Stem cell factor restores hepatocyte proliferation in IL-6 knockout mice following 70% hepatectomy
Open accessAbstract
Stem cell factor (SCF) is a molecule with known proliferative effects on hematopoietic cells. More recent studies suggest that this molecule may also have effects on cellular differentiation and proliferation in other types of cells. The current investigations demonstrate that there is a large reservoir of SCF in the liver, that hepatic SCF levels change dramatically following partial hepatectomy in mice, and that SCF blockade, either by administration of anti-SCF antibodies or by using genetically altered, SCF-deficient mice, inhibits hepatocyte proliferation after partial hepatectomy; if SCF is replaced in the genetically SCF-deficient mice after partial hepatectomy, hepatocyte proliferation is restored to that seen in WT animals. Furthermore, SCF administration to IL-6 knockout mice also restores hepatocyte proliferation to normal. In vitro studies using primary mouse hepatocytes demonstrate that SCF causes hepatocyte proliferation and is induced by IL-6 and that treatment with anti-SCF antibodies inhibits IL-6-induced hepatocyte proliferation. Further in vivo studies in IL-6 knockout mice demonstrate that SCF administration to these animals increases p-stat3 levels, suggesting that the SCF-induced increase in hepatocyte proliferation in this system is stat3-mediated.
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Liver-specific deletion of Yap or Yap and Taz significantly blunts liver weight restoration after PHx, similar to IL-6-knockout mice.
“Mice with liver-specific deletion of Yap or Yap and Taz suffer significantly blunted liver weight restoration after PHx (55, 56), similar to IL-6–knockout mice (39).”
From Senescent hepatic stellate cells promote liver regeneration through IL-6 and ligands of CXCR2 (2022) · cites this paper as [39]
IL-6 is known to regulate hepatocyte proliferation, and IL-6-knockout mice have impaired liver regeneration.
“IL-6 is known to regulate hepatocyte proliferation, and IL-6–knockout mice have impaired liver regeneration (38, 39).”
From Senescent hepatic stellate cells promote liver regeneration through IL-6 and ligands of CXCR2 (2022) · cites this paper as [39]
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Liver Failure and Defective Hepatocyte Regeneration in Interleukin-6-Deficient Mice
Cressman, D. E., Greenbaum, L. E., DeAngelis, R. A., Ciliberto, G., Furth, E. E., Poli, V., & Taub, R. (1996) · Science · doi:10.1126/science.274.5291.1379 · Cited by 1,536 · see citing works
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- Glantz, S.A. 1987. Alternatives to analysis of variance and the t test based on ranks. In Primer of biostatistics. S.A. Glantz, editor. McGraw-Hill. New York, New York, USA. 287-331.
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Senescent hepatic stellate cells promote liver regeneration through IL-6 and ligands of CXCR2
Cheng, N., Kim, K.-H., & Lau, L. F. (2022) · JCI Insight · doi:10.1172/jci.insight.158207 · Cited by 87 · see citing works
“Mice with liver-specific deletion of Yap or Yap and Taz suffer significantly blunted liver weight restoration after PHx (55, 56), similar to IL-6–knockout mice (39).”
da Silva, C. G., Studer, P., Skroch, M., Mahiou, J., Minussi, D. C., Peterson, C. R., Wilson, S. W., Patel, V. I., Ma, A., Csizmadia, E., et al. (2013) · Hepatology · doi:10.1002/hep.26197 · Cited by 77 · see citing works
- Authors
- Ren, X., Hogaboam, C., Carpenter, A., & Colletti, L.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Colletti, Lisa
- ORCID
- Hogaboam, Cory
- Venue
- Journal of Clinical Investigation
- Published
- 2003-11-01
- Volume
- 112
- Issue
- 9
- Pages
- 1407-1418
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC228393
- OpenAlex
- W2149130539
- Cited by
- 80
- References
- 1
- Citations by year
- 2025: 1 · 2023: 1 · 2022: 3 · 2021: 5 · 2020: 3 · 2018: 1 · 2017: 6 · 2016: 2 · 2015: 1 · 2014: 4 · 2013: 3 · 2012: 5
- FWCI
- 3.71
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK53224, R01 DK-58106, R01DK053224, R01DK058106)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Keywords
- stem cell factor, hepatocyte proliferation, partial hepatectomy, interleukin-6, IL-6 knockout mice, STAT3 signaling, liver, hepatocyte regeneration
- MeSH terms
- Animals, Bromodeoxyuridine, Cell Division, DNA-Binding Proteins, Hepatectomy, Male, Mice, Inbred CBA, Trans-Activators, Interleukin-6, Mice, Knockout, Stem Cell Factor, Hepatocytes, STAT3 Transcription Factor, Mice
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