In this work, the authors used the ΦC31 integrase system to study the effects of the continuous exposure of exogenous sclerostin on bone. They injected Sost-attB plasmid with ΦC31 integrase plasmid into the mouse tail vein using a hydrodynamic-based method. Sclerostin was expressed in the hepatocytes, secreted into the blood flow, and maintained at high concentrations in the mice injected. These mice showed trabecular bone loss on micro-CT analysis. These findings may help to further ascertain the effects of sclerostin introduced exogenously on the skeleton.
This introduction video shows how the choice of every vector element can modify the lentiviral vector's activity.
BigField GEG Tech's insight:
Video which explains the influence of promoter, integrase or envelope on the activity of lentiviral vectors. The goal is to design the best vector according to the experimental needs.
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In this work, the authors used the ΦC31 integrase system to study the effects of the continuous exposure of exogenous sclerostin on bone. They injected Sost-attB plasmid with ΦC31 integrase plasmid into the mouse tail vein using a hydrodynamic-based method. Sclerostin was expressed in the hepatocytes, secreted into the blood flow, and maintained at high concentrations in the mice injected. These mice showed trabecular bone loss on micro-CT analysis. These findings may help to further ascertain the effects of sclerostin introduced exogenously on the skeleton.