Pregnane X receptor is essential for normal progression of liver regeneration†
Abstract
Unlabelled Pregnane X receptor (PXR) mediates xenobiotic and endobiotic metabolism as well as hepatocyte proliferation. To determine the role of PXR in liver regeneration, 2/3 partial hepatectomy (PH) was performed on wild-type and PXR-null mice. Our results showed that hepatic steatosis was markedly suppressed in mice lacking PXR 36 hours after PH, concomitant with reduction of hepatocyte proliferation at the same time point. Gene expression analysis revealed the role of PXR in regulating the transcription of genes involved in lipid uptake, transport, biosynthesis, oxidation, and storage during liver regeneration. When PXR was absent, the second wave of hepatocyte proliferation was severely suppressed, which was accompanied by the inactivation of STAT3. Lack of PXR inhibited the second phase of liver growth, leading to 17% less liver mass at the anticipated end point of liver regeneration (day 10). Conclusion PXR is required for normal progression of liver regeneration by modulating lipid homeostasis and regulating hepatocyte proliferation.
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PXR can accelerate regeneration.
“PXR can accelerate regeneration,57, 58, 59”
From Constitutive Androstane Receptor Regulates Bile Acid Homeostasis and Metabolism During Liver Regeneration (2026) · cites this paper as [57]
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References 53 · Cited by 114
- Authors
- Dai, G., He, L., Bu, P., & Wan, Y. Y.
- Affiliations
- University of Kansas Medical Center (US)
- Corresponding author
- Wan, Yu‐Jui Yvonne
- Venue
- Hepatology
- Published
- 2008-04
- Volume
- 47
- Issue
- 4
- Pages
- 1277-1287
- ISSN
- 0270-9139 (ISSN-L)
- OpenAlex
- W2076100042
- Cited by
- 114
- References
- 53
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 7 · 2020: 3 · 2019: 2 · 2018: 6 · 2017: 5 · 2016: 3 · 2015: 11 · 2014: 12 · 2013: 7 · 2012: 5
- FWCI
- 6.80
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Hepatology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5p20rr015563-08)
- National Institute on Alcohol Abuse and Alcoholism (AA 14147, R01AA014147)
- National Cancer Institute (R01CA053596, CA-53596)
- National Center for Research Resources (P20-RR015563, P20RR021940, P20RR016475)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Health Sciences › Medicine › Surgery › Organ Transplantation Techniques and Outcomes
- Keywords
- pregnane X receptor, liver regeneration, partial hepatectomy, hepatocyte proliferation, hepatic steatosis, lipid homeostasis, STAT3, lipid metabolism
- MeSH terms
- Pregnane X Receptor, Animals, Hepatectomy, Homeostasis, Liver, Liver Regeneration, Male, Membrane Proteins, Mice, Inbred C57BL, Receptors, Steroid, RNA, Messenger, Gene Expression, Mice, Knockout, Hepatocytes, Cell Proliferation, Lipid Metabolism, STAT3 Transcription Factor, Mice, Cytochrome P-450 CYP3A
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