• University of Mannheim Featured PhD Programmes
  • Carlos III Health Institute Featured PhD Programmes
  • University of Leeds Featured PhD Programmes
  • London School of Economics and Political Science Featured PhD Programmes
  • University of Glasgow Featured PhD Programmes
  • University of Leeds Featured PhD Programmes
  • University of Leeds Featured PhD Programmes
University of Liverpool Featured PhD Programmes
University of Southampton Featured PhD Programmes
Imperial College London Featured PhD Programmes
University of Bristol Featured PhD Programmes
University of Manchester Featured PhD Programmes

Regulation of cardiac ion channels by carbon monoxide


Project Description

Carbon monoxide (CO) poisoning accounts for more than 50% of all fatal poisonings, and the organs most susceptible to damage are the heart and brain. While chronic CO exposure can induce myocardial injury and fibrosis, acute exposure is associated with a disruption of ventricular repolarization and prolongation of the QT interval (termed long-QT (LQT) syndrome), thereby predisposing affected individuals to arrhythmias and even sudden death.

We have shown that several cardiovascular ion channels are important targets for modulation by CO and their regulation can contribute to the pro-arrhythmic effects of this gas. For example, pro-arrhythmic / LQT-like effects of CO may be due, at least in part, to its ability to modulate the activity of Nav1.5 and hERG-1 (see further reading, below, and unpublished observations); inheritable mutations in these channels are known to cause LQT3 and LQT2 respectively. KCNQ1 encodes the a-subunit of the voltage-gated potassium channel KvLQT1 (also known as Kv7.1) that co-assembles with KCNE1 (a-subunit, also known as minK) in vivo to form channels that gives rise to IKs, the slow delayed rectifier K+ current which plays an important role in repolarization during phase 3 of the cardiac action potential. The importance of KvLQT1 is reflected in the fact that numerous inheritable mutations in KCNQ1 give rise to LQT1, the most common of the LQT syndromes.

In this multidisciplinary study we shall explore the modulation of IKs and other ion channels contributing to the cardiac action potential using a range of complementary cell biology techniques including patch-clamp electrophysiology, molecular biology and confocal laser-scanning microscopy. We will fully characterise the molecular mechanisms and structural requirements underlying CO-mediated regulation of these channels, and determine the significance of such modulation to arrhythmia generation. Our studies will therefore further develop our understanding of (and hence treatment of) CO-induced arrhythmias. The project will be co-supervised by Dr John Boyle and Professor Derek Steele.

Funding Notes

You should hold a first degree equivalent to at least a UK upper second class honours degree in a relevant subject. Candidate whose first language is not English must provide evidence that their English language is sufficient to meet the specific demands of their study, the Faculty minimum requirements are:
•British Council IELTS - score of 6.5 overall, with no element less than 6.0
•TOEFL iBT - overall score of 92 with the listening and reading element no less than 21, writing element no less than 22 and the speaking element no less than 23.

References

Dallas, M.L. et al. (2012) Am. J. Resp. Crit. Care Med.186, 648-656.
Boycott, H.E. et al. (2013). FASEB J. 27: 3395-3407.
Scragg, J.L. et al. (2008) J. Biol. Chem. 283, 24412-24419.

Email Now

Insert previous message below for editing? 
You haven’t included a message. Providing a specific message means universities will take your enquiry more seriously and helps them provide the information you need.
Why not add a message here
* required field
Send a copy to me for my own records.
Email Sent

Share this page:

Cookie Policy    X