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肝细胞大小分级分离可用于解析人类肝脏的分区。

Hepatocyte size fractionation allows dissection of human liver zonation.

机构信息

Department of Pharmacy, Uppsala University, Uppsala, Sweden.

DMPK, Research and Early Development Cardiovascular Renal and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.

出版信息

J Cell Physiol. 2021 Aug;236(8):5885-5894. doi: 10.1002/jcp.30273. Epub 2021 Jan 16.

DOI:10.1002/jcp.30273
PMID:33452735
Abstract

Human hepatocytes show marked differences in cell size, gene expression, and function throughout the liver lobules, an arrangement termed liver zonation. However, it is not clear if these zonal size differences, and the associated phenotypic differences, are retained in isolated human hepatocytes, the "gold standard" for in vitro studies of human liver function. Here, we therefore explored size differences among isolated human hepatocytes and investigated whether separation by size can be used to study liver zonation in vitro. We used counterflow centrifugal elutriation to separate cells into different size fractions and analyzed them with label-free quantitative proteomics, which revealed an enrichment of 151 and 758 proteins (out of 5163) in small and large hepatocytes, respectively. Further analysis showed that protein abundances in different hepatocyte size fractions recapitulated the in vivo expression patterns of previously described zonal markers and biological processes. We also found that the expression of zone-specific cytochrome P450 enzymes correlated with their metabolic activity in the different fractions. In summary, our results show that differences in hepatocyte size matches zonal expression patterns, and that our size fractionation approach can be used to study zone-specific liver functions in vitro.

摘要

人肝细胞在整个肝小叶中表现出明显的细胞大小、基因表达和功能差异,这种排列方式被称为肝区带化。然而,目前尚不清楚这些区带大小的差异以及相关的表型差异是否在分离的人原代肝细胞中保留,因为后者是研究人类肝脏功能的体外研究的“金标准”。在这里,我们因此探索了分离的人原代肝细胞之间的大小差异,并研究了是否可以通过大小分离来研究体外的肝区带化。我们使用逆流离心淘洗法将细胞分离成不同大小的分数,并使用无标记定量蛋白质组学进行分析,结果显示,在小肝细胞和大肝细胞中分别分别富集了 151 和 758 种蛋白质(5163 种中的)。进一步的分析表明,不同肝细胞大小分数中的蛋白质丰度重现了先前描述的区带标志物和生物学过程的体内表达模式。我们还发现,特定区带细胞色素 P450 酶的表达与其在不同分数中的代谢活性相关。总之,我们的研究结果表明,肝细胞大小的差异与区带表达模式相匹配,并且我们的大小分级分离方法可用于体外研究特定区带的肝脏功能。

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