The Bedford Stem Cell Research Foundation is proud to welcome six of the world leaders in stem cell research, neuroscience and neurosurgery:
Workshop Faculty
Douglas Kerr, MD, PhD
Associate Professor of Neurology,
Molecular Microbiology and Immunology
Director, John Hopkins Transverse Myelitis Center
John W. McDonald, MD, PhD
Director, International Center for Spinal Cord Injury
Kennedy Krieger Institute
Keith Tansey, MD, PhD
Director, Spinal Cord Injury Research
Shepherd Center
Steven L. Stice, PhD
Professor, GRA Eminent Scholar
Director of the Regenerative Bioscience Center at
University of Georgia
Scott Whittemore, PhD
Professor and Vice Chairman for Research
Department of Neurological Surgery
University of Louisville
Wise Young, MD, PhD
Professor, Department of Cell Biology and Neuroscience
Rutgers University
Director, W.M. Keck Center for Neuroscience
Invited Panel of Experts
Jose Cibelli, DVM, PhD
Professor, Department of Animal Science & Department of
Physiology, Michigan State University
Director, Cellular Reprogramming Laboratory
Philip J Horner, PhD
Assistant Professor of Neurological Surgery
University of Washington
Hans Keirstead, PhD
Associate Professor of Anatomy & Neurobiology,
University of California at Irvine
Reeve-Irvine Research Center
Ann A. Kiessling, PhD
Associate Professor of Surgery, Harvard Medical School
Director, Bedford Stem Cell Research Foundation
Douglas Kerr, MD, PhD
Research Biography
Dr. Kerr is an Associate Professor of Neurology with a joint appointment in the Department of Molecular
Microbiology and Immunology; and Cellular and Molecular Medicine. He specializes in transverse myelitis and multiple sclerosis. Dr. Kerr has established the Johns Hopkins Transverse Myelitis Center which is
the only such center in the entire world. The center utilizes the expertise of physicians and therapists from a variety of disciplines including neurology, neurosurgery, neuroradiology, rheumatology, rehabilitation medicine and urology for a comprehensive evaluation of transverse myelitis.
Dr. Kerr also has research interest in determining the cause(s) of transverse myelitis, evaluating novel markers to help prognosticate outcomes in the acute phase, and in developing novel treatments. Dr. Kerr also investigates neural stem cells as a potential tool for functional recovery in patients with transverse myelitis and motor neuron disease. He has made significant discoveries concerning the basic molecular biology of neuronal apoptosis, especially in motor neurons of the spinal cord.
Dr. Kerr’s laboratory research focuses on models of neuronal injury in the spinal cord. Using genetic and viral induced models of motoneuron injury, his laboratory has found that though there is an intrinsic abnormality within neurons, this abnormality is insufficient to induce death of that neuron. Rather, the surrounding astrocytes and microgial cells become deranged and “kill” the “at-risk” neuron. His research laboratory is now focused on elucidating the pathways involved in this killing. These findings are relevant to viral induced diseases of the CNS and to human motor neuron diseases such as ALS (amyotrophic lateral sclerosis) and SMA (spinal muscular atrophy).
Additionally, these models are utilized to examine the possibility of neuroregeneration. By transplanting a variety of human and mouse stem cells into the spinal cord, a partial restoration of function can be facilitated. The mechanisms underlying this functional recovery are varied and not completely understood. Dr. Kerr has also been interested in the endogenous response of spinal cord neural stem cells to paralysis. Interestingly, adult spinal cords DO have stem cells. Following viral-induced paralysis, they proliferate, presumably in an attempt to repopulate the spinal cord with those cells that just recently died. But it doesn’t happen: no new neurons are formed, and instead, the proliferating stem cells become shunted toward a glial fate. It is important to understand why these cells get “pushed” toward becoming glia and by modulating the fate specification of endogenous stem cells, perhaps the spinal cord can regenerate its own neurons rather than having to transplant them! This analysis will shed light on inherent biology of the spinal cord, and may have applications to human spinal cord diseases.
Dr. Kerr also directs The Johns Hopkins Project RESTORE, a multidisciplinary research and clinical collaboration emerging from The Johns Hopkins Transverse Myelitis and Multiple Sclerosis Centers to develop new diagnostic and therapeutic strategies in the treatment of neuroimmunologic disorders, such as multiple sclerosis (MS) and transverse myelitis (TM). Project RESTORE has three principle goals: to recover from acute attacks and illness; to stop progression of disease and disability; and to regenerate nerve cells and myelin.
Johns Hopkins Transverse Myelitis Center
John W. McDonald, MD, PhD
Dr. McDonald graduated from the University of Illinois, Champaign Urbana in 1985 with Bachelor’s of Science degree, magna cum laude, in Neuroscience. From there he matriculated at the University of Michigan, Ann Arbor, where he began a combined M.D./Ph.D. program in the Medical Scientists Training Program (MSTP) that he completed in 1992. While pursuing his advanced degrees, Dr. McDonald completed a fellowship in Neurology at the Johns Hopkins University School of Medicine and served as visiting scientist at Eli Lilly and Co in Indianapolis, IN. After receiving his M.D. and his doctorate, Dr. McDonald completed an internship in preliminary medicine at St. Joseph Mercy Hospital in Ann Arbor, MI. From 1993-1996, he completed his postgraduate training in adult Neurology at St. Louis’ Barnes Hospital and Washington University School of Medicine. Following his residency, Dr. McDonald joined the Washington University faculty in the Department of Neurology as an instructor in 1997, promoted to assistant professor of Neurology at Washington University School of Medicine. He also held co-assistant professorships in the School’s Departments of Neurological Surgery and Anatomy and Neurobiology.
In 1998, Dr. McDonald was named Medical Director of the Spinal Cord Neurorehabilitative Unit at Barnes-Jewish Hospital in St. Louis and Section Head of Spinal Cord Injury Program at Washington University. There he spearheaded development of what is now a leading spinal cord injury neuralrestoration program. It was there that he developed the “activity-based restoration” (ABR) therapies designed to help patients with long-term spinal cord injuries recover sensation, movement and independence; the therapy approached publically acknowledged as producing the substantial and delayed recovery of actor/activist Christopher Reeve.
Dr. McDonald joined Kennedy Kennedy Krieger Institute in 2004 in order to launch a brand-new spinal cord rehabilitation and research program with a focus on pediatric paralysis, a program that will become the only of its kind in the world. Dr. McDonald also holds a primary appointment as Associate Professor in the Department of Neurology at Johns Hopkins University School of Medicine with co-appointments in Physical Medicine and Rehabilitation and Neuroscience departments.
Dr. McDonald sits on the advisory boards of two companies, Restorative Therapies, Inc. of Baltimore, MD and BioAxone of Montreal, Canada. He is the present Chairman of the Spinal Cord Injury Research Program Advisory Board at the University of Missouri, Columbia and holds positions on the New York State SCI Research board, and the Philadelphia Shriner’s Hospital Medical Advisory Board.
Recent professional honors include being named Medical Director of the Year by insurer HealthSouth, receiving the SCI Research Inspiration Award from the Sam Schmidt Foundation and receiving the Reeve Research for Freedom Award from Gateway to a Cure.
Dr. McDonald’s research interests focus on the development of interventions to reduce spinal cord injury, promote remyelination, enhance regeneration and encourage recovery of function. In addition, Dr. McDonald is interested in studying the biology of embryonic stem cells, neural progenitor cells, mechanisms of oligodendrocyte death and glutamate excitotoxicity, mechanisms regulating myelination and the ontogeny of excitatory amino acid and related neurotransmitter pathways in the brain and their relationship to neurological disease.
Dr. McDonald also actively leads industry multi-center clinical trials in spinal cord injury repair, having completed 6 trials to date including the first human stem cell transplantation study with the company Diacrin. In addition to the completion of an ongoing project examining the efficacy of activity-based restoration in 60 adult patients with spinal cord injuries, Dr. McDonald and his team at the International Center for Spinal Cord Injury will soon launch a large prospective multi-center trial evaluating the efficacy of these therapies in pediatric patients in collaboration with the Philadephia Shriner’s Hospital.
Dr. McDonald’s research is increasingly focusing on approaches to regeneration and restoration of function in spinal cord injury and other disorders of paralysis using activity-base therapies. Such focus includes other regenerative approaches that have the potential of being translated into human therapies in the near-term.
The International Center for Spinal Cord Injury (ICSCI) at Kennedy Krieger
Keith Tansey, MD, PhD 
Dr. Keith Tansey joined Shepherd Center as Director of Spinal Cord Injury Research in 2008 and simultaneously was appointed to the Departments of Neurology and Physiology at Emory University School of Medicine and to the Spinal Cord Injury Clinic at the Atlanta VA Medical Center.
Dr. Tansey completed his B.S. and M.S. in Biology and Biomechanics at Stanford University and then completed his M.D. and Ph.D in Neuroscience at the University of Texas Southwestern Medical Center, where his dissertation research focused on spinal cord physiology. He completed his residency training in neurology at Washington University in St. Louis and then fellowships in spinal cord injury research and neurorehabilitation at Washington University and at the University of California Los Angeles. He returned to UT Southwestern and directed the Spinal Cord Injury Program there before he moved to Shepherd Center.
Dr. Tansey is board certified in Neurology and Spinal Cord Injury Medicine. He has won several teaching and research awards including one from the American Spinal Injury Association (ASIA) and he has presented his research work to the National Neurotrauma Society, the American Society for Neurorehabilitation, the Society for Neuroscience and at several international scientific meetings. Dr. Tansey also served as a Research Consortium Associate for the Christopher Reeve Paralysis Foundation.
Dr. Tansey is interested in neural plasticity and repair (re-training of remaining neural connections and generation of new neural connections) that leads to functional recovery after spinal cord injury and how those processes could be improved. He is specifically interested in neural circuits for motor functions like locomotion, but also neural circuits related to pain and autonomic nervous system function. He is working to combine interventions like activity based therapies with pharmacology, electrical stimulation, and even cellular transplantation to improve neural recovery after injury.
Dr. Tansey has combined animal model and human research to gain better insight into these questions and to more rapidly translate basic science research ideas into clinical studies.
The Shepherd Center
Steven L. Stice, PhD
Professor, GRA Eminent Scholar and Director of the Regenerative Bioscience Center at University of Georgia and CSO, Aruna Biomedical Inc.
Dr. Steven Stice has over 16 years of research and development experience in biotechnology and is a co-founder of five biotechnology companies. He was named one of the 100 Most Influential Georgians by Georgia Trend magazine. He produced the first cloned rabbit in 1987 and the first cloned transgenic calves in 1998 (George and Charlie). In 1997 his group produced the first genetically modified embryonic stem cell derived pigs and cattle. This research led to publications in Science and Nature journals, national news coverage (CBS, NBC, ABC and CNN) and the first US patents on cloning animals and cattle embryonic stem cells. In 2001, Dr. Stice announced the first cloned animal (calf) from an animal that was dead for 48 hours. In 2005, his stem cell group published the first work on deriving motor neurons from stem cells. Motor neurons are damaged lost during the progression of several diseases such as ALS and spinal muscular atrophy. Throughout his career he has published and lectured on cloning and stem cell technologies. Prior to joining the University of Georgia, Dr. Stice was a co-founder and Chief Scientific Officer at Advanced Cell Technology, a company developing cloning and stem cell technology.
Currently, Dr. Stice is a Professor and Director of the Regenerative Bioscience Center and has a Georgia Research Alliance Eminent Scholar endowed Chair at the University of Georgia. His research focuses on developing innovative stem cell technologies for curing diseases. He co-founded CytoGenesis, Inc., which was later purchased by BresaGen. Dr. Stice helped BresaGen develop three human embryonic stem cell lines approved for NIH funding.
He was named one of the top forty entrepreneurs under forty years old in Georgia (2000) and received the AGR grand president’s award for leadership and AGR Brother of the Century Award and outstanding Young Alumni Award from the University of Illinois. University of Georgia Research Foundation named Dr. Stice inventor of the year in 2005.
Dr. Stice received a B.S. in agricultural science at the University of Illinois in 1983. He then attended Iowa State University and completed a M.S. degree in 1985. Next, Dr. Stice went to the University of Massachusetts in Amherst for a Ph.D. program and graduated in 1989.
University of Georgia Center for Drug Discovery
Scott Whittemore, PhD
Research Description
Spinal Cord Injury causes many changes at the molecular level that damage or destroy key components of the nervous system that carry signals to and from the brain - including neurons, axons and the myelin coating that protects the nervous system much like the insulation around an electrical cord, as well as the vascular infrastructure that carries oxygen to these tissues.
The Molecular Neurobiology Laboratory focuses on strategies to replace lost neurons, help axons regenerate, and regeneration of the myelin coating around damaged or regenerating axons. Using undifferentiated precursor cells, gene therapies, and transplanted neurons, the lab seeks to understand the development of these key components of the vascular and nervous system at the molecular and genetic level in order to protect them from damage and/or promote their regeneration.
The general research focus of my laboratory is to utilize molecular and cellular biological techniques to address repair in spinal cord injury (SCI). These studies are usually initiated in vitro and successful approaches then taken into whole animal experiments. When designing strategies to facilitate functional restoration in SCI, three issues need to be considered: 1) replacement of lost neurons, 2) remyelination of de-myelinated and/or regenerating axons, and 3) inducing axotomized descending motor and ascending sensory axons to regenerate. We are utilizing multiple strategies to examine all three issues.
Neuronal replacement requires transplantation of exogenous neurons, as CNS neurons do not regenerate. Similarly, injury-induced de-myelination is secondary to a loss of intrinsic oligodendrocytes. Our approach to re-myelination is to transplant oligodendrocyte precursors into the demyelinated area. We are using CNS-derived stem cells as a source for both neurons and oligodendrocytes. Ongoing experiments in vitro are using retroviral vectors to infect the undifferentiated precursor cells with transcription factors that direct either neuronal or oligodendrocytic differentiation. Additionally, we isolate neuronal-restricted and glial-restricted populations of precursor cells. These cells are then engrafted into specific SCI models that deplete functionally discrete populations of neurons or endogenous oligodendrocytes in specific ventral motor pathways. We utilize a battery of behavioral and electrophysiological analyses to both characterize the initial deficits and determine the degree to which functional recovery is observed.
Our attempts to engender axotomized supraspinal, propriospinal, and sensory axons to regenerate takes a two-fold approach. We again use undifferentiated stem cells and genetically engineer them to express specific neurotrophic factors and/or cell surface molecules that facilitate regeneration by providing trophic support or a permissive substrate for regeneration. In these studies, we induce the stem cells towards an astrocytic phenotype in vivo, as early differentiating astrocytes are permissive for axonal outgrowth. Concomitant with the engraftment of these cells into the injured spinal cord, we use adenoviral or lentiviral vectors to deliver specific neurotrophic molecules at specific times post-injury to the cell bodies in the brainstem and/or into the spinal cord caudal to the injury site. This should enhance the regenerative capacity of the axotomized neurons and coax the regenerating fibers to leave the graft and enter the distal cord, respectively. In the second approach, we are characterizing in the injured spinal cord and brain the expression of the eph family of receptor tyrosine kinases and their ligands the ephrins. These molecules mediate repulsive interactions between cells that express receptor and ligand. We hypothesize that the expression of ephs and ephrins in the injured spinal cord may contribute to the non-permissive environment for regeneration. We have devised a number of reagents that can block the function of these molecules and are examining their effects on regeneration of specific ascending and descending fiber populations.
We recognize that no single strategy will be by itself effective in eliciting optimal regeneration in SCI. Our ultimate goal is to combine those individual strategies of ours and our colleagues here in the Department of Neurological Surgery that are effective to design interventive approaches that will result in functionally significant improvements after SCI.
Kentucky Spinal Cord Injury Reseach Center
Wise Young, MD, PhD
The Richard H. Shindell Chair in Neuroscience
Dr. Wise Young, founding director of the W.M. Keck Center for Collaborative Neuroscience and a professor at Rutgers, The State University of New Jersey, is recognized as one of the world's outstanding neuroscientists. He obtained a bachelor of arts degree from Reed College, a doctorate from the University of Iowa and a medical degree from Stanford University. After a surgery internship at New York University and Bellevue Medical Center, he joined the neurosurgery department at NYU. In 1984, he became director of neurosurgery research. In 1997, as part of Rutgers' commitment to the future, Dr. Young was recruited to establish and direct a world-class center for collaborative neuroscience.
Dr. Young was part of the team that discovered and established high-dose methylprednisolone (MP) as the first effective therapy for spinal cord injuries. This 1990 work upended concepts that spinal cord injuries were permanent, refocused research, and opened new vistas of hope. This team also played a major role in Andy Blight's signal work on 4-aminopyridine (4-AP), which shows significant promise for increasing nerve conductivity.
Dr. Young developed the first standardized rat spinal cord injury model used worldwide for testing therapies, formed the first consortium funded by the National Institutes of Health (NIH) to test promising therapies, and helped establish several widely accepted clinical outcome measures in spinal cord injury research.
Dr. Young founded and served as editor-in-chief of the Journal of Neurotrauma. He organized the National and International Neurotrauma Societies as forums for scientists to share discoveries and collaborate on spinal cord injury and brain research. He serves or has served on advisory committees for the NIH, the National Academy of Sciences, and NICHD, and has served on advisory boards for many spinal cord injury organizations.
Well-known as a leader in spinal cord injury research, Dr. Young has appeared on "20/20" with Barbara Walters and Christopher Reeve, "48 Hours," "Today," "Eye-to-Eye," Fox News and CNN's news magazine with Jeff Greenfield. His work has been featured in a Life magazine special edition, USA Today, and innumerable other news, talk and print presentations throughout the world. His honors include: NIH Jacob Javits Neuroscience Award (1985-1992), Wakeman Award (1991), Tall Texan of the Year Award (1997), ‘Cure’ Award (1998), Trustees Award for Excellence in Research (2001), Asian American Achievement Award (2002), Douglass Medal for work with the advancement of young women in the sciences (2003), and Elizabeth M. Boggs Award for service to the disability community (2004). In August 2001, TIME Magazine named Dr. Young as ‘America’s Best’ in the field of spinal cord injury research. In 2005 he was the first researcher elected to the Spinal Cord Injury Hall of Fame. Dr. Young was appointed to the Richard H. Schindell Chair in Neuroscience in 2006 by the Rutgers University Board of Governors.
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