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Cellular responses of murine epiphyseal cartilage to mechanical injury

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Title: Cellular responses of murine epiphyseal cartilage to mechanical injury
Authors: Chong, Ka-Wing
Item Type: Thesis or dissertation
Abstract: Our laboratory has defined a rapid cellular response in porcine articular cartilage to injury. To enable study of the injury response in genetically modified animals I have characterized a novel model of cartilage injury in the mouse, involving avulsion of femoral head epiphyseal cartilage from 4-6 week old animals, and maintaining the explanted tissue in culture. Avulsion injury (explantation) of murine cartilage rapidly activated mitogen activated protein kinases (MAPKs) and nuclear factor κB (NFκB), thus establishing a close similarity to porcine tissue. Gene expression (mRNA) was analysed on Taqman® Low density array microfluidic cards for 47 pre-selected genes. 25 were upregulated upon injury; many characteristic of the inflammatory response. Some were upregulated early (by 1 h) and some not till after 4 h, suggesting primary and secondary responses. Re-cutting cartilage adapted to culture only activated a subset of genes, probably due to release of fibroblast growth factor 2 (FGF2) which is stored pericellularly. Gene expression profiling of explanted cartilage of Fgf2-deficient mice showed 7 of the 25 (28%) genes were partly or largely FGF2-dependent. Because the gene and signalling profiles resembled an inflammatory response I examined tissue deficient in the myeloid differentiation 88 protein (MyD88) an adaptor protein for signalling of the interleukin-1 receptor and toll-like receptor family. 12 of the 25 genes were MyD88-dependent. MyD88-/- cartilage did not show impairment of the intracellular signalling response upon injury and expression of a MyD88-dependent gene (Ccl2) did not increase till 4 h of culture. It was likely that a MyD88-using ligand was made during the primary response and contributed to the secondary. I conclude there are at least 3 mechanisms by which cartilage injury activates gene expression: 1) release of pericellular FGF2, 2) an unkown trigger of MAPK and NFκB and 3) secondary production of a MyD88-using factor.
Issue Date: Sep-2011
Date Awarded: Mar-2012
URI: http://hdl.handle.net/10044/1/9487
DOI: https://doi.org/10.25560/9487
Supervisor: Vincent, Tonia
Saklatvala, Jeremy
Department: Medicine: Kennedy Institute of Rheumatology
Publisher: Imperial College London
Qualification Level: Doctoral
Qualification Name: Doctor of Philosophy (PhD)
Appears in Collections:Medicine PhD theses



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