Author:
Jain Saket,Rick Jonathan W.,Joshi Rushikesh,Beniwal Angad,Spatz Jordan,Chang Alexander Chih-Chieh,Nguyen Alan T.,Sudhir Sweta,Chandra Ankush,Haddad Alex,Wadhwa Harsh,Shah Sumedh S.,Choi Serah,Hayes Josie L.,Wang Lin,Yagnik Garima,Costello Joseph F.,Diaz Aaron,Aghi Manish K.
Abstract
ABSTRACTDespite their identification in some cancers, pro-tumoral cancer-associated fibroblasts (CAFs) were presumed absent in glioblastoma given the lack of brain fibroblasts. Serial trypsinization of primary glioblastoma cultures yielded cells with CAF morphology, CAF transcriptomic profile, and mesenchymal lineage in single-cell RNA-seq. Glioblastoma CAFs were attracted to glioblastoma stem cells (GSCs) and CAFs enriched GSCs. We created a resource of inferred crosstalk by mapping expression of receptors to their cognate ligands, identifying PDGF-β and TGF-β as mediators of GSC effects on CAFs, and osteopontin and hepatocyte growth factor as mediators of CAF-induced GSC enrichment. Glioblastoma CAFs also induced M2 macrophage polarization by producing the EDA fibronectin variant. Glioblastoma CAFs were enriched in the subventricular zone which houses neural stem cells that produce GSCs. Including CAFs in GSC-derived xenografts induced in vivo growth. These findings are among the first to identify glioblastoma CAFs and their GSC interactions, making them an intriguing target.
Publisher
Cold Spring Harbor Laboratory
Cited by
5 articles.
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