Fibrillar extracellular matrix produced by pericyte-like cells facilitates glioma cell dissemination
Autor
Vepřková, Jana
Vodicka, Petr
Tomas, Robert
Datum vydání
2024Publikováno v
Brain PathologyRočník / Číslo vydání
34 (6)ISBN / ISSN
ISSN: 1015-6305ISBN / ISSN
eISSN: 1750-3639Metadata
Zobrazit celý záznamKolekce
Tato publikace má vydavatelskou verzi s DOI 10.1111/bpa.13265
Abstrakt
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
Klíčová slova
collagen type I, extracellular matrix proteins, fibronectin, glioblastoma, pericytes, proteomics,
Trvalý odkaz
https://hdl.handle.net/20.500.14178/2513Licence
Licence pro užití plného textu výsledku: Creative Commons Uveďte původ 4.0 International