B.Sc. (Hons) Biochemistry/Microbiology, University of Leeds. 1980
Ph.D. Biochemistry, University of London. 1984
MRC project Grant Holder, Dept. of Physiological Sciences, University of Newcastle upon Tyne (1988-1990).
Lecturer, Dept. of Physiological Sciences, University of Newcastle upon Tyne (1990-1997).
Senior Lecturer, Dept. of Physiological Sciences, University of Newcastle upon Tyne (1997-2001).
Elected member of The Physiological Society in 1992; Biophysical Society in 1993; American Physiological Society in 1995; Society of General Physiologists in 1996.
Committee member of The Physiological Society and chairman of the Education and Information sub-committee (1997-2001). Member of the Meetings Advisory Committee of The Physiological Society 2003-2005
Currently Theme convenor of the Epithelial and Membrane Transport Theme of the Physiological Society (2010- )
Editor for Experimental Physiology (1999 - 2006).
Member of the Scientific Advisory Committee of the European Cystic Fibrosis Society (2002).
Member of the Research and Medical Advisory Committee of the Cystic Fibrosis Trust (2001- 2004).
Member of the steering committee of the UK CF Microbiology Consortium 2005- 2008.
Deputy Chairman of the Research Advisory Committee of the CF Trust (2004 - 2013).
Currently Chair of the Stategic Implementation Board of the CF Trust (2013 - )
The major research interest of our lab is to understand the cellular mechanisms that orchestrate epithelial ion, fluid and mucus secretion in differentiated adult epithelial tissues, and how epithelial dysfunction impacts on the pathogenesis of chronic diseases such as cystic fibrosis and asthma.
Epithelial ion (salt) transport is a fundamental function of all epithelial tissues and determines whole body fluid volume, blood pressure and acid-base balance, as well as regulating absorption and secretion of fluid and macromolecules such as digestive enzymes and mucus. Numerous diseases are caused by aberrant epithelial ion transport such as hypertension, cholera, polycystic kidney disease and cystic fibrosis, the most common, life-shortening, inherited disease in the white population. Understanding which transport proteins are involved, how they coordinate ion and fluid transport by the cell, and what goes wrong in disease is vitally important, not only for a better understanding of the biology of the system but also in developing new treatments to combat major diseases.
Current projects are concerned with regulation of CFTR, the ion channel whose dysfunction causes cystic fibrosis, by the luminal microenvironment, role of CFTR and SLC26A anion transporters in co-ordinating pancreatic and airway bicarbonate and mucus secretion and the novel role of environmental CO2 in cell signalling and transport defects in the kidney and airways.
We use a multidisciplinary approach employing a range of molecular, biochemical and cell physiological techniques. Much of our work is conducted at the cellular level but employs native tissue and cells as much as possible.
Work has been funded by The Wellcome Trust, The Cystic Fibrosis Trust, The Royal Society, Kidney Research UK, Northern Counties Research Trust, AFLM, BBSRC and the MRC
Patch clamp electrophysiology
Ion channel reconstitution
Stage 1 Medical
Stage 1 Biomedical Science
Stage 2 Biomedical Science
Stage 3 Biomedical Science