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首页> 外文期刊>American Journal of Physiology >Cellular Mechanisms of Tissue Fi-brosis. 5. Novel insights into liver fibrosis.
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Cellular Mechanisms of Tissue Fi-brosis. 5. Novel insights into liver fibrosis.

机译:组织纤维化的细胞机制。 5.对肝纤维化的新颖见解。

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摘要

Liver fibrosis is the common scarring reaction associated with chronic liver injury that results from prolonged parenchymal cell injury and/or inflammation. The fibro-genic response is characterized by progressive accumulation of extracellular matrix components enriched in fibrillar collagens and a failure of matrix turnover. This process is driven by a heterogeneous population of hepatic myofibroblasts, which mainly derive from hepatic stellate cells and portal fibroblasts. Regression of fibrosis can be achieved by the successful control of chronic liver injury, owing to termination of the fibrogenic reaction following clearance of hepatic myofibroblasts and restoration of fibrolytic pathways. Understanding of the complex network underlying liver fibrogenesis has allowed the identification of a large number of antifibrotic targets, but no antifi-brotic drug has as yet been approved. This review will highlight recent advances regarding the mechanisms that regulate liver fibrogenesis and fibrosis regression, with special focus on novel signaling pathways and the role of inflammatory cells. Translation of these findings to therapies will require continued efforts to develop multitarget therapeutic approaches that will improve the grim prognosis of liver cirrhosis.
机译:肝纤维化是与慢性肝损伤相关的常见瘢痕形成反应,其由长期的实质细胞损伤和/或炎症引起。纤维原性反应的特征在于富含纤维状胶原的细胞外基质组分的逐步积累和基质更新的失败。这个过程是由异质性肝成纤维细胞群体驱动的,其主要来源于肝星状细胞和门静脉成纤维细胞。通过成功控制慢性肝损伤可以实现纤维化的消退,这是由于清除肝成纤维细胞并恢复纤溶途径后纤维化反应的终止。对肝纤维化潜在基础的复杂网络的了解已允许鉴定大量抗纤维化靶标,但尚未批准任何抗纤维化药物。这篇综述将重点介绍调节肝脏纤维发生和纤维化消退的机制的最新进展,特别关注新型信号通路和炎症细胞的作用。将这些发现转化为疗法将需要继续努力,以开发可改善肝硬化严峻预后的多靶点治疗方法。

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