| Literature DB >> 29445035 |
Joseph Juliano1, Orlando Gil2, Andrea Hawkins-Daarud3, Sonal Noticewala4, Russell C Rockne5, Jill Gallaher6, Susan Christine Massey3, Peter A Sims7, Alexander R A Anderson6, Kristin R Swanson3, Peter Canoll2.
Abstract
Microglia are a major cellular component of gliomas, and abundant in the centre of the tumour and at the infiltrative margins. While glioma is a notoriously infiltrative disease, the dynamics of microglia and glioma migratory patterns have not been well characterized. To investigate the migratory behaviour of microglia and glioma cells at the infiltrative edge, we performed two-colour time-lapse fluorescence microscopy of brain slices generated from a platelet-derived growth factor-B (PDGFB)-driven rat model of glioma, in which glioma cells and microglia were each labelled with one of two different fluorescent markers. We used mathematical techniques to analyse glioma cells and microglia motility with both single cell tracking and particle image velocimetry (PIV). Our results show microglia motility is strongly correlated with the presence of glioma, while the correlation of the speeds of glioma cells and microglia was variable and weak. Additionally, we showed that microglia and glioma cells exhibit different types of diffusive migratory behaviour. Microglia movement fit a simple random walk, while glioma cell movement fits a super diffusion pattern. These results show that glioma cells stimulate microglia motility at the infiltrative margins, creating a correlation between the spatial distribution of glioma cells and the pattern of microglia motility.Entities:
Keywords: PDGF rat model; anomalous diffusion; glioblastoma; particle image velocimetry; time lapse microscopy
Mesh:
Year: 2018 PMID: 29445035 PMCID: PMC5832721 DOI: 10.1098/rsif.2017.0582
Source DB: PubMed Journal: J R Soc Interface ISSN: 1742-5662 Impact factor: 4.118