Starring role of toll-like receptor-4 activation in the gut-liver axis.

S. Carotti, M. Guarino, U. Vespasiani‐Gentilucci, S. Morini
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引用次数: 40

Abstract

Since the introduction of the term "gut-liver axis", many studies have focused on the functional links of intestinal microbiota, barrier function and immune responses to liver physiology. Intestinal and extra-intestinal diseases alter microbiota composition and lead to dysbiosis, which aggravates impaired intestinal barrier function via increased lipopolysaccharide translocation. The subsequent increased passage of gut-derived product from the intestinal lumen to the organ wall and bloodstream affects gut motility and liver biology. The activation of the toll-like receptor 4 (TLR-4) likely plays a key role in both cases. This review analyzed the most recent literature on the gut-liver axis, with a particular focus on the role of TLR-4 activation. Findings that linked liver disease with dysbiosis are evaluated, and links between dysbiosis and alterations of intestinal permeability and motility are discussed. We also examine the mechanisms of translocated gut bacteria and/or the bacterial product activation of liver inflammation and fibrogenesis via activity on different hepatic cell types.
toll样受体-4激活在肠-肝轴中的主要作用。
自“肠肝轴”一词被引入以来,许多研究都集中在肠道微生物群、屏障功能和免疫反应与肝脏生理的功能联系上。肠道和肠外疾病改变微生物群组成并导致生态失调,从而通过增加脂多糖易位加重肠道屏障功能受损。随后,肠源性产物从肠腔进入器官壁和血流的通道增加,影响肠道运动和肝脏生物学。toll样受体4 (TLR-4)的激活可能在这两种情况下都起着关键作用。这篇综述分析了最近关于肠肝轴的文献,特别关注TLR-4激活的作用。我们评估了肝脏疾病与生态失调相关的研究结果,并讨论了生态失调与肠道通透性和运动性改变之间的联系。我们还研究了易位肠道细菌和/或细菌产物通过对不同肝细胞类型的活性激活肝脏炎症和纤维化的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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