Cambareri, Antony Charles2006-12-282006-12-2820042004http://hdl.handle.net/2440/22172"October 2004"Includes bibliographical references (leaves 201-256)xiv, 256 leaves, [9] p. : ill., plates (col.) ; 30 cm.c-Kit is a member of the Receptor Tyrosine Kinase Type III family and has four naturally occurring isoforms. The work presented in chapter 3 utilised full-length human or murine c-Kit cDNA expressed in murine cells. Over-expression of normal c-Kit was capable of contributing to oncogenic transformation. The analysis of human c-Kit isoforms demonstrated dissociation of various indicators of transformation (anchorage independence, loss of contact inhibition, tumourigenicity) in the NIH3T3 cell model. Biochemical analysis of the c-Kit signalling revealed qualitative and quantitative differences between the GNNK+ and GNNK- c-Kit isoforms. The GNNK- isoform was hyperphosphorylated more extensively and rapidly, and was also more efficiently ubiquitinated and degraded than the GNNK+ counterpart. PI3-K was recruited and activated equally by both isoforms. Phosphorylation of MAPK paralleled that of the c-Kit isoform's phosphorylation. In Chapter 4, a new model was developed using a chimaeric human extracellular c-Kit/murine transmembrane+ intracellular c-Kit. This new molecule in conjunction with a murine Myb Immortalised Haemopoietic Cell (MIHC) line was used to investigate a number of biological outcomes stimulated by scF simultaneously. A MIHC line lacking Lyn was also analysed. Chimaeric c-Kit displayed the same signalling characteristics exhibited by its' full-length human counterpart. The model showed that the GNNK- isoform was superior in its survival stimulus to GNNK+, but both were equivalent in promoting proliferation. The absence of Lyn reduced the ability of both isoforms to promote survival. The aim of work in Chapter 5 was to elucidate the expression patterns of the c-Kit isoforms in subsets of normal human haemopoietic cells. Methodology was developed to detect GNNK+/- c-Kit mRNA from rare subsets of cells from bone marrow. As c-Kit is known to be down-modulated in mobilised peripheral blood stem cells, mobilised CD34+ cells were also investigated. In all haemopoietic cells analysed, there was no significant difference in expression patterns of the c-Kit isoforms, with all samples expressing approximately 90% of total c-Kit transcripts as the GNNK- isoform. c-Kit downmodulation observed in mobilisation of CD34+ cells was not influenced at the level of transcription, but at the protein level.85669 bytesapplication/pdfenProtein-tyrosine kinase.Cell metabolismThesis