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Prof Lucie Clapp
Room 324
Institute of Cardiovascular Science
Rayne Building, 5 University Street
Tel: 020 7679 6180
  • Professor Vascular Physiology
  • Centre for Cardiovascular Genetics
  • Institute of Cardiovascular Science
  • Faculty of Pop Health Sciences
I graduated with honours in Pharmacology from Bristol University in 1981 and studied for my PhD at St Georges' Hospital Medical School, London where I completed it in 1985. From there, I moved to the USA to pursue post-doctoral studies in the Physiology Department at the University of Massachusetts Medical School where I demonstarted neurotransmitter modulation of calcium and potassium channels in isolated gastric smooth muscle cells for the first time using the patch-clamp technique. Whilst there, I became an Instructor in Physiology and was awarded a Howard Sprague Postdoctoral Fellowship from the American Heart Association (AHA) for the best application in the in State of Massachusetts.

In 1988, I went back to the UK and worked in the Pharmacology Department at St Thomas' Hospital investigating ion channel regulation in the pulmonary circulation. In 1992, I was awarded a Wellcome Trust Career Development Fellowship and continued studies in the Cardiovascular Research Department on the vascular ATP-sensitive potassium (KATP) channels, demonstrating not only its presence but different biophysical properties to the channel descrbed in the heart and pancreas. At the same as being awarded a 5 year MRC Senior Fellowship to elucidate the role of potassium channels in septic shock, I moved to the Centre for Clinical Pharmacology, Department of, Medicine,UCL as a Senior Lecturer in 1996. My Fellowship was renewed in 2001, where the focus switched to calcineurin regulation of inwardly rectifying potassium channels, identifying this calcium-dependent phosphatase as a critical regulator of the KATP channel. In recognition of my research contribution, I was elected fellow of the AHA in 2001, appointed a Reader in Clinical Pharmacology in 2002 and subsequently awarded a personal chair as Professor of Vascular Physiology in 2005. I was elected Fellow of the Pulmonary Vascular Research Institute in 2010 for my work on prostacyclin pharmacology and cell signalling in the context of pulmonary hypertension, and a Fellow of the Society of Biology in 2011.

My international standing is recognised by publications in top peer-reviewed journals, including PNAS, Circulation Research, Lancet and Am J Respir Crit Care Med, editorials in Circulation Research and invitations to speak at symposia organised by the AHA, American College of Chest Physicians, European Respiratory Society, International Society for Heart and Lung Transplant, Intensive Care and Emergency Medicine and European Society of Cardiology. I am currently an editor for the British Journal of Pharmacology and peer review for numerous journals and also grant awarding bodies (Action Research, BBRSC, British Heart Foundation, Diabetes Foundation, Medical Research Council, Ireland Health Research Board, Dr Hadwen Trust, Wellcome Trust).

Experimental Medicine is at the forefront of my activities, and I have active links with hospital-based clinicians and scientists at the Royal Free (Prof Abraham and Dr Gerry Coghlan), GOSH (Prof Klein, Dr Schulze-Neick and Dr Moldina) and UCLH (Prof Singer and Dr Williams) as well as with Prof Morrell at Addenbrooke’s, Hospital Cambridge. I have been involved in the first clinical use of terlipressin in sepsis, the identification of a new clinical syndrome associated with drug-induced hyperkalemia and proof of concept of novel treatments for pulmonary arterial hypertension for which clinical trials are being set-up or are on-going. I have productive relationships (Consultancies, Research Grants) with several Pharma companies, including United Therapeutics, Pfizer, Cytokinetics, Bayer and GSK, and regularly provide information to market research companies (e.g. Adelphi Communications, Health Science Communications, Biopharm Insight).

Research Summary

Overall summary of research
In the last decade, our group has principally been involved in elucidating the biophysical and functional properties of vascular potassium channels with a strong emphasis on their roles in sepsis, vascular remodelling and pulmonary hypertension. Work has specifically focused on in vitro and in vivo models of septic shock in rodents and humans, the biochemistry and confocal imaging of calcineurin and its role in mediating smooth muscle proliferation as well as the mechanistic basis underlying the therapeutic effects of prostacyclins in pulmonary arterial hypertension (PAH). Complimenting these are studies in patients to establish biomarkers of early disease (smooth muscle hypertrophy) and the impact of prostacyclin therapy on a broader range of markers of endothelial dysfunction and inflammation in PAH.

Prostacyclin signalling through membrane and nuclear receptors
In collaboration with Prof Howarth and Dr Hall (ICH/GOSH) and Prof Morrell (Cambridge) we are exploring cellular mechanisms underlying abnormal cell growth in lung cells derived from patients with PAH in addition to the impact of prostacyclin therapy on this process. Interestingly, we have found in PAH that prostacyclin signalling is disrupted in pulmonary smooth muscle cells, switching away from the classical IP receptor and cyclic AMP driven pathway, to one involving the nuclear transcription factor, PPARy. The mechanism of PPARy activation by prostacyclin is unknown but we are exploring whether it inhibits growth through an impact on the NFAT/calcineurin pathway. In biochemical studies funded in partnership with United Therapeutics (USA) and Prof Whittle (William Harvey, Barts), we have very recently established that the prostacyclin analogue treprostinil has a novel pharmacology compared with other agents in its class like iloprost, activating both DP1 and EP2 receptors in the nanomolar range. These receptors therefore represent previously unrecognised targets for this agent, and suggest that the overall beneficial pulmonary vasorelaxant profile and other pharmacological actions of treprostinil, especially in diseases where the IP receptor is down-regulated, may contribute to its therapeutic efficacy. It remains to be determined how these findings impact on selexipag, a selective non prostanoid IP receptor agonist, currently in phase III clinical trials in PAH.

Calcineurin interaction with KATP channels

Our lab has been instrumental in showing that the calcium-dependent phosphatase, calcineurin is a key regulator of the ATP-sensitive potassium (KATP) channel. In collaboration with Prof Tinker (UCL and Barts and the London) we have shown that the molecular basis for this regulation involves dephosphorylation of channel subunits, and that such a mechanism, is likely to directly oppose the action of vasodilators which open this channel through phosphorylation. We and others have demonstrated that excessive opening of the vascular KATP channel is implicated in the vasodilation and vascular hyporeactivity that underlies septic shock, though despite this, therapeutic channel inhibition using sulfonylurea agents like glibenclamide has proved disappointing in humans. Our recent observations that sympathetic activity, which is often high in septic patients, may actually be helping maintain blood pressure by keeping the channel closed, could therefore explain lack of efficacy of channel inhibitors in sepsis. Studies in the future are planned to more fully understand the influence of sympathetic tone on in vivo KATP channel function and blood pressure, where the regulation may ultimately be determined by calcineurin activity.

Teaching Summary

I teach across 3 different Faculties at UCL on several BSc and MSc/MRes courses run in the Institute of Cardiovascular Science, Division of Medicine, Department of Neuroscience, Physiology & Pharmacology, and in Biochemistry. I am founder and director of the newly created IBSc in Cardiovascular Science, chair of the Exam Board for the equivalent MSc course and co-organiser of the 4 Year BHF PhD programme for which I am a co-applicant on the recent successful renewal of this PhD scheme in Aug 2016. Teaching activities are summarised below:

1. Integrated BSc in Cardiovascular Science for 3rd Year medical students
I have designed this course to give a contemporary scientific view of cardiovascular disease. Students will develop an understanding of the etiology, diagnosis and clinical management of common cardiovascular diseases through case-based, team work and class discussions. The course starts in Sept 2016. 

2. Heart & Circulation for 3rd year iBS/BSc (PHOL3002) and MSc (PHOLG043) students
I have been director of this module since 2013 and co-organise it with Prof Alun Hughes. Approximately 80 students take this highly popular course - a series of lectures (22 in total) and tutorials covering physiology and pathophysiology with special reference to the human heart and circulation. I run the lab-based organ bath pharmacology and blood pressure practicals and teach on a range of topics, including vascular potassium channels, smooth muscle contraction and animal models of cardiovascular disease. 

3.MSc in Cardiovascular Science
I lecture on animal models of pulmonary hypertension, including covering the genetic basis of this disease (CARDG02). I set in course essays and am on the teaching committee which oversees the course. 

4. BHF 4 Year PhD programme (since 2009)
For the next 5 years, 4 students will be appointed each year to engage in research in any area of cardiovascular biomedicine at UCL. I am involved in interviewing, mentoring, helping students choose appropriate rotation projects, and overseeing their 1st year assessments of each rotation project. 

5. 3rd Year BSc/iBSc students (PHOL3902 & PHOL3904)
This involves supervising laboratory research and library projects based around sepsis & pulmonary hypertension, examining student oral presentations and marking dissertations.

6. Biochemistry of Cardiovascular Disease (BIOC3011) & Cell Signalling in Health & Disease (PHOL3004)
I lecture on vascular remodelling in diseases such systemic hypertension and atherosclerosis and how endothelial dysfunction drives the pathophysiology (BIOC3011). In PHOL3004, I teach how the hormone prostacyclin can signal in cells through membrane and nuclear receptors. I set and mark in-course exam questions, and run a journal club. 

7. Drug Discovery (MEDCG004)
Includes lecturing on the pathobiology of pulmonary hypertension and the molecular targets for potential future novel treatments; the setting and marking of exam/essay questions.

8. International teaching
Teaching in symposia with CME (Continuing Medical Education) credits for organisations like the International Society for Heart and Lung Transplantation, American College of Chest Physicians and European Respiratory Society. Providing online materials to global pharmaceutical companies as well as to ACCME and companies including AKH Inc, both accreditation providers of continuing education for licensed health care specialists in the USA.

Academic Background
1985 PhD Doctor of Philosophy – Pharmacology University of London
1981 BSc Bachelor of Science – Pharmacology University of London
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