Osteoprotegerin Is more than a Possible Serum Marker in Liver Fibrosis: A Study into Its Function in Human and Murine LiverAdhyatmika, A., Beljaars, L., Putri, K. S. S., Habibie, H., Boorsma, C. E., Reker-Smit, C., Luangmonkong, T., Guney, B., Haak, A., Mangnus, K. A., Post, E., Poelstra, K., Ravnskjaer, K., Olinga, P. & Melgert, B. N., May-2020, In : Pharmaceutics. 12, 5, 21 p., 471.
Research output: Contribution to journal › Article › Academic › peer-review
Osteoprotegerin (OPG) serum levels are associated with liver fibrogenesis and have been proposed as a biomarker for diagnosis. However, the source and role of OPG in liver fibrosis are unknown, as is the question of whether OPG expression responds to treatment. Therefore, we aimed to elucidate the fibrotic regulation of OPG production and its possible function in human and mouse livers. OPG levels were significantly higher in lysates of human and mouse fibrotic livers compared to healthy livers. Hepatic OPG expression localized in cirrhotic collagenous bands in and around myofibroblasts. Single cell sequencing of murine liver cells showed hepatic stellate cells (HSC) to be the main producers of OPG in healthy livers. Using mouse precision-cut liver slices, we found OPG production induced by transforming growth factor beta 1 (TGF beta 1) stimulation. Moreover, OPG itself stimulated expression of genes associated with fibrogenesis in liver slices through TGF beta 1, suggesting profibrotic activity of OPG. Resolution of fibrosis in mice was associated with decreased production of OPG compared to ongoing fibrosis. OPG may stimulate fibrogenesis through TGF beta 1 and is associated with the degree of fibrogenesis. It should therefore be investigated further as a possible drug target for liver fibrosis or biomarker for treatment success of novel antifibrotics.
|Number of pages||21|
|Publication status||Published - May-2020|
- cirrhosis, TGF beta 1, CCl4, resolution, hepatic stellate cells, osteoprotegerin, RANKL, TRAIL, PRECISION-CUT LIVER, RECEPTOR ACTIVATOR, CELLS, FIBROGENESIS, EXPRESSION, APOPTOSIS, SLICES, LIGAND, VIVO