A comparison between intravenous and peritoneal route on liver targeted uptake and expression of plasmid delivered by Glyco-poly-l-lysine.

AIM:To compare the effects of intravenous route and peritoneal route on liver targeted uptake and expression of plasmid delivered by galactose-terminal glyco-poly-l-lysine (G-PLL).METHODS:The plasmid pTM/MMP-1 which could be expressed in eukaryotic cells was bound to G-PLL, and was then transferred into Wistar rats by intravenous and intraperitoneal injection. The expression and distribution of the plasmid were observed at different time periods by in situ hybridization and immunohistochemistry.RESULTS:The plasmid could be expressed significantly within 24 h after being transferred in vivo by both intravenous and intraperitoneal routes. One week later the expression began to decrease, and could still be observed three weeks later. Although both the intravenous and intraperitoneal route could target-specifically deliver the plasmid to the liver, the effect of the former was better as compared to that of the latter.CONCLUSION:Intravenous route is better for liver targeted uptake and expression of G-PLL-bound plasmids than the peritoneal route.

[1]  Catherine H. Wu,et al.  A DNA delivery system containing listeriolysin O results in enhanced hepatocyte-directed gene expression. , 1999, World journal of gastroenterology.

[2]  B. Darimont The Hsp90 chaperone complex A potential target for cancer therapy? , 1999, World journal of gastroenterology.

[3]  A. Gasbarrini,et al.  Gene therapy for human liver diseases. , 1999, European journal of gastroenterology & hepatology.

[4]  P. Zhou,et al.  Antisense to cyclin D1 reverses the transformed phenotype of human gastric cancer cells. , 1999, World journal of gastroenterology.

[5]  Zhirong Zhang,et al.  Study on liver targeting and hepatocytes permeable valaciclovir polybutylcyanoacrylate nanoparticles. , 1999, World Journal of Gastroenterology.

[6]  Wenge Zhang,et al.  Retrovirus-ediated antisense RNA to bcl-2 alter the biological behavior of stomach carcinoma MGC-03 cell lines , 1998 .

[7]  Catherine H. Wu,et al.  Gene therapy and liver diseases , 1998 .

[8]  H. Ren,et al.  Sequencing of PCR amplified HBV DNA pre-c and c regions in the 2.2.15 cells and antiviral action by targeted antisense oligonucleotide directed against sequence. , 1998, World journal of gastroenterology.

[9]  S. Y. Shin,et al.  Detection of the asialoglycoprotein receptor on cell lines of extrahepatic origin. , 1998, Biochemical and biophysical research communications.

[10]  M. Zern,et al.  Increased liver uptake of liposomes and improved targeting efficacy by labeling with asialofetuin in rodents , 1998, Hepatology.

[11]  Shu-nong Li,et al.  CEA and AFP expression in human hepatoma cells transfected with antisense IGF-I gene. , 1998, World journal of gastroenterology.

[12]  U. Losert,et al.  Gene transfer with IL‐4 and IL‐13 improves survival in lethal endotoxemia in the mouse and ameliorates peritoneal macrophages immune competence , 1998, European journal of immunology.

[13]  X. Bing IL 6 expression in transferred NIH3T3 cells by retrovirus vector , 1998 .

[14]  P. D. Cook,et al.  In vivo fate of phosphorothioate antisense oligodeoxynucleotides: predominant uptake by scavenger receptors on endothelial liver cells. , 1997, Nucleic acids research.

[15]  Pla Jinan Specific Delivery To Liver Cells By Asialoglycoprotein Modified Antisence Oligodeo Ynucleotides In Vitro And In Vivo , 1997 .

[16]  L. J. Fisher,et al.  Gene therapy in neurology. , 1996, Current opinion in pediatrics.

[17]  M. Kay,et al.  Adenovirus-mediated hepatic gene transfer in mice: comparison of intravascular and biliary administration. , 1996, Human gene therapy.

[18]  P. Low,et al.  Tumor-selective radiopharmaceutical targeting via receptor-mediated endocytosis of gallium-67-deferoxamine-folate. , 1996, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[19]  M Vapalahti,et al.  [Human gene therapy]. , 1996, Duodecim; laaketieteellinen aikakauskirja.

[20]  Duarte Rg Gene therapy in neurology. State of the art and future prospects , 1995 .

[21]  K. Koike,et al.  Receptor-mediated transfer of pSV2CAT DNA to mouse liver cells using asialofetuin-labeled liposomes. , 1995, Gene therapy.

[22]  H. Klenk,et al.  The asialoglycoprotein receptor is a potential liver-specific receptor for Marburg virus. , 1995, The Journal of general virology.

[23]  R. Duarte [Gene therapy in neurology. State of the art and future prospects]. , 1995, Neurología.

[24]  J. Armendáriz-Borunda,et al.  Nonenzymatic glycosylation of poly‐l‐lysine: A new tool for targeted gene delivery , 1994, Hepatology.

[25]  D. M. Carlson,et al.  Dexamethasone enhancement of gene expression after direct hepatic DNA injection. , 1994, The Journal of biological chemistry.

[26]  F. Stickel,et al.  Demographics of anti-asialoglycoprotein receptor autoantibodies in autoimmune hepatitis. , 1994, Gastroenterology.

[27]  C. Wu,et al.  Overexpression of human methylmalonyl CoA mutase in mice after in vivo gene transfer with asialoglycoprotein/polylysine/DNA complexes. , 1994, Human gene therapy.

[28]  N. Ferry Thérapie génique du foie: du laboratoire au chevet du malade , 1994 .

[29]  S. Russell,et al.  Gene transfer technologies for the gene therapy of cancer. , 1994, Gene therapy.

[30]  M. Yarmush,et al.  Antisense DNA delivery in vivo: liver targeting by receptor-mediated uptake. , 1994, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[31]  N. Ferry [Gene therapy of the liver: from the laboratory to the patient's bedside]. , 1994, Acta gastro-enterologica Belgica.

[32]  L. Dini,et al.  Galactose-specific receptor modulation related to the onset of apoptosis in rat liver. , 1993, European journal of cell biology.

[33]  C. Wu,et al.  Fate of DNA targeted to the liver by asialoglycoprotein receptor-mediated endocytosis in vivo. Prolonged persistence in cytoplasmic vesicles after partial hepatectomy. , 1993, The Journal of biological chemistry.

[34]  D. Alpers,et al.  Asialoglycoprotein receptor mRNAs are expressed in most extrahepatic rat tissues during development. , 1993, American Journal of Physiology.

[35]  D. Meijer,et al.  Hepatic and intrahepatic targeting of an anti-inflammatory agent with human serum albumin and neoglycoproteins as carrier molecules. , 1993, Biochemical pharmacology.

[36]  M. Nakanishi,et al.  Expression of hepatitis B virus surface antigen in adult rat liver. Co-introduction of DNA and nuclear protein by a simplified liposome method. , 1991, The Journal of biological chemistry.

[37]  C. Wu,et al.  Delivery systems for gene therapy , 1991, Biotherapy.

[38]  H. Birkedal‐Hansen,et al.  The cysteine switch: a principle of regulation of metalloproteinase activity with potential applicability to the entire matrix metalloproteinase gene family. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[39]  James M. Wilson,et al.  Targeting genes: delivery and persistent expression of a foreign gene driven by mammalian regulatory elements in vivo. , 1989, The Journal of biological chemistry.