Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro

Dissertation (MSc (Pharmacology))--University of Pretoria, 2023.

Saved in:
Bibliographic Details
Other Authors: Flepisi, Brian
Format: Thesis
Language:English
Published: University of Pretoria 2023
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613527502487552
access_status_str Open Access
author2 Flepisi, Brian
author_browse Flepisi, Brian
author_facet Flepisi, Brian
collection Thesis
dc_rights_str_mv © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Pharmacology))--University of Pretoria, 2023.
format Thesis
id oai:repository.up.ac.za:2263/93831
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:37:34.018Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2023
publishDateRange 2023
publishDateSort 2023
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/93831 Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro Flepisi, Brian xolisilemokoena@gmail.com Cordier, Werner Mabeta, Peace Mokoena, Xolisile UCTD Blood-brain barrier Endothelial cells Glioblastoma Secretome Conditioned media Co-culture Dissertation (MSc (Pharmacology))--University of Pretoria, 2023. Introduction: Invasion of cancer cells within the central nervous system (CNS) can impact the blood-brain barrier (BBB) directly through cell invasion or indirectly through the cancer secretome. The BBB, formed mainly by endothelial cells, is a crucial protective barrier of the CNS. Glioblastoma (GBM) is the most aggressive and malignant tumour of the CNS, with high mortality and an average survival rate of 12 to 15 months with treatment. The underlying mechanisms of BBB disruption due to GBM remain unclear. To elucidate the overall effect GBM has on the BBB, this study aimed to investigate the effect of GBM-conditioned media and cells on endothelial cell growth, migration, permeability, and the expression of tight junctions. Methods: The brain endothelial cell line (bEnd.3) was used as a model of the BBB. The GBM (U87) cell line was used to collect conditioned media (CM) at 48 hours (h) and for the indirect co-culture with End.3 cells. The study used two endothelial models: mono-culture of bEnd.3 cells treated with U87-CM and an indirect co-culture of bEnd.3 cells with U87 cells. Both models were compared to a mono-culture of bEnd.3 cells untreated (negative control). The endothelial cell morphology (by phase-contrast microscopy), and the cytotoxicity of CM (using the sulforhodamine B assay), were assessed on the untreated bEnd.3 mono-culture and CM treated mono-culture of bEnd.3 cells. The following was conducted in the two models: endothelial cell migration rate (scratch migration assay), cell growth (xCELLigence real-time cell analyser system), barrier integrity (sodium fluorescein permeability), and tight junction protein expression (Western blotting). Results: The cytotoxic effects of CM on bEnd.3 cells were observed only in the U87-CM collected at 96 h. The U87-CM suppressed the growth of bEnd.3 cells. Conversely the indirect co-culture significantly increased cell growth (p<0.05). The U87-CM increased the migration of bEnd.3 cells from 10% at 24 h to 33% at 48 h compared to the negative control. The U87-CM did not alter permeability of bEnd.3 cells, whereas the indirect co-culture weakened the permeability of the barrier from 15.97 × 10-5 cm/s (negative control) to 20.96 × 10-5 cm/s (treated bEnd.3 cells). The U87-CM increased the expression levels of occludin and ZO-1 in bEnd.3 cells following 48 h, compared to the negative control. The indirect co-culture increased the expression of ZO-1 by 1.2 fold following 48 h exposure. Conclusion: The chosen U87-CM did not alter the morphology of endothelial cells and had minimal cytotoxic effect on the bEnd.3 cells. However, a real-time analysis of the bEnd.3 cell growth revealed that U87-CM suppressed cell growth, and an indirect co-culture with the U87 cells promoted cell growth. The CM maintained the integrity of the BBB and the co-culture caused BBB instability. Both U87-CM and U87 indirect co-culture can influence the growth, migration, permeability, and tight junction expression process in bEnd.3 cells. It is evident that the secreted factors play a role in BBB modulation. However, further investigations are required to understand the signalling pathways activated by the secretome in CM and indirect co-culture on bEnd.3 cells. Pharmacology MSc (Pharmacology) Unrestricted Faculty of Health Sciences None 2023-12-20T06:35:44Z 2023-12-20T06:35:44Z 2024-04 2023 Dissertation * A2024 http://hdl.handle.net/2263/93831 en © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Blood-brain barrier
Endothelial cells
Glioblastoma
Secretome
Conditioned media
Co-culture
Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title_full Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title_fullStr Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title_full_unstemmed Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title_short Effect of glioblastoma cells on brain endothelial cell growth, migration, permeability, and tight junction proteins in vitro
title_sort effect of glioblastoma cells on brain endothelial cell growth migration permeability and tight junction proteins in vitro
topic UCTD
Blood-brain barrier
Endothelial cells
Glioblastoma
Secretome
Conditioned media
Co-culture
url http://hdl.handle.net/2263/93831