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非经典 Wnt 信号通路通过平面细胞极性受体调节胆道疾病的瘢痕形成。

Non-canonical Wnt signalling regulates scarring in biliary disease via the planar cell polarity receptors.

机构信息

MRC Human Genetics Unit, Institute for Genetic and Molecular Medicine, Edinburgh, UK.

Infectious Diseases and Immune Defence, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia.

出版信息

Nat Commun. 2020 Jan 23;11(1):445. doi: 10.1038/s41467-020-14283-3.

Abstract

The number of patients diagnosed with chronic bile duct disease is increasing and in most cases these diseases result in chronic ductular scarring, necessitating liver transplantation. The formation of ductular scaring affects liver function; however, scar-generating portal fibroblasts also provide important instructive signals to promote the proliferation and differentiation of biliary epithelial cells. Therefore, understanding whether we can reduce scar formation while maintaining a pro-regenerative microenvironment will be essential in developing treatments for biliary disease. Here, we describe how regenerating biliary epithelial cells express Wnt-Planar Cell Polarity signalling components following bile duct injury and promote the formation of ductular scars by upregulating pro-fibrogenic cytokines and positively regulating collagen-deposition. Inhibiting the production of Wnt-ligands reduces the amount of scar formed around the bile duct, without reducing the development of the pro-regenerative microenvironment required for ductular regeneration, demonstrating that scarring and regeneration can be uncoupled in adult biliary disease and regeneration.

摘要

被诊断患有慢性胆管疾病的患者人数正在增加,在大多数情况下,这些疾病会导致慢性胆管瘢痕形成,从而需要进行肝移植。胆管瘢痕的形成会影响肝功能;然而,产生瘢痕的门脉纤维母细胞也提供了重要的指导信号,以促进胆管上皮细胞的增殖和分化。因此,了解我们是否可以在维持促再生微环境的同时减少瘢痕形成,对于开发胆管疾病的治疗方法至关重要。在这里,我们描述了再生的胆管上皮细胞在胆管损伤后如何表达 Wnt-Planar Cell Polarity 信号传导成分,并通过上调促纤维化细胞因子和正向调节胶原蛋白沉积来促进胆管的瘢痕形成。抑制 Wnt-配体的产生可减少胆管周围形成的瘢痕量,而不会减少胆管再生所需的促再生微环境的发育,这表明在成人胆管疾病和再生中可以将瘢痕形成和再生分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f0/6978415/998fdcc98144/41467_2020_14283_Fig1_HTML.jpg

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