Hansell H. Stedman

faculty photo
Associate Professor of Surgery
Attending Surgeon, Hospital of the University of Pennsylvania, Philadelphia, PA
Attending Surgeon, Veteran Affairs Medical Center, Philadelphia, PA
Director, Muscular Dystrophy Research Institute for Human Gene Therapy, University of Pennsylvania School of Medicine, Philadelphia, PA
Ad Hoc Reviewer of Grants for Medical Biochemistry and Skeletal Muscle Biology study sections and Special Emphasis Panel study section, National Institutes of Health, Bethesda, MD
Department: Surgery
Graduate Group Affiliations

Contact information
709A Stellar Chance Labs
422 Curie Blvd.
University of Pennsylvania
Philadelphia, PA 19104-6069
Office: 215-898-1432
Fax: 215-573-8606
B.S. (Chemistry and Biology)
Massachusetts Institute of Technology, 1979.
Harvard University, 1984.
Post-Graduate Training
Intern in Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA, 1984-1985.
Resident in Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA, 1985-1986.
Post Doctoral Fellow, Harrison Department of Surgical Research, University of Pennsylvania School of Medicine, Philadelphia, PA, 1986-1987.
Post Doctoral Fellow, Department of Human Genetics, Cell & Developmental Biology, and Pathobiology, University of Pennsylvania School of Medicine, Philadelphia, PA, 1987-1989.
Resident in Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA, 1991-1994.
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Description of Research Expertise

Research Interests
- Genetics & Comparative Genomics – Contractile Proteins
- Integrative Biology –Skeletal & Cardiac Muscle
- Pathobiology & Therapy – Muscular Dystrophy & Cardiomyopathy
- Vascular Approaches to Systemic Gene Delivery

Key words: Muscular Dystrophy, Integrative Biology, Myosin, Gene/Molecular Therapy, Cardiomyopathy, Comparative Genomics.

Description of Research
Most of the projects in the laboratory trace back to an underlying focus on heritable and acquired diseases affecting muscle. A recent spin-off illustrates some of the excitement and unpredictability of basic research.

As the central force-generating protein of all types of muscle, myosin can be viewed as the raison d'être for the supporting molecular machinery of muscle. An understanding of this protein, its evolutionary constraints, and its interaction with other key components of the contractile apparatus and cytoskeletal network is essential to the study of muscle disease. We have studied all of the human genes for conventional muscle myosins with the surprise finding that one of them has been mutated in a recent direct human ancestor. The temporal correlation of this mutation with the emergence of the genus Homo has provided fuel for a wide range of collaborative projects in integrative biology.

Most of the mutations implicated in the human muscular dystrophies have been mapped to genes encoding proteins involved in adhesive links between the contractile apparatus and the extracellular matrix. The myosin motors are fine, but the myocytes degenerate because the dysfunctional adhesive link disrupts cellular homeostasis as the muscles generate force. Although the mechanisms are not fully understood, gene transfer technology has been essential for dissecting the components of this system. Through this process there have recently emerged a range of interesting opportunities for translational research directed at the goal of clinical therapy. Widespread gene delivery has been a rate-limiting step in this process. The lab has made substantial progress in this area by applying novel developments in microvascular physiology and endothelial cell biology to the problem at hand. Safety studies suggest a feasible pathway to clinical therapy for muscular dystrophies, with spin-offs relevant to a spectrum of cardiac muscle and non-muscle diseases.

Rotation Projects
1. Gene Transfer for Duchenne Muscular Dystrophy
2. Molecular Evolution of Myosin Motors
3. Pathophysiology of Skeletal and Cardiomyopathy
4. Mechanisms of Morphological Change During Speciation

Lab personnel:
Kapil Gopal, M.D., Postdoctoral Fellow
Marilyn Mitchell, Research Specialist
Ben Kozyak, Pre-doctoral Student
Zhonglin Wang, M.D., Research Specialist
Xiaoqing Zheng, M.D., Visiting Scientist
Pan Pan Wang, Pre-doctoral Student

Description of Itmat Expertise

Dr. Stedman's studies pertain to genetics and disease mechanisms in Duchenne and limb-girdle muscular dystrophies.

Selected Publications

Toromanoff, Alice. Cherel, Yan. Guilbaud, Mickael. Penaud-Budloo, Magalie. Snyder, Richard O. Haskins, Mark E. Deschamps, Jack-Yves. Guigand, Lydie. Podevin, Guillaume. Arruda, Valder R. High, Katherine A. Stedman, Hansell H. Rolling, Fabienne. Anegon, Ignacio. Moullier, Philippe. Le Guiner, Caroline.: Safety and efficacy of regional intravenous (r.i.) versus intramuscular (i.m.) delivery of rAAV1 and rAAV8 to nonhuman primate skeletal muscle. Molecular Therapy: the Journal of the American Society of Gene Therapy 16(7): 1291-9, Jul 2008.

Moore, Steven A. Shilling, Christopher J. Westra, Steven. Wall, Cheryl. Wicklund, Matthew P. Stolle, Catherine. Brown, Charlotte A. Michele, Daniel E. Piccolo, Federica. Winder, Thomas L. Stence, Aaron. Barresi, Rita. King, Nick. King, Wendy. Florence, Julaine. Campbell, Kevin P. Fenichel, Gerald M. Stedman, Hansell H. Kissel, John T. Griggs, Robert C. Pandya, Shree. Mathews, Katherine D. Pestronk, Alan. Serrano, Carmen. Darvish, Daniel. Mendell, Jerry R.: Limb-girdle muscular dystrophy in the United States. Journal of Neuropathology & Experimental Neurology 65(10): 995-1003, Oct 2006.

Bridges, Charles R. Gopal, Kapil. Holt, David E. Yarnall, Charles. Cole, Steven. Anderson, Rochelle B. Yin, Xiaoqing. Nelson, Anthony. Kozyak, Benjamin W. Wang, Zhonglin. Lesniewski, James. Su, Leonard T. Thesier, Danielle M. Sundar, Hari. Stedman, Hansell H.: Efficient myocyte gene delivery with complete cardiac surgical isolation in situ. Journal of Thoracic & Cardiovascular Surgery 130(5): 1364, Nov 2005.

Su, Leonard T. Gopal, Kapil. Wang, Zhonglin. Yin, Xiaoqing. Nelson, Anthony. Kozyak, Benjamin W. Burkman, James M. Mitchell, Marilyn A. Low, David W. Bridges, Charles R. Stedman, Hansell H.: Uniform scale-independent gene transfer to striated muscle after transvenular extravasation of vector. Circulation 112(12): 1780-8, Sep 20 2005.

Arruda, Valder R. Stedman, Hansell H. Nichols, Timothy C. Haskins, Mark E. Nicholson, Matthew. Herzog, Roland W. Couto, Linda B. High, Katherine A.: Regional intravascular delivery of AAV-2-F.IX to skeletal muscle achieves long-term correction of hemophilia B in a large animal model. Blood 105(9): 3458-64, May 1 2005.

Krupnick AS, Zhu J, Nguyen T, Kreisel1 D, Balsara1 KR, Lankford EB, Clark CC, Levine S, Stedman HH, Shrager JB. : Inspiratory loading does not accelerate dystrophy in the mdx mouse diaphragm: Implications for regenerative therapy. Journal of Applied Physics 94(2): 411-19, Feb 2003.

Kim DK, Zhu J, Kozyak BW, Burkman JM, Rubinstein NA, Lankford EB, Stedman HH, Nguyen T, Levine S, Shrager JB: Myosin heavy chain and physiological adaptation of the rat diaphragm in elastase-induced emphysema. Respiratory Research 4: 1, 2003.

Konig S, Burkman J, Fitzgerald J, Mitchell M, Su L, Stedman H. : Modular organization of phylogenetically conserved domains controlling developmental regulation of the human skeletal myosin heavy chain gene family. Journal of Biological Chemistry 277(31): 27593-27605, Aug 2 2002.

Bridges CR, Burkman JM, Malekan R, Konig SK, Chen H, Yarnell CB, Gardner TJ, Stewart AS, Stecker M, Patterson T, Stedman HH. : Global cardiac-specific transgene expression using cardiopulmonary bypass with cardiac isolation. Annals of Thoracic Surgery 73(6): 1939-46, Jun 2002.

Dejardins P, Burkman J, Shrager J, Allmond L, Stedman H. : Evolutionary implications of three novel members of the human sarcomaric myosin heavy chain gene family. Molecular Biology & Evolution 19(4): 375-393, Apr 2002.

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Last updated: 02/26/2021
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