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Vol. 297, Issue 3, 853-860, June 2001
Departments of Biopharmaceutics and Drug Metabolism (N.K., T.K.,
K.Y., Y.T.) and Drug Delivery Research (M.H.), Graduate School of
Pharmaceutical Sciences, Kyoto University, Kyoto, Japan
Hepatic uptake and gene expression mechanisms following intravenous
administration of naked plasmid DNA (pDNA) by conventional and
hydrodynamics-based procedures were studied in mice. After conventional
(normal) intravenous injection, 32P-labeled pDNA was
rapidly eliminated from the circulation and predominantly taken up by
the liver nonparenchymal cells while no significant gene expression was
observed in this organ. The hepatic uptake process was saturable.
Involvement of a specific mechanism was demonstrated since the hepatic
uptake of [32P]pDNA was dramatically inhibited by cold
pDNA, calf thymus DNA, and some polyanions [polyinosinic acid (poly
I), dextran sulfate], but not by others (polycytidylic acid,
chondroitin sulfate). The liver endothelial cells appeared to be a
major contributor because gadolinium chloride
(GdCl3)-induced Kupffer cell blockade did not affect the
hepatic uptake. After intravenous injection of naked pDNA with a large
volume of saline at a high velocity (hydrodynamics-based procedure),
the apparent hepatic uptake profile was similar to that after normal
injection. The hepatic uptake was not inhibited by prior administration
of polyanions, including poly I, dextran sulfate, and heparin. The
hydrodynamics-based procedure resulted in marked gene expression in the
liver, which was not inhibited by prior administration of polyanions or
GdCl3 treatment. These results indicate that pDNA uptake is
a nonspecific process. This hypothesis was supported by the finding
that significant hepatic uptake of bovine serum albumin and
immunoglobulin G was observed after the hydrodynamics-based procedure.
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