Fibrillar extracellular matrix produced by pericyte-like cells facilitates glioma cell dissemination.
Petr VymolaElena Garcia-BorjaJakub ČervenkaEva BalaziovaBarbora VymolovaJana VeprkovaPetr VodickaHelena Kupcová SkalníkováRobert TomasDavid NetukaPetr BusekAleksi SedoPublished in: Brain pathology (Zurich, Switzerland) (2024)
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.
Keyphrases
- extracellular matrix
- blood brain barrier
- wound healing
- type iii
- tissue engineering
- poor prognosis
- mass spectrometry
- single cell
- cell migration
- liquid chromatography
- mesenchymal stem cells
- escherichia coli
- white matter
- bone marrow
- biofilm formation
- african american
- amino acid
- protein protein
- fine needle aspiration
- capillary electrophoresis
- cell adhesion