Beruflich Dokumente
Kultur Dokumente
BIOGRAPHICAL SKETCH
NAME POSITION
Professor of Experimental Pathology & Head of
Terence A. Partridge
Muscle Cell Biology Group
EDUCATION/TRAINING
DEGREE
INSTITUTION AND LOCATION YEAR(s) FIELD OF STUDY
(if applicable)
Heslop, L., Beauchamp, J.R., Tajbakhsh, S., Buckingham, M.E., Partridge, T.A., Zammit, P.S. (2001)
Transplanted primary myoblasts can give rise to functional satellite cells as identified using the
Myf5nlacZ/+ mouse. Human Gene Therapy, 8: 778-783.
Shefer, G., Partridge, T.A., Heslop, L., Gross, J.G., Oron, U. Halevy, O. (2002) Low-energy laser irradiation
promotes the survival and cell-cycle entry of skeletal muscle satellite cells. Journal of Cell Science,
115: 1461-1469.
De Val, S., Ponticos, M., Antoniv, T.T., Wells, D.J., Abraham, D., Partridge, T., Bou-Gharios, G. (2002).
Indentification of the key regions within the mouse pro- 2(I) Collagen gene far upstream enhancer.
Journal of Biological Chemistry, 277: 9286-9292.
Morgan, J.E., Pagel, C.N., Beauchamp, J.R., Gross, J.G., Fassati, A., . Thrasher, A.J., Di Santo, J.P.,
Abraham, D.J., Fisher, I.B, Shiwen, X., Partridge T.A. (2002). Myogenic cell proliferation and
generation of a reversible tumorogenic phenotype are triggered by pre-irradiation of the recipient site.
Journal of Cell Biology.157:693-702.
Zammit, P. S.; Heslop, L.; Hudon, V.; Rosenblatt, J. D.; Tajbakhsh, S.; Buckingham, M. E.; Beauchamp, J.
R., and Partridge, T. A. (2002) Kinetics of myoblast proliferation show that resident satellite cells are
competent to fully regenerate skeletal muscle fibers. Experimental Cell Research 15; 281: 39-49.
Wells, K. E.; Torelli, S.; Lu, Q.; Brown, S. C.; Partridge, T.; Muntoni, F., and Wells, D. J. (2003)
Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the
dystrophin associated protein complex in skeletal muscle. Neuromuscular Disorders. 13: 21-31.
Lu, Q-L, Bou-Gharios, G, Partridge, TA, (2003) Non-viral gene delivery in skeletal muscle: a protein factory.
Gene Therapy.; 10:131-142
Lu, Q-L, Liang, H-D, Partridge, T, Blomley, MJK (2003) Microbubble ultrasound improves the efficiency of
gene transduction in skeletal muscle in vivo with reduced tissue damage. Gene Therapy. 10: 396-
405
Lu, Q-L., Mann C. J., Lou, F., Bou-Gharios, G., Morris, G. E., Xue, S., Fletcher, S., Partridge, T. A. &
Wilton, S. D. Functional amounts of dystrophin produced by skipping the mutated exon in the mdx
dystrophic mouse. Nature Medicine 9, 1009 – 1014
ReimannJ, Brimah K, Schröder R, Wernig A, Beauchamp JR, Partridge TA. (2004). Pax7 distribution in
human skeletal muscle biopsies and myogenic tissue cultures. Cell Tissue Res. 315;233-243
Murtuza, B, Suzuki, K., Bou-Gharios, G., Beauchamp J. R., Smolenski , R. T., Partridge, T. A., Yacoub M.
H. Transplantation of myogenic precursors overexpressing interleukin-1 receptor antagonist
modulates adverse remodeling in infarcted murine myocardium: PNAS:101;4216–4221
Cousins J.C., Woodward K. J.,. Gross J.G .,. Partridge T. A., Morgan. J.E. Regeneration of skeletal muscle
from transplanted immortalised myoblasts is oligoclonal. J. Cell Sci. in press.
Ponticos, M., Abraham, D., Alexakis, C Lu, ., Q-L., Black C,, Partridge T. Bou-Gharios G. Col1a2 enhancer
regulates collagen activity during development and in adult tissue repair. Matrix Biology. (In press)
Ponticos, M., Partridge T., Black1, C. M.. Abraham D. J., Bou-Gharios G. Regulation of collagen type I in
vascular smooth muscle cells by competition between Nkx2.5 and deltaEF1/ZEB1. Mol Cell Biol, (in
press)
Zammit, P.S. ,Golding, J.P., Nagata, Y., Hudon, V., Partridge, T.A., Beauchamp, J.R. (2004) Muscle
satellite cells adopt divergent fates: a mechanism for self-renewal? Journal of Cell Biology (in press).
Peter S. Zammit†, Jaime J. Carvajal*, Jon P. Golding, Jennifer E. Morgan, Dennis Summerbell*, Terence
A. Partridge, Peter W. J. Rigby* and Jonathan R. Beauchamp Myf5 expression in satellite cells and
muscle spindles of adult muscle is controlled by separate genetic elements. Developmental Biology,
(in press)
C. Research Support
ONGOING RESEARCH:
The objective of this program is to integrate studies of cellular functions in the maintenance and
repair of skeletal muscle in vivo and in vitro so as to generate a coherent picture of the mechanims
involved.
PHS 398 (REV. 5/01) Biographical Sketch Format Page
Number pages consecutively at the bottom throughout the application. Do not use suffixes such as 3a, 3b.
Principal Investigator/Program Director (Last, first, middle):
This funding was specifically aimed at generating collaborative networks with other European
laboratories so as to facilitate collaborations on the study of myogenic stem cells.
This MDA funded project was aimed at finding new reagents to permit the identification and
characterization of the skeletal muscle satellite cell. We have identified a number of new markers
and have used them to demonstrate the behavioural heterogeneity of satellite cells.
This project is aimed at determining which cells in skeletal muscle are responsible for the fibrosis
that occurs in chronically injured muscle and the control elements of the collagen 1 gene that are
responsible for the excessive production of scar tissue in such muscles.
This European funding was directed at fostering cooperation between a number of laboratories
working on various aspects of aging in human and mouse skeletal muscle
This is one year of funding to establish a new technique for analyzing myogenicity of satellite cells
by transplanting them in very small numbers (5-10) on single isolated muscle fibres. We find that
under these conditions, satellite cells behave in a more ‘stem cell-like’ way than when they are
separated from the muscle fibre
This funding is specifically to foster the use of the single fibre transplantation technique for analysis
of myogenic cell behaviour using a number of transgenic markers that are available in mouse
colonies in laboratories at the Genethon and the Pasteur Institute.
This is a prestigious award of financial support to conduct work of collaboration for a total duration
of 1 year spread over a 2 year period. It is envisaged as involving the best Parisian laboratories
(Genethon and Institut Pasteur) and the home laboratory ( in this case my MRC laboratory during
2005 and the Children’s Hospital during 2006. The objective is to bring together the specialist
techniques of both sets of laboratories to gain previously unobtainable information on the nature of
the variety of cells that are grouped together under the name of satellite cell and to determine the
roles of these cell types in muscle repair after various types of injury.