Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/123507
Type: Thesis
Title: Osteochondroreticular stem cell therapy for osteoarthritis: the right cells for the job
Author: Ng, Jia Qi
Issue Date: 2019
School/Discipline: Adelaide Medical School
Abstract: Osteoarthritis (OA) is a disease of synovial joints characterized by clinical symptoms and pathology related to the whole joint including the periarticular tissues such as the muscles, ligaments and bone. Central to the pathogenesis and diagnosis, however, is the degeneration of articular cartilage. Current treatments include lifestyle modification to prevent further injury, analgesic drugs to help reduce symptoms and surgical interventions such as joint replacement. More recently stem cell therapies, either stimulating endogenous populations or infusing new cells, have been investigated. While OA is a multifactorial disorder, as a foundation to stem cell therapeutics one must accept the premise that OA pathogenesis, at least in part, is contributed to by stem cell dysfunction. Perhaps, a relative insufficiency of developmental articular chondrogenesis, inadequate replenishment during adult homeostasis or incomplete repair following mechanical and inflammatory challenges to cartilaginous integrity such as injury, obesity and ageing. Following the discovery of skeletal stem cells marked by the expression of Gremlin 1 (Grem1) being shown to give rise to chondrocytes in vivo, we studied transgenic mice to trace the Grem1-expressing cells in comparison to other MSC populations marked by the expression of Leptin receptor (LepR) and a common chondrocyte marker Aggrecan (Acan) in the knee articular cartilage. We found that Grem1-expressing cells label a stem cell population within the mouse knee articular cartilage in development as well as in adulthood. We then used a mouse model of OA, destabilisation of the medial meniscotibial (DMM) surgery, in these transgenic mice to test how injury modulates this population. We evaluated the single cell expression of these cells in the knee articular cartilage, by scRNASeq and generated a new mouse line to allow easy ablation of the Grem1 expressing cells within the knee articular cartilage. We also expanded these cells in vitro both to study their relative in vitro characteristics, as well as for injection back into our OA disease model. This thesis presents a comprehensive re-evaluation of articular stem cell biology and applies it to the important and increasingly global clinical problem of osteoarthritis. This work has made new discoveries, generated new transgenic mouse reagents and has stimulated ongoing translational research to better understand osteoarthritis and develop new approaches to its prevention and treatment.
Advisor: Haynes, David
Worthley, Daniel
Menicanin, Danijela
Dissertation Note: Thesis (Ph.D.) -- University of Adelaide, Adelaide Medical School, 2020
Keywords: Stem cells
osteoarthritis
Provenance: This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
Appears in Collections:Research Theses

Files in This Item:
File Description SizeFormat 
Ng2019_PhD.pdf6.33 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.