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胆管性恐慌:肝内胆管细胞如何应对应激和损伤。

Panic at the Bile Duct: How Intrahepatic Cholangiocytes Respond to Stress and Injury.

机构信息

Division of Digestive Diseases, Department of Medicine, Emory University, Atlanta, Georgia; Graduate Program in Biochemistry, Cell and Developmental Biology, Emory University, Atlanta, Georgia.

Division of Digestive Diseases, Department of Medicine, Emory University, Atlanta, Georgia.

出版信息

Am J Pathol. 2023 Oct;193(10):1440-1454. doi: 10.1016/j.ajpath.2023.02.012. Epub 2023 Mar 2.

Abstract

In the liver, biliary epithelial cells (BECs) line intrahepatic bile ducts (IHBDs) and are primarily responsible for modifying and transporting hepatocyte-produced bile to the digestive tract. BECs comprise only 3% to 5% of the liver by cell number but are critical for maintaining choleresis through homeostasis and disease. To this end, BECs drive an extensive morphologic remodeling of the IHBD network termed ductular reaction (DR) in response to direct injury or injury to the hepatic parenchyma. BECs are also the target of a broad and heterogenous class of diseases termed cholangiopathies, which can present with phenotypes ranging from defective IHBD development in pediatric patients to progressive periductal fibrosis and cancer. DR is observed in many cholangiopathies, highlighting overlapping similarities between cell- and tissue-level responses by BECs across a spectrum of injury and disease. The following core set of cell biological BEC responses to stress and injury may moderate, initiate, or exacerbate liver pathophysiology in a context-dependent manner: cell death, proliferation, transdifferentiation, senescence, and acquisition of neuroendocrine phenotype. By reviewing how IHBDs respond to stress, this review seeks to highlight fundamental processes with potentially adaptive or maladaptive consequences. A deeper understanding of how these common responses contribute to DR and cholangiopathies may identify novel therapeutic targets in liver disease.

摘要

在肝脏中,胆管上皮细胞 (BEC) 排列在肝内胆管 (IHBD) 内,主要负责修饰和将肝细胞产生的胆汁转运至消化道。BEC 细胞数量仅占肝脏的 3%至 5%,但对于通过动态平衡和疾病维持胆汁分泌至关重要。为此,BEC 会响应直接损伤或肝实质损伤,驱动 IHBD 网络的广泛形态重塑,称为胆管反应 (DR)。BEC 也是广泛且异质的胆管疾病的靶标,这些疾病可表现为从儿科患者 IHBD 发育缺陷到进行性周围胆管纤维化和癌症的各种表型。在许多胆管疾病中都观察到 DR,突出了 BEC 在一系列损伤和疾病中对细胞和组织水平反应的重叠相似性。以下是 BEC 对压力和损伤的一系列核心细胞生物学反应,这些反应可能以依赖于上下文的方式调节、引发或加重肝病理生理学:细胞死亡、增殖、转分化、衰老和获得神经内分泌表型。通过回顾 IHBD 对压力的反应,本综述旨在强调具有潜在适应性或不适应性后果的基本过程。更深入地了解这些常见反应如何导致 DR 和胆管疾病,可能会确定肝脏疾病的新治疗靶点。

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