Fibrillar extracellular matrix produced by pericyte-like cells facilitates glioma cell dissemination
Author
Vepřková, Jana
Vodicka, Petr
Tomas, Robert
Publication date
2024Published in
Brain PathologyVolume / Issue
34 (6)ISBN / ISSN
ISSN: 1015-6305ISBN / ISSN
eISSN: 1750-3639Metadata
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This publication has a published version with DOI 10.1111/bpa.13265
Abstract
Gliomagenesis induces profound changes in the composition of the extracellular matrix (ECM) of the brain. In this study, we identified a cellular population responsible for the increased deposition of collagen I and fibronectin in glioblastoma. Elevated levels of the fibrillar proteins collagen I and fibronectin were associated with the expression of fibroblast activation protein (FAP), which is predominantly found in pericyte-like cells in glioblastoma. FAP+ pericyte-like cells were present in regions rich in collagen I and fibronectin in biopsy material and produced substantially more collagen I and fibronectin in vitro compared to other cell types found in the GBM microenvironment. Using mass spectrometry, we demonstrated that 3D matrices produced by FAP+ pericyte-like cells are rich in collagen I and fibronectin and contain several basement membrane proteins. This expression pattern differed markedly from glioma cells. Finally, we have shown that ECM produced by FAP+ pericyte-like cells enhances the migration of glioma cells including glioma stem-like cells, promotes their adhesion, and activates focal adhesion kinase (FAK) signaling. Taken together, our findings establish FAP+ pericyte-like cells as crucial producers of a complex ECM rich in collagen I and fibronectin, facilitating the dissemination of glioma cells through FAK activation. FAP+ pericyte-like cells drive the deposition of fibrillar extracellular matrix proteins such as collagen I and fibronectin in glioblastoma, facilitating glioma cell dissemination and activation of focal adhesion kinase. image
Keywords
collagen type I, extracellular matrix proteins, fibronectin, glioblastoma, pericytes, proteomics,
Permanent link
https://hdl.handle.net/20.500.14178/2513License
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