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Publication : Endogenous brain pericytes are widely activated and contribute to mouse glioma microvasculature.

First Author  Svensson A Year  2015
Journal  PLoS One Volume  10
Issue  4 Pages  e0123553
PubMed ID  25875288 Mgi Jnum  J:233497
Mgi Id  MGI:5784837 Doi  10.1371/journal.pone.0123553
Citation  Svensson A, et al. (2015) Endogenous brain pericytes are widely activated and contribute to mouse glioma microvasculature. PLoS One 10(4):e0123553
abstractText  Glioblastoma multiforme (GBM) is the most common brain tumor in adults. It presents an extremely challenging clinical problem, and treatment very frequently fails due to the infiltrative growth, facilitated by extensive angiogenesis and neovascularization. Pericytes constitute an important part of the GBM microvasculature. The contribution of endogenous brain pericytes to the tumor vasculature in GBM is, however, unclear. In this study, we determine the site of activation and the extent of contribution of endogenous brain pericytes to the GBM vasculature. GL261 mouse glioma was orthotopically implanted in mice expressing green fluorescent protein (GFP) under the pericyte marker regulator of G protein signaling 5 (RGS5). Host pericytes were not only activated within the glioma, but also in cortical areas overlying the tumor, the ipsilateral subventricular zone and within the hemisphere contralateral to the tumor. The host-derived activated pericytes that infiltrated the glioma were mainly localized to the tumor vessel wall. Infiltrating GFP positive pericytes co-expressed the pericyte markers platelet-derived growth factor receptor-beta (PDGFR-beta) and neuron-glial antigen 2. Interestingly, more than half of all PDGFR-beta positive pericytes within the tumor were contributed by the host brain. We did not find any evidence that RGS5 positive pericytes adopt another phenotype within glioma in this paradigm. We conclude that endogenous pericytes become activated in widespread areas of the brain in response to an orthotopic mouse glioma. Host pericytes are recruited into the tumor and constitute a major part of the tumor pericyte population.
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