University of South Carolina Home Page
University of South Carolina Home Page Future Students Current Students Alumni Faculty & Staff Patients
Courses
Areas of Interest
News
Faculty
Graduate Program
Helpful Links
Instrumentation Resource Facility
Seminars
Home

Sue Lessner

Sue Lessner, Ph.D.


Title:

Assistant Professor

PUBMED Link:

Lessner SM

Research:

Dr. Lessner's research interests center on vascular remodeling and angiogenesis (new blood vessel growth) in the contexts of atherosclerosis and tissue engineering. Vascular remodeling can be defined as any lasting change in the diameter, thickness, or structure of a mature blood vessel. In atherosclerosis, vascular remodeling acts as a compensatory mechanism to preserve blood flow in the face of plaque growth, which tends to cause stenosis or narrowing of the artery. However, vascular remodeling in atherosclerotic arteries has been correlated pathologically with plaque rupture, which leads to adverse clinical events such as heart attack and stroke. I am particularly interested in the role of matrix metalloproteinases (MMPs) in vascular remodeling and plaque vulnerability. MMPs are a class of enzymes which can degrade the extracellular matrix. We have shown in a mouse model of atherosclerosis that one of these enzymes, MMP-9, is required for vascular remodeling. Control of vascular remodeling is also important to the field of cardiovascular tissue engineering, since, once implanted in the body, engineered constructs are subject to the same types of cellular interactions as native tissues.

Another phenomenon which contributes to destabilization and rupture of atherosclerotic lesions is plaque angiogenesis. Like tumors, atherosclerotic plaques become hypoxic as they increase in thickness, due to oxygen transport limitations to the central core of the lesion. Tissue hypoxia promotes angiogenesis, or growth of new capillaries into the oxygen-starved region. I am interested in understanding both the fundamental biology of angiogenesis within atherosclerotic lesions as well as how angiogenesis contributes to plaque instability, using both in vitro and in vivo approaches. I use confocal microscopy and other imaging modalities available through the Instrumentation Resource Facility to assess vascularization both in atherosclerotic lesions and in subdermal implants in mouse models.


Recent Publications:

  • E. Ivan, J. Khatri, C. Johnson, R. Magid, D. Godin, S. Nandi, S. M. Lessner, and Z. S. Galis, “Expansive Arterial Remodeling Is Associated with Increased Neointimal Macrophage Foam Cell Content. The Murine Model of Macrophage-rich Carotid Artery Lesions,” Circulation, 105, 2686-2691 (2002).
  • S. M. Lessner, H. L. Prado, E. K. Waller, and Z. S. Galis, “Atherosclerotic Lesions Grow Through Recruitment and Proliferation of Circulating Monocytes in a Murine Model,” Am. J. Pathol., 160, 2145-2155 (2002).
  • J. J. Khatri, C. Johnson, R. Magid, S. M. Lessner, K. M. Laude, S. I. Dikalov, D. G. Harrison, H.-J. Sung, Y. Rong, and Z. S. Galis, “Vascular Oxidant Stress Enhances Progression and Angiogenesis of Experimental Atheroma,” Circulation, 109, 520-525 (2004).
  • C. Johnson, H.-J. Sung, S. M. Lessner, M. E. Fini, and Z. S. Galis, “Matrix Metalloproteinase-9 Is Required for Adequate Angiogenic Revascularization of Ischemic Tissues. Potential Role in Capillary Branching,” Circ. Res., 94, 262-268 (2004).
  • S.-H. Kim, S. M. Lessner, Y. Sakurai, and Z. S. Galis, “Cyclophilin A as a Novel Biphasic Mediator of Endothelial Activation and Dysfunction,” Am. J. Pathol., 164, 1567-1574 (2004).
  • S. M. Lessner and Z. S. Galis, “Matrix Metalloproteinases and Vascular Endothelium-Mononuclear Cell Close Encounters,” Trends Cardiovasc. Med., 14, 105-111 (2004).
  • S. M. Lessner, D. E. Martinson, and Z. S. Galis, “Compensatory Vascular Remodeling during Atherosclerotic Lesion Growth Depends on Matrix Metalloproteinase-9 Activity,” Arterioscl. Thromb. Vasc. Biol., 24, 2123-2129 (2004).
  • H.-J. Sung, C. E. Johnson, S. M. Lessner, R. Magid, D. N. Drury, and Z. S. Galis, “Matrix Metalloproteinase (MMP)-9 Facilitates Collagen Remodeling and Angiogenesis for Vascular Constructs,” Tissue Eng., 11, 267-276 (2005).
  • S. Ito, H.-W. Kim, O. Nakagawa, S. M. Lessner, K. Akram, M. Ushio-Fukai, and T. Fukai, “Antioxidant-1 (Atox1): A Novel Copper Dependent Transcription Factor Involved in Cell Proliferation,” (submitted - in revision).

Education:

  • 1983 B.S.E. Chemical Engineering Princeton University, Princeton, NJ
  • 1984-1987 Staff Scientist, Giner, Inc., Waltham, MA
  • 1988-1995 Research Assistant/Teaching Assistant, Dept. of Chemical Engineering, Massachusetts Institute of Technology, Cambridge
  • 2000 Ph.D. Chemical Engineering Massachusetts Institute of Technology, Cambridge
  • 2000-2003 Postdoctoral Fellow, Division of Cardiology, Emory University School of Medicine, Atlanta, GA
  • 2004 Instructor, Coulter Dept. of Biomedical Engineering, Emory University School of Medicine

Contact Information:

Email: lessner@gw.med.sc.edu
Phone: 803-733-1503
Address: Building1 Room C-38
USC School of Medicine
Columbia, SC 29209

Directory Map Events VIP Site Information