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Ken
Knight
- Current research activities
At the Bernard O’Brien Institute of Microsurgery I am a
senior member of the tissue engineering research team, which has
developed and patented in vivo animal models of vascularized tissue
engineering using chambers in mice, rats, rabbits and pigs. Initially
we grew vascularized adipose tissue and skeletal muscle, by seeding
chambers with preadipocytes and myoblasts respectively, together
with extracellular matrix, growth/differentiation factors and,
importantly, blood vessels in continuity with the general circulation.
In collaboration with A/Prof. Paul Simmons, PMCI, we have used
both in vivo and in vitro models to differentiate bone marrow-derived
stromal precursor cells along adipogenic and myogenic pathways.
Two of my current interests are: (i) a study of extracellular
matrix components in soft tissues (notably adipose tissue) with
a view to developing “instructive” tissue engineering
scaffolds for use in these models, in collaboration with Dept
of Chemical & Biomolecular Engineering, University of Melbourne;
and (ii) the growth of endocrine “organoids” by seeding
in vivo tissue engineered constructs with pancreatic islets and/or
their precursors (in collaboration with Prof Len Harrison, WEHI)
or with pituitary stem cells (in collaboration with Dr Paul Thomas,
Murdoch Children’s Research Institute).
- Keywords
Tissue engineering, angiogenesis, adipogenesis, organogenesis,
islet transplantation, stem cells, extracellular matrix, basement
membrane.
- End-user applications
- Breast reconstruction
- Soft tissue reconstruction/repair
- Treatment of type 1 diabetes by islet “organoid”
transplantation
- Key publications
| I. |
Mian R, Morrison WA, Hurley JV, Penington AJ,
Romeo R, Tanaka Y, Knight KR (2000) Formation of new tissue
from an arteriovenous loop in the absence of added extracellular
matrix. Tissue Eng 6: 595-603. |
| II. |
Mian R, Knight KR, Penington AJ, Hurley JV, Messina A, Romeo
R, Morrison WA (2001) Stimulating effect of an arteriovenous
shunt on the in vivo growth of isografted fibroblasts: a preliminary
report. Tissue Eng 7: 73-80. |
| III. |
Cassell OCS, Morrison WA, Messina A, Penington AJ, Thompson
EW, Stevens GW, Perera JM, Kleinman HK, Hurley JV, Romeo R,
Knight KR (2001). The influence of extracellular matrix on
the amount and type of engineered tissue in an experimental
rat model. Ann NY Acad Sci 944: 429-442. |
| IV. |
Hofer SOP, Knight KM, Cooper-White JJ, O’Connor AJ,
Perera JM, Romeo-Meeuw R, Penington AJ, Knight KR, Morrison
WA, Messina A (2003). Increasing the volume of vascularized
tissue formation in engineered constructs. An experimental
study in rats. Plast Reconstr Surg 111: 1186-1192. |
| V. |
Cronin KJ, Messina A, Knight KR, Cooper-White JJ, Stevens
GW, Penington AJ, Morrison WA (2004) New murine model of spontaneous
autologous tissue engineering, combining an arteriovenous
pedicle with matrix materials. Plast Reconstr Surg
113: 260-269. |
- Outreach activities
None as Yet.
- Key organisation membership
TEAM VIC
- Early career researcher?
No.
- Young investigator?
No.
- Skills and expertise
- Isolation and purification of extracellular matrix molecules
(proteomics including column chromatography, FPLC, SDS-PAGE,
Western analysis, etc).
- Experimental surgery (animal models)
- Cell culture and cell isolation techniques
- Chemical pathology (enzyme assays, RIAs, ELISAs) 
- Histopathology (notably immunohistochemistry)
- Specialist equipment and infrastructure
- Operating microscopes in the Experimental Medicine & Surgery
Unit (animal research facility)
- DAKO autostainer for immunohistochemistry
- Contact Details
Dr Ken Knight
Bernard O’Brien Institute of Microsurgery and Department
of Surgery, St. Vincent’s Health University of Melbourne
Address: 42 Fitzroy Street Fitzroy, Victoria 3065
Country: Australia
Phone: +61 3 9288 4020
Fax: +61 3 9416 0926
Email: knightkr@svhm.org.au
© 2004
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