Luiz Fernando Cardoso Garcia,
Scientist,
Biociências e Biotecnologia do Instituto Carlos Chagas
Bachelor in Veterinary Medicine by Pontifícia Universidade Católica do Paraná (2013-2018) with academic distinction award. Masters degree in Bioscience and Biotechnology by Programa de Pós-Graduação em Biociências e Biotecnologia do Instituto Carlos Chagas-FIOCRUZ/PR (2018-2020). Doctoral student in Bioscience and Biotechnology in the same institution. Member of the research group in Apicomplexa in ICC-FIOCRUZ/PR. Work with the following subjects: host/pathogen interaction; infectious context immunology; extracellular vesicles; endothelial cells.
Temporal Influence of Extracellular Vesicle-Depleted Serum on Extracellular Vesicles and Endothelial Cells
Tuesday, 25 June 2024 at 18:00
Add to Calendar ▼2024-06-25 18:00:002024-06-25 19:00:00Europe/LondonTemporal Influence of Extracellular Vesicle-Depleted Serum on Extracellular Vesicles and Endothelial CellsPoint-of-Care, Biosensors and Rapid Dx Europe 2024 in Rotterdam, The NetherlandsRotterdam, The NetherlandsSELECTBIOenquiries@selectbiosciences.com
Extracellular vesicles (EVs) are generated by various cell types, including endothelial cells. The presence of EVs in fetal bovine serum (FBS), commonly used in cell culture, has been recognized as a potential confounding factor. To elucidate this, human brain microvascular endothelial cells (HBMEC) were cultured for 2 or 24 hours in the presence of EV-depleted FBS (EVdS). Cell viability, gene and protein expression, and EVs isolated from these cells were assessed. Additionally, EV uptake, ICAM-1 expression, and monocyte adhesion to HBMEC exposed to EVs were also examined. Elevated apoptosis rates in cells cultured with EVdS for 2 and 24 hours was observed. Within 2 hours, there was an upregulation of IL8, followed by the downregulation of IL6 and IL8 after 24 hours. Proteomic analysis revealed that EVs cultured for 2 hours (EV2h) were enriched in proteins associated with ribosomes and carbon metabolism, while those cultured for 24 hours (EV24h) exhibited proteins linked to cell adhesion and platelet activation. Moreover, HBMECs exposed to EV2h displayed increased ICAM-1 expression and monocyte adhesion compared to cells exposed to EV24h. These findings highlight that HBMECs cultured with EVdS produce EVs with distinct physical characteristics and protein content that varies across time.
Add to Calendar ▼2024-06-24 00:00:002024-06-25 00:00:00Europe/LondonPoint-of-Care, Biosensors and Rapid Dx Europe 2024Point-of-Care, Biosensors and Rapid Dx Europe 2024 in Rotterdam, The NetherlandsRotterdam, The NetherlandsSELECTBIOenquiries@selectbiosciences.com