Expression of iNOS, CD163 and ARG-1 taken as M1 and M2 markers of microglial polarization in human glioblastoma and the surrounding normal parenchyma

Lucia Lisi, Gabriella Maria Pia Ciotti, D. Braun, S. Kalinin, Diego Curro', Cinzia Dello Russo, Antonella Coli, Annunziato Mangiola, Carmelo Anile, D. L. Feinstein, Pierluigi Navarra*

*Corresponding author

Research output: Contribution to journalArticle

70 Citations (Scopus)

Abstract

Microglia and macrophages appear to be the most common cells in the GBM microenvironment. In the present study we investigated the status of macrophages/microglia activation in surgical specimens from 41 patients diagnosed with grade IV GBM. For each patient we analyzed both the center of tumor and the parenchyma surrounding the tumor. The specimens were stained for: i) IBA1, a 17-kDa EF hand protein specifically expressed in microglia/macrophages ii) CD163, a cell surface antigen associated with M2 phenotype; iii) iNOS, taken as a functional marker of M1 phenotype, and iv) ARG-I, taken as a functional marker of M2 phenotype. Staining was scored in a double-blinded score on a scale from 0 to 5. Our results suggest that CD163 expression is higher within the tumor than in surrounding periphery in both male and female patients; while iNOS is higher within the tumor in males, no significant difference was found for ARG-1. In addition, analyzing the data in TGCA database, we found that CD163 expression was significantly and inversely correlated with mean survival times, with average survival times ranging from 448 days in patients having low expression, to 319 in mid, and 353 in patients with high CD163 expressing tumors. In contrast, no significant association was found between survival time and ARG-1 or iNOS expression.
Original languageEnglish
Pages (from-to)106-112
Number of pages7
JournalNeuroscience Letters
Volume645
DOIs
Publication statusPublished - 2017

Keywords

  • ARG-I
  • CD163
  • Glioblastoma
  • M1 polarization
  • M2 polarization
  • Microglia
  • Neuroscience (all)
  • Periphery
  • Tumor
  • iNOS

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