Timothy J. Kamp
Position title: Professor - Medicine; Co-director - Stem Cell and Regenerative Medicine Center
Email: tjk@medicine.wisc.edu
Phone: Phone: (608) 263-1172, (608) 263-1532
Address:
ORGAN SYSTEM/DISEASE FOCUS - Cardiac, ischemic heart disease, heart failure, arrhythmias
ALIGNED RESEARCH FOCUS - Cardiogenesis from embryonic stem cells
Address: 8459 WIMR II – 1111 Highland Ave. – Madison, WI 53705
News Releases:
- Stem cell ‘heart patch’ moves closer to clinic 21 September 2016
- New stem cell technique promises abundance of key heart cells; 28 May 2012
- Heart cells derived from stem cells used to study heart diseases; 9 May 2011
- UW-Madison Heart Stem Cell Study Among Top Research Advances; 22 January 2010
Education
B.S. magna cum laude, 1978-1982, University of Notre Dame, Notre Dame, Indiana, Preprofessional Studies
M.D. cum laude, 1982-1989 University of Chicago, Pritzker School of Medicine, Chicago, Illinois
Ph.D., 1982-1989, University of Chicago, Department of Pharmacological & Physiological Sciences
Internal Medicine Resident, 1989-1991, Osler Medical Service, Johns Hopkins Hospital, Baltimore, MD
Cardiology Fellow, 1991-1996, Johns Hopkins Hospital, Baltimore, MD
Research
Our research focuses on embryonic stem cells (ESCs) and their applications to cardiovascular research and potentially cardioregenerative medicine. Our initial work with human ESCs demonstrated that these cells differentiate in embryoid bodies to form spontaneously contracting cardiomyocytes. Electrophysiological characterization of the hESC-derived cardiomyocytes revealed that different types of cardiomyocytes differentiate including atrial, ventricular and nodal type cells. Current research is focused on understanding cardiogenesis in the ES cell system and harnessing this process to efficiently obtain defined populations of hESC-derived cardiomycytes. The human cardiomyocytes obtained from hESCs provide a powerful system to create disease models and to evaluate the cellular electrophysiological and functional properties of human cardiomyocytes at different stages of development. Other projects in the laboratory examine the use of ESCs and their derivatives in cellular therapies for heart disease. Myocardial infarction models in mice and large animals have been developed to pilot cellular therapies first employing mouse ESCs and derivatives. Our initial studies have provided proof of principal evidence that mouse ESCs can induce regeneration in infarcted mouse heart. Ongoing research focuses on identifying optimal cellular populations derived from ESCs for cardiac therapy, determining the best delivery strategies, and overcoming challenges related to immune rejection of allogeneic cells.