Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Permanent URI for this collectionhttps://hdl.handle.net/11147/9
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Book Structural Defense of Plants and Pathogenesis(01. Izmir Institute of Technology, 2023) Ekinci, Berkay; Ekinci, BerkayThe major challenge in today s world is ensuring an adequate food supply for the growing global population. Achieving this goal requires the development of crops by using sustainable agricultural strategies in ecologically suitable areas (Jan et al. 2011; Doğanlar et al. 2023). However, plant diseases, which are caused by various pathogens such as bacteria, fungi, viruses, nematodes, and herbivores, pose a significant threat to crop quality and yield. Fortunately, plants have several preexisting and induced defense and immune mechanisms to protect themselves against biotic and abiotic stresses (Jones et al. 2006; Freeman et al. 2008). This review aims to provide information on phytopathogens, the steps of pathogenesis, plants’ pre-existing structural defense mechanisms against pathogenesis, and more. It is aimed at broadening the reader's knowledge and perspective by providing a wide range of examples, from simple to complex. I hope that this review will be a good start for enlightening and inspiring all curious scientists who, like me, are enthusiastic about this field.Master Thesis Investigation of the Pathology of Brain Derived Endothelial Cells in In-Vitro Hypoxia Models(01. Izmir Institute of Technology, 2021) Erdemli, Kısmet Tuğçe; Tosun, ÇiğdemThe blood brain barrier (BBB) is a vital structure that protects brain homeostasis. Endothelial cells (EC) have a significant role in regulating the BBB structure and function. Several studies have revealed the association of SUR1-TRPM4 channels that regulate this secondary damage of CNS injuries. After the activation of the channel, Na+ influx causes depolarization, cell swelling (edema) and ultimately oncotic cell death. Hypoxia inducing factor (HIF) transcription factor that has been reported to activate more than 100 genes to adapt to a hypoxic condition. Once Hif1-⍺ is translocated into the nucleus, it can dimerize with HIF1-ß to produce HIF that is critical in hypoxic conditions and regulate cell cycle arrest or cell death pathways. Hypoxia can occur in an O2 dependent and independent manner. In this study, CoCl2 and hypoxia chamber which was cost-effective and reliable were optimized. Cellular death was calculated with Trypan blue staining in this novel hypoxia chamber model and compared with CoCl2 models. In addition, morphological changes were observed in microscopic analysis. Hif1-⍺, caspase-3 and NF-κB translocation to the nucleus localization were quantified. Cell viability was different between the CoCl2 model and novel hypoxia chamber model at 24 hours. The cellular death increased with CoCl2 exposure, where no change was noted in the hypoxia chamber model. Time dependent Hif1-⍺ upregulation was also demonstrated that peaked at 12-hours. Finally, NF-κB translocation into the nucleus was significantly increased at 24 hours of hypoxia exposure. The results reveal that the inflatable hypoxia chamber model could be reliably used to mimic hypoxia in an in-vitro setting. Hif1-⍺ activated in a time dependent manner, along with NF-κB. The upregulation of these transcription factors can ultimately affect the cellular death mechanisms differently