Lee L. Eckhardt, MD

Position title: Assistant Professor, Medicine

Email: lle@medicine.wisc.edu

Phone: 608-265-4188

Organ System/Disease Focus:
Cardiac Arrhythmias; Inherited Sudden Death Syndromes
Aligned Research Focus:
induced pluripotent stem cells cardiomyocytes
Lee Eckhardt headshot

Pubmed

More Information:
Research Description:

Research work in my lab and my clinical practice focuses on the study and treatment of inherited arrhythmia syndromes. My particular interest is in potassium inward rectifiers (Kir2), which is the dominant component of IK1, and their contribution to cardiac sudden death, both from inherited and acquired arrhythmia syndromes. We use human induced pluripotent stem cells cardiomyocytes (iPS-CMs) to model inherited arrhythmia syndromes. One of my lab’s projects is to improve on current stem-cell technology to more closely model human cardiac cells with the use of IK1-enhanced cardiomyocytes. iPS-CMs are viable, reproducible and accessible cell model system to study a variety of cardiac conditions, testing for drug efficacy for cardiac medications or analysis of toxicity of potential therapeutics. However, because of the lack or minimal presence of IK1 in iPS-cardiomyocytes, my lab has been instrumental in creating an IK1-enhanced iPS- cardiomyocytes to improve the electrical maturity in order to model arrhythmias and disease. These disease models are used to study arrhythmia mechanisms to better understand the clinical disease process, with the ongoing goal of creating tailored drug therapy for sudden death prevention and improve on the usefulness of iPS-CMs for drug safety testing.

Selected References:
  • Vaidyanathan R, Markandeya YS, Kamp TJ, Makielski JC, January CT, Eckhardt LL. IK1-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromes. Am J Physiol Heart Circ Physiol. 2016 Jun 1;310(11):H1611-21. doi: 10.1152/ajpheart.00481.2015. Epub 2016 Apr 8. PMID: 27059077