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Extracellular matrix bioengineering and systems biology approaches in liver disease

机译:肝病中的细胞外基质生物工程和系统生物学方法

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The extracellular matrix (ECM) in the liver as well as in many organs comprises a peripheral network linking numerous macromolecules typically classified into collagens, microfibrillar proteins, proteoglycans, chemo-kines, growth factors and glycoproteins. In addition to its role as an essential structural and physiological component, it plays a vital role in driving key cellular events such as cell adhesion, migration, proliferation, differentiation and survival. Any structural inherited or acquireddefect and/or metabolic or pathologic alteration in the hepatic ECM may cause cellular and organ responses leading to the development or progression of liver disease. Therefore, the ECM molecules are key players in tissue engraftment and in the pathophysiology of liver disease. In this review we provide a snapshot on current efforts for understanding its role in physiological and non-physiological states, by describing how tissue engineering platforms can enhance in vitro and in vivo models of liver disease, by providing examples where bioengineered ECM can serve as systems biology approaches to study the ECM, and then by evaluating pathological protein regulatory networks in the liver using systems biology tools. These approaches hold great promise for future research.
机译:肝脏以及许多器官中的细胞外基质(ECM)包含一个外围网络,该外围网络将众多大分子连接起来,这些大分子通常分为胶原蛋白,微纤维蛋白,蛋白聚糖,化学因子,生长因子和糖蛋白。除了作为重要的结构和生理成分发挥作用外,它在驱动关键的细胞事件(例如细胞粘附,迁移,增殖,分化和存活)中也起着至关重要的作用。肝ECM中任何结构性遗传或获得性缺陷和/或代谢或病理改变都可能引起细胞和器官反应,从而导致肝脏疾病的发展或进展。因此,ECM分子是组织植入和肝病病理生理学中的关键角色。在这篇综述中,我们通过描述组织工程平台如何通过生物工程ECM可以作为系统的实例来描述组织工程平台如何增强肝脏疾病的体外和体内模型,从而简要介绍了当前为了解其在生理状态和非生理状态中的作用所做的努力。生物学方法研究ECM,然后使用系统生物学工具评估肝脏中的病理性蛋白质调节网络。这些方法对未来的研究具有广阔的前景。

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