TY - JOUR
T1 - Investigating the Interactions of Glioma Stem Cells in the Perivascular Niche at Single-Cell Resolution using a Microfluidic Tumor Microenvironment Model
AU - Adjei-Sowah, Emmanuela A.
AU - O'Connor, Samantha A.
AU - Veldhuizen, Jaimeson
AU - Lo Cascio, Costanza
AU - Plaisier, Christopher
AU - Mehta, Shwetal
AU - Nikkhah, Mehdi
N1 - Funding Information:
E.A.A.‐S., S.A.O., and J.V. contributed equally to this work. This work was supported by NSF Award # 1914680, NIH‐NINDS Award # 1R01NS123038‐01, and 1R01NS119650‐01 (CLP). The authors also acknowledge Nicholas Mellor and Joy Blain for their assistance in scRNA‐seq isolation. Schematics were made in Biorender.com.
Funding Information:
E.A.A.-S., S.A.O., and J.V. contributed equally to this work. This work was supported by NSF Award # 1914680, NIH-NINDS Award # 1R01NS123038-01, and 1R01NS119650-01 (CLP). The authors also acknowledge Nicholas Mellor and Joy Blain for their assistance in scRNA-seq isolation. Schematics were made in Biorender.com.
Publisher Copyright:
© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.
PY - 2022/7/25
Y1 - 2022/7/25
N2 - The perivascular niche (PVN) is a glioblastoma tumor microenvironment (TME) that serves as a safe haven for glioma stem cells (GSCs), and acts as a reservoir that inevitably leads to tumor recurrence. Understanding cellular interactions in the PVN that drive GSC treatment resistance and stemness is crucial to develop lasting therapies for glioblastoma. The limitations of in vivo models and in vitro assays have led to critical knowledge gaps regarding the influence of various cell types in the PVN on GSCs behavior. This study developed an organotypic triculture microfluidic model as a means to recapitulate the PVN and study its impact on GSCs. This triculture platform, comprised of endothelial cells (ECs), astrocytes, and GSCs, is used to investigate GSC invasion, proliferation and stemness. Both ECs and astrocytes significantly increased invasiveness of GSCs. This study futher identified 15 ligand-receptor pairs using single-cell RNAseq with putative chemotactic mechanisms of GSCs, where the receptor is up-regulated in GSCs and the diffusible ligand is expressed in either astrocytes or ECs. Notably, the ligand–receptor pair SAA1-FPR1 is demonstrated to be involved in chemotactic invasion of GSCs toward PVN. The novel triculture platform presented herein can be used for therapeutic development and discovery of molecular mechanisms driving GSC biology.
AB - The perivascular niche (PVN) is a glioblastoma tumor microenvironment (TME) that serves as a safe haven for glioma stem cells (GSCs), and acts as a reservoir that inevitably leads to tumor recurrence. Understanding cellular interactions in the PVN that drive GSC treatment resistance and stemness is crucial to develop lasting therapies for glioblastoma. The limitations of in vivo models and in vitro assays have led to critical knowledge gaps regarding the influence of various cell types in the PVN on GSCs behavior. This study developed an organotypic triculture microfluidic model as a means to recapitulate the PVN and study its impact on GSCs. This triculture platform, comprised of endothelial cells (ECs), astrocytes, and GSCs, is used to investigate GSC invasion, proliferation and stemness. Both ECs and astrocytes significantly increased invasiveness of GSCs. This study futher identified 15 ligand-receptor pairs using single-cell RNAseq with putative chemotactic mechanisms of GSCs, where the receptor is up-regulated in GSCs and the diffusible ligand is expressed in either astrocytes or ECs. Notably, the ligand–receptor pair SAA1-FPR1 is demonstrated to be involved in chemotactic invasion of GSCs toward PVN. The novel triculture platform presented herein can be used for therapeutic development and discovery of molecular mechanisms driving GSC biology.
KW - glioblastoma
KW - invasion
KW - perivascular niche
KW - transcriptomics
KW - tumor microenvironment
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U2 - 10.1002/advs.202201436
DO - 10.1002/advs.202201436
M3 - Article
C2 - 35619544
AN - SCOPUS:85130595082
SN - 2198-3844
VL - 9
JO - Advanced Science
JF - Advanced Science
IS - 21
M1 - 2201436
ER -