硫氧化物9
胆管上皮细胞
肝损伤
再生(生物学)
肝再生
睾丸决定因素
肝细胞
生物
人肝
胆管
表型
内科学
细胞生物学
内分泌学
医学
体外
转录因子
基因
遗传学
Y染色体
作者
Yuji Suzuki,Teruo Sasaki,Keisuke Kakisaka,Hiroaki Abe,Yasuhiro Takikawa
出处
期刊:Springer eBooks
[Springer Nature]
日期:2022-01-01
卷期号:: 217-225
被引量:1
标识
DOI:10.1007/978-1-0716-2557-6_16
摘要
AbstractThe liver has a remarkable regenerative capacity with different modes of regeneration according to the type and extent of an injury. It has been reported that mature hepatocytes could transdifferentiate into a cholangiocyte phenotype. Sry HMG box protein 9 (SOX9) is one of the earliest biliary markers that regulate bile duct development. We have found that SOX9-positive biphenotypic hepatocytes appear in severe acute liver injury patients’ liver specimens accompanied by an elevation in plasma interleukin-8 levels. In vitro assays revealed that interleukin-8 homologs induce the expression of SOX9 in mature mouse hepatocytes. Here, we describe the methods used to detect SOX9-positive hepatocytes in human liver specimens and to induce SOX9-positive hepatocytes in mature mouse hepatocytes.Key wordsInterleukin-8Sry HMG box protein 9Mature hepatocyteTransdifferentiationLiver regeneration
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