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The roles of Toll-like receptor 4 in the pathogenesis of pathogen-associated biliary fibrosis caused by Clonorchis sinensis

机译:Toll样受体4在华支睾吸虫病致病性胆纤维化发病机制中的作用

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摘要

Pathogen-associated biliary fibrosis (PABF) is a type of liver fibrosis characterized by injuries of cholangiocytes and extra cellular matrix (ECM) deposition around bile ducts caused by various bacteria, fungi, virus and parasites. Recent studies show that TLR4 plays an important role in several other types of liver fibrosis, but the mechanism of TLR4 in PABF is yet really unclear. In the present study, a PABF mouse model was established by a trematode infection-Clonorchis sinensis which dwells in the bile ducts and causes severe biliary fibrosis of mice. The results showed that the levels of collagen depositions, α-SMA and hydroxyproline (Hyp) contents in TLR4mut mice infected by C. sinensis were significantly lower than in those of TLR4wild ones. Furthermore, we found that the activation of TGF-β signaling was impaired in the TLR4mut mice, compared with wild mice when they were challenged to the same dose of C. sinensis metacercariae. Moreover, the mice with TLR4 mutation showed a decreased activation of hepatic stellate cells indicated by the expression of α-SMA, when compared with TLR4wild mice. These data demonstrate that TLR4 contributes to PABF caused by C. sinensis and TLR4 signaling may be a potential medical target for treatment of PABF.
机译:病原相关的胆汁纤维化(PABF)是一种肝纤维化,其特征是胆管细胞的损伤和胆管周围由多种细菌,真菌,病毒和寄生虫引起的细胞外基质(ECM)沉积。最近的研究表明,TLR4在几种其他类型的肝纤维化中也起着重要作用,但是PABF中TLR4的机制尚不清楚。在本研究中,由停留在胆管中并引起小鼠严重胆汁纤维化的吸虫感染-克氏克隆建立了PABF小鼠模型。结果显示,中华绒螯蟹感染的TLR4 mut 小鼠的胶原沉积,α-SMA和羟脯氨酸(Hyp)含量明显低于野生的TLR4 mut 小鼠。 >个。此外,我们发现与野生小鼠攻击相同剂量的中华cer虫相比,TLR4 mut 小鼠的TGF-β信号传导受到了损害。此外,与TLR4 野生小鼠相比,具有TLR4突变的小鼠表现出α-SMA表达降低了肝星状细胞的活化。这些数据表明TLR4有助于由中华假丝酵母引起的PABF,并且TLR4信号传导可能是治疗PABF的潜在医学靶标。

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