https://www.um.edu.mt/library/oar/handle/123456789/64209 2026-04-27T23:58:18Z 2026-04-27T23:58:18Z https://www.um.edu.mt/library/oar/handle/123456789/31721 2020-11-19T16:08:05Z 2006-01-01T00:00:00Z

Title: The HIF system and Inhibitory PAS Domain Protein (IPAS) - a role in vascular remodelling Abstract: In mammalian cells, the hypoxic response is mediated by a family of transcription factors known as hypoxia inducible factors (HI F). These are heterodimers composed of a tightly regulated alpha subunit and a constituitively expressed beta subunit (also known as aryl hydrocarbon nuclear translocator, ARNT). Three 0.- subunits have been identified so far, HIF-1 α, HIF-2 α and HIF-3 α. HIF-1 α and HIF-2 α are regulated mostly At the protein level via oxygen depedent degredation by the proteasome. Hypoxia leads to their stabilisation, binding to hypoxia responsive elements (HRE) and target gene transactivation. HIF-3 α is still poorly characterised. In mouse, a HIF- 3 α splice variant called inhibitory PAS domain protein has an inhibitory effect on HIF- 10. mediated activity. In humans a number of HII--3a splice variants have been reported. It was one aim of this study to investigate the roles of the largest isoform, HIF-3a1, and a smaller isoform resembling mouse IPAS, HIF-3a3, in the hypoxic response of endothelial cells. Both variants were expressed in vascular cells and in the vascular wall. HIF-3 α 1 but not HIF-3a3 was regulated by tile proteasome. Whilst both proteins were found to interact with HIF-1a and ARNT, HIF-3a1 was found to bind to the HRE and disturb HIF-1 α -DNA binding. A competition mechanism between HIF-3 α isoforms and HIF-1 α was found to cause downregulation of HIF-1 transcriptional activity resulting in decreased endothelial cell proliferation and angiogenesis under hypoxia. The second part of the study aimed to clarify the mechanism by which non-hypoxic stimuli can upregulate HIF-1a in pulmonary artery smooth muscle cells. HIF-1a upregulation by thrombin occurred via an ROS dependent mechanism by activation of the NADPH oxidase. This led to upregulation of NFKB activity which interacted with a novel binding site on the HIF-1a promoter and induced its transcription. Description: PH.D.

2006-01-01T00:00:00Z