Investigating the Interactions of Glioma Stem Cells in the Perivascular Niche at Single-Cell Resolution using a Microfluidic Tumor Microenvironment Model

被引:32
作者
Adjei-Sowah, Emmanuela A. [1 ]
O'Connor, Samantha A. [1 ]
Veldhuizen, Jaimeson [1 ]
Lo Cascio, Costanza [2 ]
Plaisier, Christopher [1 ]
Mehta, Shwetal [2 ]
Nikkhah, Mehdi [1 ,3 ]
机构
[1] Arizona State Univ, Sch Biol & Hlth Syst Engn, Tempe, AZ 85287 USA
[2] St Josephs Hosp, Ivy Brain Tumor Ctr, Barrow Neurol Inst, 350 Thomas Rd, Phoenix, AZ 85013 USA
[3] Arizona State, Virginia G Piper Biodesign Ctr Personalized Diagn, Tempe, AZ 85287 USA
基金
美国国家科学基金会;
关键词
glioblastoma; invasion; perivascular niche; transcriptomics; tumor microenvironment; FORMYLPEPTIDE RECEPTOR; GENOMIC ANALYSIS; LGR6; PROMOTES; IN-VITRO; GLIOBLASTOMA; INVASION; PROLIFERATION; CANCER; PDGFRA; TEMOZOLOMIDE;
D O I
10.1002/advs.202201436
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
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页数:16
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