Microglial lysophosphatidic acid promotes glioblastoma proliferation and migration via LPA 1 receptor

• Published in: Journal of neurochemistry Vol. 156; no. 4; pp. 499 - 512
• Main Authors: Amaral, Rackele F, Geraldo, Luiz H M, Einicker-Lamas, Marcelo, E Spohr, Tania C L de S, Mendes, Fabio, Lima, Flavia R S
• Format: Journal Article
• Language: English
• Published: England 01.02.2021
• Subjects: Animals; Brain Neoplasms - metabolism; Brain Neoplasms - pathology; Cell Movement - physiology; Cell Proliferation - physiology; Cells, Cultured; Female; Glioblastoma - metabolism; Glioblastoma - pathology; Humans; Lysophospholipids - metabolism; Male; Mice; Microglia - metabolism; Microglia - pathology; Receptors, Lysophosphatidic Acid - biosynthesis; tumor migration; tumor proliferation; glioblastoma; Lysophosphatidic acid; microglia; LPA1
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/jnc.15097

Glioblastomas (GBMs) are highly aggressive primary brain tumors characterized by cellular heterogeneity, insensitivity to chemotherapy and poor patient survival. Lysophosphatidic acid (LPA) is a lysophospholipid that acts as a bioactive signaling molecule and plays important roles in diverse biological events during development and disease, including several cancer types. Microglial cells, the resident macrophages of the central nervous system, express high levels of Autotaxin (ATX,Enpp2), an enzyme that synthetizes LPA. Our study aimed to investigate the role of LPA on tumor growth and invasion in the context of microglia-GBM interaction. First, through bioinformatics studies, patient data analysis demonstrated that more aggressive GBM expressed higher levels of ENPP2, which was also associated with worse patient prognosis with proneural GBM. Using GBM-microglia co-culture system we then demonstrated that GBM secreted factors were able to increase LPA and ATX in microglia, which could be further enhanced by hypoxia. On the other hand, interaction with microglial cells also increased ATX expression in GBM. Furthermore, microglial-induced GBM proliferation and migration could be inhibited by pharmacological inhibition of LPA , suggesting that microglial-derived LPA could support tumor growth and invasion. Finally, increased LPA expression was observed in GBM comparing with other gliomas and could be also associated with worse patient survival. These results show for the first time a microglia-GBM interaction through the LPA pathway with relevant implications for tumor progression. A better understanding of this interaction can lead to the development of new therapeutic strategies setting LPA as a potential target for GBM treatment.