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Low-dose lipopolysaccharide as an immune regulator for homeostasis maintenance in the central nervous system through transformation to neuroprotective microglia

Journal

NEURAL REGENERATION RESEARCH
Volume 16, Issue 10, Pages 1928-+

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.308067

Keywords

cognitive impairment; endotoxin; lipopolysaccharide; low-dose; microglia; neuroprotection; oral administration; preconditioning; tolerance; trained innate immunity

Funding

  1. Control of Innate Immunity Technology Research Association
  2. Cross-ministerial Strategic Innovation Promotion Program from the Council for Science from Technology and Innovation (CSTI) in Cabinet Office of Japanese Government [14533073]
  3. National Agriculture and Food Research Organization (NARO)

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Microglia, tissue-resident macrophages in the brain, play a central role in brain innate immunity. Studies suggest that lipopolysaccharide, known as an endotoxin, can ameliorate Alzheimer's disease pathology by transforming microglia into a neuroprotective phenotype. Furthermore, controlled immune training with low-dose lipopolysaccharide may have neuroprotective effects by modulating microglial function.
Microglia, which are tissue-resident macrophages in the brain, play a central role in the brain innate immunity and contribute to the maintenance of brain homeostasis. Lipopolysaccharide is a component of the outer membrane of gram-negative bacteria, and activates immune cells including microglia via Toll-like receptor 4 signaling. Lipopolysaccharide is generally known as an endotoxin, as administration of high-dose lipopolysaccharide induces potent systemic inflammation. Also, it has long been recognized that lipopolysaccharide exacerbates neuroinflammation. In contrast, our study revealed that oral administration of lipopolysaccharide ameliorates Alzheimer's disease pathology and suggested that neuroprotective microglia are involved in this phenomenon. Additionally, other recent studies have accumulated evidence demonstrating that controlled immune training with low-dose lipopolysaccharide prevents neuronal damage by transforming the microglia into a neuroprotective phenotype. Therefore, lipopolysaccharide may not a mere inflammatory inducer, but an immunomodulator that can lead to neuroprotective effects in the brain. In this review, we summarized current studies regarding neuroprotective microglia transformed by immune training with lipopolysaccharide. We state that microglia transformed by lipopolysaccharide preconditioning cannot simply be characterized by their general suppression of proinflammatory mediators and general promotion of anti-inflammatory mediators, but instead must be described by their complex profile comprising various molecules related to inflammatory regulation, phagocytosis, neuroprotection, anti-apoptosis, and antioxidation. In addition, microglial transformation seems to depend on the dose of lipopolysaccharide used during immune training. Immune training of neuroprotective microglia using low-dose lipopolysaccharide, especially through oral lipopolysaccharide administration, may represent an innovative prevention or treatment for neurological diseases; however more vigorous studies are still required to properly modulate these treatments.

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