Interleukin-6 from intrahepatic cells of bone marrow origin is required for normal murine liver regeneration
Open Access
- 1 January 2002
- journal article
- Published by Wolters Kluwer Health in Hepatology
- Vol. 35 (1) , 40-48
- https://doi.org/10.1053/jhep.2002.30081
Abstract
Interleukin-6 (IL-6) is required for normal liver regeneration, but the specific cellular source of this growth factor is unknown. We investigated whether this signal originates from the resident macrophage, the Kupffer cell. Using a murine model of bone marrow transplantation, we replaced recipient bone marrow-derived cells, including Kupffer cells, with cells of donor genetic phenotype. Recipients deficient in IL-6 (IL-6−/−) were lethally irradiated, then rescued with 107 donor bone marrow cells capable of expressing IL-6 (IL-6+/+). Conversely, IL-6+/+ recipients received IL-6−/− marrow. Successful engraftment was measured by the presence of the Y chromosome SRY locus in the livers of female recipients receiving male marrow, in situ IL-6 expression by Kupffer cells, and up-regulation of IL-6 in splenocytes after activation with lipopolysaccharide (LPS). Kupffer cell isolation in IL-6−/− females receiving IL-6+/+ male marrow clearly showed the presence of the SRY locus and IL-6 disrupted allele, whereas males receiving female marrow demonstrated no SRY or IL-6 signals, confirming the extent of replacement. Replacement of these cells in IL-6−/− mice with IL-6+/+ bone marrow successfully restored the regenerative response after partial hepatectomy (PHx) as indicated by signal transduction and activator of transcription 3 (STAT3) activation and hepatocyte DNA replication. Alternatively, complete replacement of Kupffer cells in IL-6+/+ mice by transplantation with IL-6−/− cells significantly inhibited liver regeneration and was partially restored by administration of IL-6. This investigation demonstrates a paracrine mechanism by which cells of bone marrow origin, most likely Kupffer cells, regulate the regenerative capacity of the hepatocyte through IL-6 expression.Keywords
Funding Information
- National Institute of Health Center (P30 DK50306)
- Fred and Suzanne Biesecker Center for Pediatric Liver Disease at the Children' Hospital of Philadelphia
This publication has 28 references indexed in Scilit:
- NADPH oxidase–derived free radicals are key oxidants in alcohol-induced liver diseaseJournal of Clinical Investigation, 2000
- Interleukin 6 and liver regenerationGut, 2000
- Increased toxin-induced liver injury and fibrosis in interleukin-6-deficient miceHepatology, 2000
- DIFFERENTIALLY INCREASED IL-6 mRNA EXPRESSION IN LIVER AND SPLEEN FOLLOWING INJECTION OF LIPOSOME-ENCAPSULATED HAEMOGLOBINCytokine, 1999
- Mitosis and Apoptosis in the Liver of Interleukin–6-Deficient Mice After Partial HepatectomyHepatology, 1999
- Transcriptional Regulatory Signals Define Cytokine-Dependent and -Independent Pathways in Liver RegenerationSeminars in Liver Disease, 1999
- Role of Cytokines and Cytokine-Producing Cells in Reperfusion Injury to the LiverSeminars in Liver Disease, 1999
- Liver Failure and Defective Hepatocyte Regeneration in Interleukin-6-Deficient MiceScience, 1996
- Destruction of Kupffer cells increases survival and reduces graft injury after transplantation of fatty livers from ethanol-treated ratsLiver Transplantation and Surgery, 1996
- Review: Regulation of liver regeneration by pro‐inflammatory cytokinesJournal of Gastroenterology and Hepatology, 1996