell adhesion. Thus, cell adhesion forms the 'glue' that holds cells together, and is of two types. In the first type, cell adhesion proteins on the surface of one cell bind directly to similar proteins on the surface of the adjacent cell. In the second type, which is the focus of this research, cell adhesion proteins on the surface of the cell, called integrins, bind to a network of proteins outside the cell, the extracellular matrix. Extracellular matrix proteins are made by the surrounding cells, transported outside, and assembled into a stable network. In many cases this matrix forms between two layers of cells and is used to link the two together, as the integrins in each layer bind to the same intervening extracellular matrix. An example of this is the link between two layers in our skin, the epidermis and the dermis. If the adhesion mechanism is faulty, then the two layers separate, resulting in a blister. Not only do integrins need to bind tightly to the extracellular matrix, but they also cross the membrane that forms the outer surface of the cell, and connect to proteins inside the cell. The portion of the integrin inside the cell provides an anchor for the assembly of a complicated linking structure, composed of many proteins building blocks, that connects integrins to the fibres within the cell, the cytoskeleton, that dictate cell shape, like reinforcing rods within cement. Recent findings have shown that some of the proteins within the linking structure act by taking the structure apart again. One of these proteins is called paxillin, which coordinates the activities of the proteins involved in the disassembly of the link between integrins and the cytoskeleton. Paxillin works as a scaffold that holds many proteins together, like the stem of a bunch of grapes. Being able to turn integrin adhesion off is important for cells that crawl over the extracellular matrix, as portions of the cell surface at the front of the cell stick to the matrix, so that the cytoskeleton can move the cell over these attachment points, and then the attachment must be broken down at the rear of the cell so that the cell can continue to move. The goal of this research is to discover more about how paxillin and the disassembly proteins work and how they are used in different ways in the development of an organism from a single cell, the fertilised egg. These different ways include directing cell movements around the developing embryo, permitting cells to take on special abilities, and forming stable points of strong adhesion between cell layers. As these are complex problems, we have chosen a simple animal to study, the fruit fly Drosophila, so that we have the best chance of solving them. Fruit flies use integrins in the same way as we do, as exemplified by the fact that faulty integrins in the fly also cause blisters. We aim to discover the basic mechanisms of paxillin function that are shared between all animals. In future, we will be able to apply this knowledge to the treatment of medical conditions arising from defects in integrin function, which include skin blistering diseases and aberrant blood clotting, as well as diseases where integrin activity makes the illness worse, for example by helping cancerous cells move around the body.

Committee	Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics	Immunology
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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