Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes

<b>Background/Objectives</b>: Brain cancers offer poor prognoses to patients accompanied by symptoms that drastically impact the patient and their family. Brain tumours recruit local non-transformed cells to provide trophic support and immunosuppression within the tumour microenvironment...

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Main Authors: Samuel McCullough, Eliene Albers, Akshata Anchan, Jane Yu, Bronwen Connor, E. Scott Graham
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Onco
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Online Access:https://www.mdpi.com/2673-7523/4/4/27
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author Samuel McCullough
Eliene Albers
Akshata Anchan
Jane Yu
Bronwen Connor
E. Scott Graham
author_facet Samuel McCullough
Eliene Albers
Akshata Anchan
Jane Yu
Bronwen Connor
E. Scott Graham
author_sort Samuel McCullough
collection DOAJ
description <b>Background/Objectives</b>: Brain cancers offer poor prognoses to patients accompanied by symptoms that drastically impact the patient and their family. Brain tumours recruit local non-transformed cells to provide trophic support and immunosuppression within the tumour microenvironment, supporting tumour progression. Given the localisation and supportive role of pericytes at the brain vasculature, we explored the potential for brain pericytes to contribute to the brain cancer microenvironment. <b>Methods</b>: To investigate this, primary brain pericytes were treated with factors commonly upregulated in brain cancers. Immunofluorescent labelling identified changes to brain pericyte cell signalling, cytometric bead array measured inflammatory secretion, and flow cytometry investigated brain pericyte phagocytosis. <b>Results</b>: The TGFβ superfamily cytokines TGFβ and GDF-15 activated SMAD2/3 and inhibited C/EBP-δ, revealing a potential mechanism behind the pleiotropic action of TGFβ on brain pericytes. IL-17 induced secretion of IL-6 without activating NFκB, STAT1, SMAD2/3, or C/EBP-δ signalling pathways. IL-27 and IFNγ induced STAT1 signalling and significantly reduced brain pericyte phagocytosis. The remaining brain cancer-derived factors did not induce a measured response, indicating that these factors may act on other cell types or require co-stimulation with other factors to produce significant effects. <b>Conclusions</b>: We identify several brain cancer-secreted factors which alter relevant brain pericyte functions. This reveals mechanisms through which brain tumours may regulate brain pericyte activity and these data start to uncover the supportive role these cells may play in brain cancers.
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spelling doaj-art-d9db3e3847f64cd99e026be3039ab3dd2025-08-20T02:57:28ZengMDPI AGOnco2673-75232024-11-014438139610.3390/onco4040027Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain PericytesSamuel McCullough0Eliene Albers1Akshata Anchan2Jane Yu3Bronwen Connor4E. Scott Graham5Department of Anatomy and Medical Imaging, University of Auckland, Auckland 1023, New ZealandDepartment of Anatomy and Medical Imaging, University of Auckland, Auckland 1023, New ZealandCentre for Brain Research, University of Auckland, Auckland 1023, New ZealandCentre for Brain Research, University of Auckland, Auckland 1023, New ZealandCentre for Brain Research, University of Auckland, Auckland 1023, New ZealandCentre for Brain Research, University of Auckland, Auckland 1023, New Zealand<b>Background/Objectives</b>: Brain cancers offer poor prognoses to patients accompanied by symptoms that drastically impact the patient and their family. Brain tumours recruit local non-transformed cells to provide trophic support and immunosuppression within the tumour microenvironment, supporting tumour progression. Given the localisation and supportive role of pericytes at the brain vasculature, we explored the potential for brain pericytes to contribute to the brain cancer microenvironment. <b>Methods</b>: To investigate this, primary brain pericytes were treated with factors commonly upregulated in brain cancers. Immunofluorescent labelling identified changes to brain pericyte cell signalling, cytometric bead array measured inflammatory secretion, and flow cytometry investigated brain pericyte phagocytosis. <b>Results</b>: The TGFβ superfamily cytokines TGFβ and GDF-15 activated SMAD2/3 and inhibited C/EBP-δ, revealing a potential mechanism behind the pleiotropic action of TGFβ on brain pericytes. IL-17 induced secretion of IL-6 without activating NFκB, STAT1, SMAD2/3, or C/EBP-δ signalling pathways. IL-27 and IFNγ induced STAT1 signalling and significantly reduced brain pericyte phagocytosis. The remaining brain cancer-derived factors did not induce a measured response, indicating that these factors may act on other cell types or require co-stimulation with other factors to produce significant effects. <b>Conclusions</b>: We identify several brain cancer-secreted factors which alter relevant brain pericyte functions. This reveals mechanisms through which brain tumours may regulate brain pericyte activity and these data start to uncover the supportive role these cells may play in brain cancers.https://www.mdpi.com/2673-7523/4/4/27brain pericyteneuroinflammationcytokine screeningphagocytosiscell signallingglioblastoma
spellingShingle Samuel McCullough
Eliene Albers
Akshata Anchan
Jane Yu
Bronwen Connor
E. Scott Graham
Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
Onco
brain pericyte
neuroinflammation
cytokine screening
phagocytosis
cell signalling
glioblastoma
title Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
title_full Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
title_fullStr Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
title_full_unstemmed Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
title_short Screening Activity of Brain Cancer-Derived Factors on Primary Human Brain Pericytes
title_sort screening activity of brain cancer derived factors on primary human brain pericytes
topic brain pericyte
neuroinflammation
cytokine screening
phagocytosis
cell signalling
glioblastoma
url https://www.mdpi.com/2673-7523/4/4/27
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