1997
DOI: 10.1016/s0304-4165(96)00125-0
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Augmented inhibitory effect of superoxide dismutase on superoxide anion release from macrophages by direct cationization

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Cited by 9 publications
(2 citation statements)
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“…Since Felgner (8) reported efficient gene expression using cationic lipids for the transfection of cells with plasmid DNA, cationic molecule-based delivery systems for plasmid DNA have been extensively investigated in an attempt to achieve nonviral gene transfer to target cells (33). In addition, enzymes such as SOD (27,28,40,48), glucose oxidase (21), and catalase (21,43), as well as serum albumins (32), immunoglobulins (52), and ferritin (7), all of which are negatively charged at physiological pH, have been directly modified with diamines to obtain cationized derivatives. Cationized proteins exhibit increased cellular uptake by brain microvascular endothelial cells, hepatocytes, kidney epithelial cells, and enterocytes.…”
Section: Discussionmentioning
confidence: 99%
“…Since Felgner (8) reported efficient gene expression using cationic lipids for the transfection of cells with plasmid DNA, cationic molecule-based delivery systems for plasmid DNA have been extensively investigated in an attempt to achieve nonviral gene transfer to target cells (33). In addition, enzymes such as SOD (27,28,40,48), glucose oxidase (21), and catalase (21,43), as well as serum albumins (32), immunoglobulins (52), and ferritin (7), all of which are negatively charged at physiological pH, have been directly modified with diamines to obtain cationized derivatives. Cationized proteins exhibit increased cellular uptake by brain microvascular endothelial cells, hepatocytes, kidney epithelial cells, and enterocytes.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, the potential utility of Ad35 vectors as vaccine vectors has been proposed, 29,30 and DC and macrophages are considered to be ideal targets for immunotherapy using Ad35 vector-based vaccines. Bone marrow-derived dendritic cells 31 and peritoneal macrophages 32 were prepared as Figure 1 Human CD46 expression in organs harvested from CD46TG mice. The protein samples were prepared from wild-type mice (0n), hemizygous CD46TG mice (1n) and homozygous CD46TG mice (2n).…”
mentioning
confidence: 99%