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Frederica Montanaro , Ph.D.
Assistant Professor
Nationwide Children’s Hospital
Department of Pediatrics
Center for Gene Therapy WA-3020
700 Children’s Drive
Columbus, OH 43210
Phone: (614) 722-2875
Fax: (614) 722-5893
Email:
Federica.montanaro@nationwidechildrens.org
Education & Training:
McGill University, Montreal, QC Canada, 1991 BSc in Biology and
Neuroscience
McGill University, Montreal, QC Canada, 1999 Ph.D. in Biology
and Neuroscience
Harvard Medical School, 2005 Postdoctoral Fellowship
Research Interest:
My laboratory is interested in muscle regeneration and in the
development of cell-based therapies for muscular dystrophy disorders, in
particular Duchenne Muscular Dystrophy. On one hand, we are studying in
vitro models of muscle regeneration to identify genes and pathways that
are important for the activation of muscle stem cells and their participation
in muscle repair. We are using a combination of gene expression arrays
and RNA interference to identify and characterize genes of interest. On
the other hand, we have identified stem cells from the adult skin that
are able to participate in muscle repair following vascular delivery. We
are now optimizing the transplantation parameters and further characterizing
these cells to improve the efficiency with which they repair dystrophic
muscles.
Selected Publications:
- Montanaro F., Lindenbaum M. H., Carbonetto S. (1999) a-dystroglycan
is a laminin receptor involved in extracellular matrix assembly on
myotubes and muscle cell viability. J. Cell Biol. 145: 1325-1340.
- Montanaro F.and Carbonetto S. (2000) Developmental
biology of synapse formation. Encyclopedia of Life Sciences. http://www.els.net/
- Montanaro F. and Carbonetto S. (2003) Targeting dystroglycan in the
brain. Neuron 37(2):193-196.
- Montanaro F., Liadaki K., Volinski J., Flint A., Kunkel L.M. (2003)
Skeletal muscle engraftment potential of adult mouse skin side population
cells. Proc. Natl Acad. Sci. 100:9336-9341.
- Montanaro F., Liadaki K., Schienda J., Flint A., Gussoni E., Kunkel
L.M. (2004) Demystifying SP cell purification: viability, yield and
phenotype are defined by isolation parameters. Exp. Cell Res. 298:
144-154.
- Guyon J.R., Mosley A.N., Jun S.J., Montanaro F., Steffen L.S., Zhou
Y., Nigro V., Zon L.I., Kunkel L.M. (2005) Delta-sarcoglycan is required
for early Zebrafish muscle organization. Exp. Cell Res. 304: 105-115.
- Liadaki K., Montanaro F. and Kunkel L.M. Cellular-mediated delivery:
the intersection between regenerative medicine and genetic therapy.
In “Duchenne muscular dystrophy: Advances in therapeutics”.
Editors Rando T. and Chamberlain J. 2006.
- Kaspar, R.W., Allen, H.D. and Montanaro, F. (2009). Current understanding
and management for dilated cardiomyopathy in Duchenne and Becker muscular
dystrophy. Journal of the American Academy of Nurse Practitioners, 21:241-249.
- Kaspar RW, Allen HD, Ray WC, Alvarez CE, Kissel JT, Pestronk A, Weiss RB, Flanigan KM, Mendell JR, Montanaro F. (2009). Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy. Circ Cardiovasc Genet, 2:544-551.
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