News Release

MRC scientists advance understanding of cell death

Research carried out at University of Leicester

Peer-Reviewed Publication

University of Leicester

Medical Research Council (MRC) scientists have made an important advance in understanding the biological processes involved when cells are prompted to die. The work may help scientists to eventually develop new treatments for the many common diseases and conditions which occur when cell death goes wrong.

The research, published in leading journal Molecular Cell [1] today (Friday 14 August 2009) was carried out by a team of scientists, at the MRC Toxicology Unit at the University of Leicester and a subsequent patent application has been filed by MRC Technology, the commercial arm of the MRC.

Cells in the human body are continually dying and most of these cells kill themselves by a form of cell death, commonly referred to as apoptosis. In a healthy body, the number of cells stays constant. Millions of new cells are produced every second, and millions of others are lost or kill themselves. Failure of the normal apoptosis process plays a role in different diseases including cancer, certain neurodegenerative disorders such as Parkinson's and immune diseases, such as autoimmune lymphoproliferative syndrome (ALPS).

One of the study's authors, Dr Marion MacFarlane, MRC Toxicology Unit, explained: "This new research takes us a step closer to understanding how the DISC triggers cells to die. The challenge now is to try and use this fundamental knowledge to help work towards finding better treatments for conditions which occur when DISC-mediated cell death goes wrong."

Previous research has shown that a complex called the 'DISC', which is made up of different proteins and is formed following activation of molecules called 'Death Receptors', can trigger apoptosis by 'switching on' key players in the cell death process. However, previous research has found that the DISC can also activate cell survival, thus raising the question as to how paradoxically the 'DISC' can trigger these opposing cellular outcomes?

Now, scientists at the MRC Toxicology Unit have found that the DISC can trigger cell death or cell survival by switching the activity of key death-promoting molecules. Stopping the 'DISC' from functioning properly prevents the cell death programme from being carried out efficiently and instead results in cell survival. Thus, in diseases such as ALPS, where a crucial death-promoting protein is often not active the DISC fails to function properly.

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For further information and to arrange an interview with colleagues on this project, please contact Nicola Osmond-Evans in the MRC Press Office on 0207 670 5138 or press.office@headoffice.mrc.ac.uk

Notes to editors:

[1] "Reconstitution of the Death-Inducing Signalling Complex reveals a novel Substrate Switch that determines CD95-mediated Death or Survival" Molecular Cell

A copy of the Molecular Cell paper is available on request from Cathleen Genova at Cell Press on 001-616-397-2802 or cgenova@cell.com

The Medical Research Council is dedicated to improving human health through excellent science. It invests on behalf of the UK taxpayer. Its work ranges from molecular level science to public health research, carried out in universities, hospitals and a network of its own units and institutes. The MRC liaises with the Health Departments, the National Health Service and industry to take account of the public's needs. The results have led to some of the most significant discoveries in medical science and benefited the health and wealth of millions of people in the UK and around the world. www.mrc.ac.uk

About Medical Research Council Technology (MRCT) MRCT is the exclusive commercialisation agent for the UK Medical Research Council, working to translate cutting edge scientific discoveries into commercial products. MRCT bridges the gap between innovative basic science and making medicine. By providing drug-like candidate molecules to innovative new drug targets, we give pharmaceutical and biotechnology companies new starting points for drug discovery and development, based on MRC advances in science. www.mrctechnology.org

MRC press contact: 020 7637 6011 press.office@headoffice.mrc.ac.uk

University of Leicester Press Office Contact:
Ather Mirza
Press Office
Division of Marketing and Communications
University of Leicester
University Road
Leicester
LE1 7RH
tel: 0116 252 3335
email: pressoffice@le.ac.uk

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