Selective proliferative response of microglia to alternative polarization signals

• Published in: Journal of neuroinflammation Vol. 14; no. 1; p. 236
• Main Authors: Pepe, Giovanna, De Maglie, Marcella, Minoli, Lucia, Villa, Alessandro, Maggi, Adriana, Vegeto, Elisabetta
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 04-12-2017; BioMed Central; BMC
• Subjects: 17β-Estradiol; Amyotrophic lateral sclerosis; Analysis; Astrocytes; Brain; Cell cycle; Cell growth; Cell proliferation; Cell self-renewal; Central nervous system; Cerebrospinal fluid; Cytokines; Disease; Estradiol; Estrogen; Estrogens; Flow cytometry; Gene expression; Growth factors; Homeostasis; Immune system; Inflammation; Interleukin 4; Interleukins; Laboratory animals; Macrophage colony-stimulating factor; Macrophages; Microglia; Myeloid cells; Phenotypes; Polarization; Proliferation; RNA; Interleukin-4; Proliferation; Estrogen; Microglia
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/s12974-017-1011-6

Microglia are resident myeloid cells of the central nervous system (CNS) that are maintained by self-renewal and actively participate in tissue homeostasis and immune defense. Under the influence of endogenous or pathological signals, microglia undertake biochemical transformations that are schematically classified as the pro-inflammatory M1 phenotype and the alternatively activated M2 state. Dysregulated proliferation of M1-activated microglia has detrimental effects, while an increased number of microglia with the alternative, pro-resolving phenotype might be beneficial in brain pathologies; however, the proliferative response of microglia to M2 signals is not yet known. We thus evaluated the ability of interleukin-4 (IL-4), a typical M2 and proliferative signal for peripheral macrophages, to induce microglia proliferation and compared it with other proliferative and M2 polarizing stimuli for macrophages, namely colony-stimulating factor-1 (CSF-1) and the estrogen hormone, 17β-estradiol (E
).
Recombinant IL-4 was delivered to the brain of adult mice by intracerebroventricular (i.c.v.) injection; whole brain areas or ex vivo-sorted microglia were analyzed by real-time PCR for assessing the mRNA levels of genes related with cell proliferation (Ki67, CDK-1, and CcnB2) and M2 polarization (Arg1, Fizz1, Ym-1) or by FACS analyses of in vivo BrdU incorporation in microglia. Primary cultures of microglia and astrocytes were also tested for proliferative effects.
Our results show that IL-4 only slightly modified the expression of cell cycle-related genes in some brain areas but not in microglia, where it strongly enhanced M2 gene expression; on the contrary, brain delivery of CSF-1 triggered proliferation as well as M2 polarization of microglia both in vivo and in vitro. Similar to IL-4, the systemic E
administration failed to induce microglia proliferation while it increased M2 gene expression.
Our data show that, in contrast to the wider responsiveness of peripheral macrophages, microglia proliferation is stimulated by selected M2 polarizing stimuli suggesting a role for the local microenvironment and developmental origin of tissue macrophages in regulating self-renewal following alternative activating stimuli.