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肝细胞的多倍体化:对肝脏疾病发病机制的见解

Polyploidization of Hepatocytes: Insights into the Pathogenesis of Liver Diseases.

作者信息

Kim Ju-Yeon, Choi Haena, Kim Hyeon-Ji, Jee Yelin, Noh Minsoo, Lee Mi-Ock

机构信息

College of Pharmacy, Seoul National University, Seoul 00826, Republic of Korea.

Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 00826, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2022 Sep 1;30(5):391-398. doi: 10.4062/biomolther.2022.070. Epub 2022 Jul 5.

Abstract

Polyploidization is a process by which cells are induced to possess more than two sets of chromosomes. Although polyploidization is not frequent in mammals, it is closely associated with development and differentiation of specific tissues and organs. The liver is one of the mammalian organs that displays ploidy dynamics in physiological homeostasis during its development. The ratio of polyploid hepatocytes increases significantly in response to hepatic injury from aging, viral infection, iron overload, surgical resection, or metabolic overload, such as that from non-alcoholic fatty liver diseases (NAFLDs). One of the unique features of NAFLD is the marked heterogeneity of hepatocyte nuclear size, which is strongly associated with an adverse liver-related outcome, such as hepatocellular carcinoma, liver transplantation, and liver-related death. Thus, hepatic polyploidization has been suggested as a potential driver in the progression of NAFLDs that are involved in the control of the multiple pathogenicity of the diseases. However, the importance of polyploidy in diverse pathophysiological contexts remains elusive. Recently, several studies reported successful improvement of symptoms of NAFLDs by reducing pathological polyploidy or by controlling cell cycle progression in animal models, suggesting that better understanding the mechanisms of pathological hepatic polyploidy may provide insights into the treatment of hepatic disorders.

摘要

多倍体化是一个促使细胞拥有两套以上染色体的过程。尽管多倍体化在哺乳动物中并不常见,但它与特定组织和器官的发育及分化密切相关。肝脏是在其发育过程中生理稳态下呈现倍性动态变化的哺乳动物器官之一。多倍体肝细胞的比例会因衰老、病毒感染、铁过载、手术切除或代谢过载(如非酒精性脂肪性肝病(NAFLD)所致)引起的肝损伤而显著增加。NAFLD的一个独特特征是肝细胞核大小的显著异质性,这与不良肝脏相关结局(如肝细胞癌、肝移植和肝脏相关死亡)密切相关。因此,肝多倍体化被认为是参与控制NAFLD多种致病性进展的潜在驱动因素。然而,多倍体在不同病理生理背景下的重要性仍不清楚。最近,几项研究报告称,通过减少病理多倍体或控制动物模型中的细胞周期进程,成功改善了NAFLD的症状,这表明更好地理解病理性肝多倍体的机制可能为肝脏疾病的治疗提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c364/9424332/a2a0ef6c3ff4/bt-30-5-391-f1.jpg

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