4.7 Article

Pregnane X receptor promotes liver enlargement in mice through the spatial induction of hepatocyte hypertrophy and proliferation

期刊

CHEMICO-BIOLOGICAL INTERACTIONS
卷 367, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2022.110133

关键词

Pregnane X receptor; Hepatomegaly; Hepatocyte hypertrophy; Hepatocyte proliferation

资金

  1. Natural Science Foundation of China
  2. National Key Research and Development Program
  3. Shenzhen Science and Technology Program
  4. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program
  5. National Engineering and Technology Research Center for New drug Druggability Evaluation
  6. [82025034]
  7. [81973392]
  8. [82000593]
  9. [2017YFE0109900]
  10. [KQTD20190929174023858]
  11. [2017BT01Y093]
  12. [2017B090903004]

向作者/读者索取更多资源

This study aimed to explore the features of spatial changes in hepatocytes during PXR-induced liver enlargement. The results showed that hepatocyte hypertrophy mainly occurred around the central vein, while hepatocyte proliferation mainly occurred around the portal vein. Furthermore, the spatial changes in hepatocyte hypertrophy and proliferation were closely associated with the regional expression of related proteins and the regional distribution of triglycerides.
Nuclear receptor pregnane X receptor (PXR) can induce significant liver enlargement through hepatocyte hy-pertrophy and proliferation. A previous report showed that during the process of PXR-induced liver enlargement, hepatocyte hypertrophy occurs around the central vein (CV) area while hepatocyte proliferation occurs around the portal vein (PV) area. However, the features of this spatial change remain unclear. Therefore, this study aims to explore the features of the spatial changes in hepatocytes in PXR-induced liver enlargement. PXR-induced spatial changes in hepatocyte hypertrophy and proliferation were confirmed in C57BL/6 mice. The liver was perfused with digitonin to destroy the hepatocytes around the CV or PV areas, and then the regional expression of proteins related to hepatocyte hypertrophy and proliferation was further measured. The results showed that the expression of PXR downstream proteins, such as cytochrome P450 (CYP) 3A11, CYP2B10, P-glycoprotein (P-gp) and organ anion transporting polypeptide 4 (OATP4) was upregulated around the CV area, while the expression of proliferation-related proteins such as cyclin B1 (CCNB1), cyclin D1 (CCND1) and serine/threonine NIMA-related kinase 2 (NEK2) was upregulated around the PV area. At the same time, the expression of cyclin-dependent kinase inhibitors such as retinoblastoma-like protein 2 (RBL2), cyclin-dependent kinase inhibitor 1B (CDKN1B) and CDKN1A was downregulated around the PV area. This study demonstrated that the spatial change in PXR-induced hepatocyte hypertrophy and proliferation is associated with the regional expression of PXR downstream targets and proliferation-related proteins and the regional distribution of triglycerides (TGs). These findings provide new insight into the understanding of PXR-induced hepatomegaly.

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