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Ramackers, W; Klose, J; Vondran, FW; Schrem, H; Kaltenborn, A; Klempnauer, J; Kleine, M.
Species-specific regulation of fibrinogen synthesis with implications for porcine hepatocyte xenotransplantation.
Xenotransplantation. 2014; 21(5): 444-453. Doi: 10.1111/xen.12110
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Co-authors Med Uni Graz
Schrem Harald Heinrich
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Abstract:
Patients with liver failure could potentially be bridged with porcine xenogeneic liver cell transplantation. We examined species-specific differences between primary human and porcine hepatocytes in the regulation of coagulation protein expression and function. Isolated primary human and porcine hepatocytes were stimulated with either porcine or human interleukin (IL)-6 (10 ng/ml), IL-1β (10 ng/ml), and tumor necrosis factor-alpha (TNF-α, 30 ng/ml). mRNA expression of coagulation factors were measured by RT-PCR and real-time PCR. Cell culture supernatants were used for the measurement of fibrinogen by ELISA and determination of fibrin clot generation. Fibrinogen expression in human hepatocytes increased after IL-6 treatment (P = 0.010) and decreased after TNF-α treatment (P = 0.005). Porcine hepatocytes displayed a lower increase in fibrinogen expression after IL-6 treatment as compared to hepatocytes of human origin (P = 0.021). Porcine hepatocytes responded contrarily following TNF-α treatment with an increased expression of fibrinogen resulting in a significant species-specific difference between human and porcine hepatocytes (P = 0.029). Fibrin polymer generation by human hepatocytes was stable and widely branched after IL-6 treatment, while stimulation with TNF-α displayed no fibrin generation at all. In contrast, treatment of porcine hepatocytes with TNF-α resulted in generation of a stable and widely branched fibrin polymer, and stimulation with IL-6 only leads to generation of partial fibrin aggregates. We identified species-specific differences in the regulation of fibrinogen mRNA expression and fibrin generation under inflammatory stimuli. In hepatic xenotransplantation of porcine origin, these interspecies differences might lead to a loss of physiological coagulation function and a loss of transplanted cells. © 2014 John Wiley & Sons A/S Published by John Wiley & Sons Ltd.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Biomarkers - metabolism
Enzyme-Linked Immunosorbent Assay -
Fibrinogen - metabolism
Hepatocytes - metabolism
Hepatocytes - transplantation
Humans -
Interleukin-1beta - metabolism
Interleukin-6 - metabolism
Real-Time Polymerase Chain Reaction -
Reverse Transcriptase Polymerase Chain Reaction -
Swine -
Transplantation, Heterologous - methods
Tumor Necrosis Factor-alpha - metabolism

Find related publications in this database (Keywords)
acute phase reaction
hepatocyte transplantation
human cytokines
IL-1 beta
IL-6
species-specific gene regulation
TNF-alpha
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