Microglia are continuously activated in the circumventricular organs of mouse brain

J Neuroimmunol. 2019 Jun 15:331:74-86. doi: 10.1016/j.jneuroim.2017.10.008. Epub 2017 Oct 19.

Abstract

Microglia are the primary resident immune cells of the brain parenchyma and transform into the amoeboid form in the "activated state" under pathological conditions from the ramified form in the "resting state" under physiologically healthy conditions. In the present study, we found that microglia in the circumventricular organs (CVOs) of adult mice displayed the amoeboid form with fewer branched cellular processes even under normal conditions; however, those in other brain regions showed the ramified form, which is characterized by well-branched and dendritic cellular processes. Moreover, microglia in the CVOs showed the strong protein expression of the M1 markers CD16/32 and CD86 and M2 markers CD206 and Ym1 without any pathological stimulation. Thus, the present results indicate that microglia in the CVOs of adult mice are morphologically and functionally activated under normal conditions, possibly due to the specialized features of the CVOs, namely, the entry of blood-derived molecules into parenchyma through fenestrated capillaries and the presence of neural stem cells.

Keywords: Amoeboid; Brain; CD16/32; CD206; CD86; Microglia; Ym1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Antigens, CD / genetics
  • Capillaries / physiology
  • Capillary Permeability
  • Cell Shape
  • Circumventricular Organs / blood supply
  • Circumventricular Organs / cytology*
  • Gene Expression Regulation
  • Lectins / physiology
  • Lectins, C-Type / physiology
  • Macrophages / physiology
  • Male
  • Mannose Receptor
  • Mannose-Binding Lectins / physiology
  • Mice
  • Mice, Inbred C57BL
  • Microglia / cytology
  • Microglia / physiology*
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics
  • Nestin / deficiency
  • Neural Stem Cells / cytology
  • Receptors, Cell Surface / physiology
  • beta-N-Acetylhexosaminidases / physiology

Substances

  • Antigens, CD
  • Lectins
  • Lectins, C-Type
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • Receptors, Cell Surface
  • Chil3 protein, mouse
  • beta-N-Acetylhexosaminidases