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改变肝细胞胞质内细胞内信号通路的蛋白质过度表达,形成马洛里-登克小体。

Over expression of proteins that alter the intracellular signaling pathways in the cytoplasm of the liver cells forming Mallory-Denk bodies.

作者信息

Afifiyan N, Tillman B, French B A, Masouminia M, Samadzadeh S, French S W

机构信息

Department of Pathology, Harbor UCLA Medical Center and Los Angeles BioMedical Institute, 1000W, Carson, Torrance, CA 90509, United States.

Department of Pathology, Harbor UCLA Medical Center and Los Angeles BioMedical Institute, 1000W, Carson, Torrance, CA 90509, United States.

出版信息

Exp Mol Pathol. 2017 Feb;102(1):106-114. doi: 10.1016/j.yexmp.2017.01.011. Epub 2017 Jan 13.

Abstract

In this study, liver biopsy sections fixed in formalin and embedded in paraffin (FFPE) from patients with alcoholic hepatitis (AH) were used. The results showed that the expression of the SYK protein was up regulated by RNA-seq and real time PCR analyses in the alcoholic hepatitis patients compared to controls. The results were supported by using the IHC fluorescent antibody staining intensity morphometric quantitation. Morphometric quantification of fluorescent intensity measurement showed a two fold increase in SYK protein in the cytoplasm of the cells forming MDBs compared to surrounding normal hepatocytes. The expression of AKT1 was also analyzed. AKT1 is a serine/threonine-specific protein kinase that plays a key role in multiple cellular processes such as glucose metabolism, apoptosis, cell proliferation, transcription and cell migration. The AKT protein was also increased in hepatocyte balloon cells forming MDBs. This observation demonstrates the role of SYK and its subsequent effect on the internal signaling pathways such as PI3K/AKT as well as p70S6K, as a potential multifunctional target in protein quality control mechanisms of hepatocytes when ER stress is activated.

摘要

在本研究中,使用了来自酒精性肝炎(AH)患者的经福尔马林固定并石蜡包埋(FFPE)的肝活检切片。结果显示,与对照组相比,通过RNA测序和实时PCR分析,酒精性肝炎患者中SYK蛋白的表达上调。使用免疫组化荧光抗体染色强度形态计量定量法也支持了该结果。荧光强度测量的形态计量定量显示,与周围正常肝细胞相比,形成MDBs的细胞胞质中SYK蛋白增加了两倍。还分析了AKT1的表达。AKT1是一种丝氨酸/苏氨酸特异性蛋白激酶,在多种细胞过程中起关键作用,如葡萄糖代谢、细胞凋亡、细胞增殖、转录和细胞迁移。在形成MDBs的肝细胞气球样细胞中,AKT蛋白也增加。这一观察结果证明了SYK的作用及其对PI3K/AKT以及p70S6K等内部信号通路的后续影响,这是内质网应激激活时肝细胞蛋白质质量控制机制中一个潜在的多功能靶点。

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