Fibrillar extracellular matrix produced by pericyte‐like cells facilitates glioma cell dissemination

Author:

Vymola Petr1ORCID,Garcia‐Borja Elena1ORCID,Cervenka Jakub23ORCID,Balaziova Eva1ORCID,Vymolova Barbora1ORCID,Veprkova Jana1ORCID,Vodicka Petr2ORCID,Skalnikova Helena23ORCID,Tomas Robert4ORCID,Netuka David5ORCID,Busek Petr1ORCID,Sedo Aleksi1ORCID

Affiliation:

1. Laboratory of Cancer Cell Biology, Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine Charles University Prague Czech Republic

2. Laboratory of Applied Proteome Analyses, Research Center PIGMOD Institute of Animal Physiology and Genetics of the Czech Academy of Sciences Liběchov Czech Republic

3. Laboratory of proteomics, Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine Charles University Prague Czech Republic

4. Department of Neurosurgery Na Homolce Hospital Prague Czech Republic

5. Department of Neurosurgery and Neurooncology, First Faculty of Medicine Charles University and Military University Hospital Prague Czech Republic

Abstract

AbstractGliomagenesis 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.

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Ministerstvo Zdravotnictví Ceské Republiky

Univerzita Karlova v Praze

Publisher

Wiley

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