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低剂量脂多糖作为一种免疫调节剂,通过转化为具有神经保护作用的小胶质细胞来维持中枢神经系统的内环境稳定。

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

作者信息

Mizobuchi Haruka, Soma Gen-Ichiro

机构信息

Control of Innate Immunity, Technology Research Association, Kagawa, Japan.

Control of Innate Immunity, Technology Research Association; Macrophi Inc., Kagawa; Research Institute for Healthy Living, Niigata University of Pharmacy and Applied Life Sciences, Niigata, Japan.

出版信息

Neural Regen Res. 2021 Oct;16(10):1928-1934. doi: 10.4103/1673-5374.308067.

Abstract

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.

摘要

小胶质细胞是脑内驻留组织的巨噬细胞,在脑固有免疫中起核心作用,并有助于维持脑内稳态。脂多糖是革兰氏阴性菌外膜的一种成分,可通过Toll样受体4信号通路激活包括小胶质细胞在内的免疫细胞。脂多糖通常被称为内毒素,因为高剂量脂多糖的给药会引发强烈的全身炎症。此外,长期以来人们一直认识到脂多糖会加剧神经炎症。相比之下,我们的研究表明口服脂多糖可改善阿尔茨海默病病理,并提示具有神经保护作用的小胶质细胞参与了这一现象。此外,最近的其他研究积累了证据,表明用低剂量脂多糖进行可控的免疫训练可通过将小胶质细胞转化为神经保护表型来预防神经元损伤。因此,脂多糖可能不仅仅是一种炎症诱导剂,而是一种能够在脑中产生神经保护作用的免疫调节剂。在这篇综述中,我们总结了目前关于通过脂多糖免疫训练转化为神经保护型小胶质细胞的研究。我们指出,经脂多糖预处理转化的小胶质细胞不能简单地通过其对促炎介质的普遍抑制和对抗炎介质的普遍促进来表征,而必须通过其包含与炎症调节、吞噬作用、神经保护、抗凋亡和抗氧化相关的各种分子的复杂特征来描述。此外,小胶质细胞的转化似乎取决于免疫训练期间使用的脂多糖剂量。使用低剂量脂多糖对神经保护型小胶质细胞进行免疫训练,尤其是通过口服脂多糖给药,可能代表了一种针对神经疾病的创新预防或治疗方法;然而,仍需要更深入的研究来适当调节这些治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef8/8343302/51a046bcf0df/NRR-16-1928-g001.jpg

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