E-Thesis 177 views
Molecular and Cellular Analysis of Endothelial Permeability in Sepsis / YUEXI GUO
Swansea University Author: YUEXI GUO
DOI (Published version): 10.23889/SUthesis.66391
Abstract
Sepsis is a common manifestation of multidrug-resistant (MDR) bacterial infections. Lipopolysaccharide (LPS), a bacterial membrane component, in sepsis is responsible for vascular endothelial barrier dysfunction. Thrombin plays a key role in sepsis, which causes increased endothelial cell (EC) perme...
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Swansea, Wales, UK
2024
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| Institution: | Swansea University |
| Degree level: | Doctoral |
| Degree name: | Ph.D |
| Supervisor: | Kanamarlapudi, Venkateswarlu ; Wilkinson, Thomas |
| URI: | https://cronfa.swan.ac.uk/Record/cronfa66391 |
| Abstract: |
Sepsis is a common manifestation of multidrug-resistant (MDR) bacterial infections. Lipopolysaccharide (LPS), a bacterial membrane component, in sepsis is responsible for vascular endothelial barrier dysfunction. Thrombin plays a key role in sepsis, which causes increased endothelial cell (EC) permeability and von Willebrand factor (vWF) secretion. Coronavirus disease (COVID)-19, which is caused by severe acute respiratory syndrome coronavirus (SARS CoV)-2, is a ‘vascular disease’ and it can also result in sepsis, which causes epithelial and endothelial barrier dysfunction and increases the secretion of von Willebrand factor (vWF) and zonulin. ADP-ribosylation factor (ARF)1 and ARF6 are potentially involved in LPS-, thrombin- or SARS-CoV-2 spike protein S1 receptor binding domain (RBD)-triggered-cellular response. In this study, we first analysed in vitro how LPS, thrombin and the RBD induce EC permeability and ARF1/6 activation by standardising a novel trans-monolayer permeability assay to assess the permeability of EA.hy 926 endothelial cells and the GST-Golgi-localised, gamma-ear-containing, ARF-binding protein (GGA)3 protein-binding domain (PBD) pull-down assay to evaluate the ARF activation, respectively. Secondly, we evaluated the secretion levels of cytokines [tumour necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1β] or vWF in the LPS-, thrombin- or SARS-CoV-2 spike protein-treated EA.hy 926 cells. Thirdly, we analysed the downstream signalling cascade responsible for LPS- or thrombin-induced EC permeability and/or vWF secretion and the underlying mechanism response to the RBD-induced EC permeability and vWF secretion or epithelial cell permeability and zonulin secretion by using the inhibitory peptides and chemical inhibitors. In conclusion, we showed that LPS, thrombin and the RBD are sufficient to induce EC permeability and ARF1/6 activation but not cytokine secretion. We also showed that thrombin and the RBD markedly induce vWF secretion. However, we found that thrombin induces EC permeability rapidly and reversibly, which is different from the secretion of vWF levels induced by thrombin. In addition, we dissected the MyD88/cytohesin 2/ARF6 signalling cascade downstream of toll-like receptor (TLR)4 for LPS-induced EC permeability. We also found that Rac1 plays a role in the cAMP inhibition of EC permeability induced by thrombin. Moreover, we showed that the RBD induces EC permeability and vWF secretion through the angiotensin-converting enzyme (ACE)2 receptor in an ARF6 activation-dependent manner. However, the mutants, including those in South African and South Californian variants of SARS-CoV-2, of the spike protein didn’t affect its induction of EC permeability or vWF secretion. We also identified a signalling cascade downstream of angiotensin-converting enzyme (ACE)2 for SARS CoV-2 spike protein-induced EC permeability and its vWF secretion, using pharmacological inhibitors. The RBD induced epithelial permeability and zonulin secretion but at negligible levels. However, the RBD altered neither ACE2 expression nor ARF6 activation in epithelial cells. Additionally, the inhibitors, which were used for identifying the signalling cascade downstream for the EC permeability and its vWF secretion induced by the RBD, did not affect the RBD-induced epithelial permeability or its zonulin secretion. However, a better epithelial model cell line is required to study epithelial cell permeability and zonulin secretion. The knowledge gained from this study could be useful in developing novel drugs or repurposing existing drugs for treating Sepsis and COVID-19. |
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| Keywords: |
Sepsis, COVID-19 and endothelial/epithelial vascular permeability |
| College: |
Faculty of Medicine, Health and Life Sciences |