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从骨免疫学到骨微生物学:微生物群和免疫系统如何调节骨骼。

From Osteoimmunology to Osteomicrobiology: How the Microbiota and the Immune System Regulate Bone.

机构信息

Division of Endocrinology, Metabolism and Lipids, Department of Medicine, Emory University, 101 Woodruff Circle, Room 1309, Atlanta, GA, 30322, USA.

Immunology and Molecular Pathogenesis Program, Emory University, Atlanta, GA, USA.

出版信息

Calcif Tissue Int. 2018 May;102(5):512-521. doi: 10.1007/s00223-017-0321-0. Epub 2017 Oct 10.

Abstract

Osteomicrobiology refers to the role of microbiota in bone health and the mechanisms by which the microbiota regulates post-natal skeletal development, bone aging, and pathologic bone loss. Here, we review recent reports linking gut microbiota to changes in bone phenotype. A pro-inflammatory cytokine milieu drives bone resorption in conditions such as sex steroid hormone deficiency. The response of the immune system to activation by the microbiome results in increased circulating osteoclastogenic cytokines in a T cell-dependent mechanism. Additionally, gut microbiota affect bone homeostasis through nutrient absorption, mediation of the IGF-1 pathway, and short chain fatty acid and metabolic products. Manipulation of microbiota through prebiotics or probiotics reduces inflammatory cytokine production, leading to changes in bone density. One mechanism of probiotic action is through upregulating tight junction proteins, increasing the strength of the gut epithelial layer, and leading to less antigen presentation and less activation of intestinal immune cells. Thus, prebiotics or probiotics may represent a future therapeutic avenue for ameliorating the risk of postmenopausal bone loss in humans.

摘要

骨微生物学是指微生物群在骨骼健康中的作用,以及微生物群调节出生后骨骼发育、骨骼衰老和病理性骨质流失的机制。在这里,我们回顾了最近将肠道微生物群与骨骼表型变化联系起来的报告。在性激素缺乏等情况下,促炎细胞因子环境会驱动破骨细胞吸收。免疫系统对微生物组激活的反应导致破骨细胞生成细胞因子在 T 细胞依赖性机制中循环增加。此外,肠道微生物群通过营养吸收、IGF-1 途径以及短链脂肪酸和代谢产物来影响骨稳态。通过使用益生元或益生菌来操纵微生物群可以减少炎症细胞因子的产生,从而导致骨密度的变化。益生菌作用的一种机制是通过上调紧密连接蛋白,增加肠道上皮层的强度,从而减少抗原呈递和肠道免疫细胞的激活。因此,益生元或益生菌可能代表一种未来的治疗途径,可以改善绝经后女性的骨质流失风险。

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