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Systematic analysis of polarised trafficking during cell motility

Reference	BB/H002308/1
Principal Investigator / Supervisor	Dr Joshua Rappoport
Co-Investigators / Co-Supervisors
Institution	University of Birmingham
Department	Sch of Biosciences
Funding type	Research
Value (£)	337,425
Status	Completed
Type	Research Grant
Start date	01/10/2009
End date	30/03/2013
Duration	42 months

Abstract

The main goal of this project is to determine the role of vesicle trafficking in cell motility. The studies described in this proposal will test the hypothesis that polarised membrane trafficking is essential to cell migration. These studies will be performed in an inducible and medically relevant model for cell motility, epithelial wound healing. There are three general pathways involved in the insertion and retrieval of proteins at the plasma membrane (endocytosis, exocytosis and endosomal recycling). Furthermore, these can be separated into sub-pathways, such as clathrin-mediated endocytosis as opposed to clathrin-independent endocytosis. This project will systematically assess each potentially relevant trafficking process for functional importance in both the initiation and progression of cell motility (Aim 1). This will be done through expression of dominant negative mutants known to inhibit individual trafficking processes. Expression either before or after monlayer wounding will permit analysis of the role of each process on a phases of cell motility. Further studies will image markers for each process in live cells to evaluate whether polarised vesicle trafficking occurs during the production of the motile phenotype and/or once a steady-state rate of motility has been attained (Aim 2). The combination of imaging markers for each pathway, along with integrins, and in the context of dominant negative expression, will provide a complete analysis of the potential for polarised trafficking, mechanistically linking cargo, trafficking and motility. Importantly, preliminary data has been obtained which supports each step of this project. Finally, data from Aim 2 will be systematically analysed employing bioinformatic approaches. Thus, these studies will provide a complete understanding of the role of vesicle trafficking in cell motility.

Summary

Epithelial cells form a barrier between different compartments in the body. The outer layer of skin is formed from epithelial cells, and protects our internal organs from the external environment. A single layer of epithelial cells also separates the air space in our lungs from the blood vessels, and produces the barrier in the intestine across which digested food travels. When wounds form, such as cutting a finger on a kitchen knife, epithelial cells move by crawling forward to close up the newly exposed area. This crawling is referred to as cell motility. Improper wound healing can result in scar formation. With wounds to the skin, this might only pose a cosmetic issue; however, inside the body, this can be much more serious. One such medically relevant case can occur when dust and dirt is inhaled into the lungs. The small wounds to the epithelial barrier of the lung must properly heal, or a condition known as pulmonary fibrosis can result. If this occurs the epithelial layer across which oxygen is absorbed is replaced by scar tissue, which is not able to exchange gas properly. Thus, it is of great importance to understand the mechanisms that control epithelial cell motility, and this information could lead to the development of new treatments to promote wound healing and limit scar formation. Similar to the way our skin protects the inside of the body, the plasma membrane forms a barrier between the inside of cells, the cytosol, and the outside, extracellular, space. Many proteins reside in the plasma membrane and provide a linkage between the cytosol and extracellular space. These include channels and pumps that let specific substances into or out of cells, receptors for extracellular signals that cells send to each other, as well as adhesion proteins that permit cells to stick to each other, and the extracellular environment, or matrix. The number of these membrane proteins, as well as the activity and specific location within the plasma membrane, is controlled by a process known as vesicle trafficking. Vesicles are specialised carriers that transport cargo, such as membrane proteins, between different locations in the cell. The insertion of proteins into the plasma membrane occurs through exocytosis, while retrieval into the cytosol is achieved via endocytosis. Several different sub-pathways of exocytosis and endocytosis exist which can traffic specific cargo in response to particular cues. One main goal of this project is to determine which vesicle trafficking pathways are important in epithelial cell motility. Understanding of the trafficking of specific cargo could be harnessed to potentially stimulate wound healing. Techniques exist whereby a single vesicle trafficking process can be specifically inhibited, and by measuring subsequent effects on cell motility, particular pathways relevant to wound healing will be identified. Furthermore, through application of cutting edge microscopy we are able to image individual events of endocytosis and exocytosis, as well as the movement of single vesicles in the cytosol. This technology will be used to test the hypothesis that trafficking of cell adhesion proteins known as integrins from one area of the cell (e.g. the back edge) to another (e.g. the front edge) could drive cell motility. This will directly evaluate the 'polarised recycling model for cell motility', which suggests that back-to-front trafficking of adhesion proteins could drive a cell forward in a manner analogous to a tank tread. Finally, we will apply innovative computational approaches to analyse live-cell microscopy data to permit a systematic analysis of the role of vesicle trafficking in epithelial cell motility. Results stemming from this project could provide valuable information regarding the regulation of cell motility and could lead to the development of new therapies that could increase the rate of wound healing.

Committee	Research Committee D (Molecules, cells and industrial biotechnology)
Research Topics	X – not assigned to a current Research Topic
Research Priority	Systems Approach to Biological research
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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