Detection and functional evaluation of arginase-1 isolated from human PMNs and murine MDSC

Methods Enzymol. 2020:632:193-213. doi: 10.1016/bs.mie.2019.07.022. Epub 2019 Aug 12.

Abstract

Immunotherapy has emerged as a potent alternative for cancer treatment, unfortunately, the clinical benefit remains limited to few patients and immunotherapy resistance due to immunosuppressive tumor microenvironment represents the major reason of such a failure. Arginase-1 is one of the enzymes contributing to the establishment of such immunosuppression. Among the human immune cells, polymorphonuclear cells (PMNs) represent the major source of arginase-1, while myeloid-derived suppressor cells (MDSCs) are the main arginase-1 producing cells in mice. Due to arginase-1 potential impact in dampening the immune response, there is a growing interest in assaying arginase-1 levels and functions. Thus, in this chapter we propose how to evaluate the expression and activity of arginase in human peripheral blood-derived PMNs and in MDSCs isolated from tumor-bearing mice.

Keywords: Arginase; Arginase inhibitors; Human neutrophils; Murine myeloid-derived suppressor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginase / analysis
  • Arginase / immunology*
  • Cell Proliferation
  • Cells, Cultured
  • Flow Cytometry / methods
  • Fluorescent Antibody Technique / methods
  • Humans
  • Mice
  • Myeloid-Derived Suppressor Cells / immunology*
  • Neoplasms / immunology
  • Neutrophils / immunology*
  • T-Lymphocytes / immunology
  • Tumor Microenvironment

Substances

  • ARG1 protein, human
  • Arg1 protein, mouse
  • Arginase