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Notch-Hes1 信号激活在先天性肝内胆管扩张症和多囊肝病中的作用。

Notch-Hes1 signaling activation in Caroli disease and polycystic liver disease.

机构信息

Department of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Department of Diagnostic Pathology, Kanazawa University Hospital, Kanazawa, Japan.

出版信息

Pathol Int. 2021 Aug;71(8):521-529. doi: 10.1111/pin.13130. Epub 2021 Jun 24.

Abstract

The Notch signaling pathway plays a key role in the morphogenesis of the biliary tree, but its involvement in cystic biliary diseases, such as Caroli disease (CD) and polycystic liver disease (PLD), has yet to be determined. Immunostaining was performed using liver sections of CD and PLD, and the results were compared with those of congenital hepatic fibrosis (CHF) and von Meyenburg complex (VMC). The expression of Notch receptor 1 (Notch1) was increased in the nuclei of biliary epithelial cells in all cases of CD and PLD, whereas it remained at a low level in CHF and VMC. In addition, Notch2 and Notch3 were preferably expressed in the nuclei of biliary epithelial cells of PLD. Accordingly, the Notch effector Hes1 was highly expressed in biliary epithelial cells of CD and PLD, and the cell proliferative activity was significantly higher in CD and PLD. The expression of the Notch ligand Delta-like 1 was significantly increased in biliary epithelial cells of CD and PLD, which may be causally associated with the nuclear overexpression of Notch1 and Hes1. These results indicate that aberrant activation of the Notch-Hes1 signaling pathway may be responsible for the progression of biliary cystogenesis in CD and PLD.

摘要

Notch 信号通路在胆管树的形态发生中起着关键作用,但它在胆管囊性疾病(如 Caroli 病(CD)和多囊肝病(PLD))中的作用尚未确定。使用 CD 和 PLD 的肝组织切片进行免疫染色,并将结果与先天性肝纤维化(CHF)和 von Meyenburg 复合体(VMC)进行比较。Notch 受体 1(Notch1)在所有 CD 和 PLD 病例的胆管上皮细胞的核中表达增加,而在 CHF 和 VMC 中表达水平较低。此外,Notch2 和 Notch3 优选在 PLD 的胆管上皮细胞的核中表达。因此,Notch 效应物 Hes1 在 CD 和 PLD 的胆管上皮细胞中高度表达,CD 和 PLD 的细胞增殖活性显著升高。Notch 配体 Delta-like 1 在 CD 和 PLD 的胆管上皮细胞中的表达显著增加,这可能与 Notch1 和 Hes1 的核过表达有因果关系。这些结果表明,Notch-Hes1 信号通路的异常激活可能导致 CD 和 PLD 中胆管囊状发生的进展。

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