Literature DB >> 8800748

Human alpha 1-antitrypsin gene transfer to in vivo mouse hepatocytes.

S F Aliño1, M Bobadilla, J Crespo, M Lejarreta.   

Abstract

The in vivo gene transfer to mouse hepatocytes of pTG 7101, a plasmid containing the full-length gene encoding human alpha 1-antitrypsin (alpha 1-AT) DNA, has been studied by iv administration of recombinant DNA (100 ng/mouse) encapsulated in large and small liposomes. Our results from immunohistochemical liver sections and cytophotometric analysis of hepatocyte chromophore absorbance indicate that human alpha 1-AT was expressed in liver parenchymal cells from mice treated (48 hr before) with DNA encapsulated in small liposomes, and this effect remained for at least 2 weeks. In contrast, the efficiency was greatly limited when large liposomes were used as a vehicle for gene transfer. Additional experiments were performed to study using an ELISA procedure the presence in mouse plasma of human alpha 1-AT from mice treated with encapsulated plasmid in small liposomes or small empty liposomes plus free DNA. According to the immunohistochemical data, the results indicate that detectable alpha 1-AT can only be observed in plasma from mice treated with encapsulated plasmid in small liposomes.

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Year:  1996        PMID: 8800748     DOI: 10.1089/hum.1996.7.4-531

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  6 in total

Review 1.  Progress with Recombinant Adeno-Associated Virus Vectors for Gene Therapy of Alpha-1 Antitrypsin Deficiency.

Authors:  Alisha M Gruntman; Terence R Flotte
Journal:  Hum Gene Ther Methods       Date:  2015-06       Impact factor: 2.396

2.  Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy.

Authors:  L W Lai; D M Chan; R P Erickson; S J Hsu; Y H Lien
Journal:  J Clin Invest       Date:  1998-04-01       Impact factor: 14.808

Review 3.  Gene Therapy for Alpha-1 Antitrypsin Deficiency Lung Disease.

Authors:  Maria J Chiuchiolo; Ronald G Crystal
Journal:  Ann Am Thorac Soc       Date:  2016-08

4.  5 Year Expression and Neutrophil Defect Repair after Gene Therapy in Alpha-1 Antitrypsin Deficiency.

Authors:  Christian Mueller; Gwladys Gernoux; Alisha M Gruntman; Florie Borel; Emer P Reeves; Roberto Calcedo; Farshid N Rouhani; Anthony Yachnis; Margaret Humphries; Martha Campbell-Thompson; Louis Messina; Jeffrey D Chulay; Bruce Trapnell; James M Wilson; Noel G McElvaney; Terence R Flotte
Journal:  Mol Ther       Date:  2017-04-10       Impact factor: 11.454

Review 5.  Translational Advances of Hydrofection by Hydrodynamic Injection.

Authors:  Luis Sendra; María José Herrero; Salvador F Aliño
Journal:  Genes (Basel)       Date:  2018-03-01       Impact factor: 4.096

6.  Physico-chemical characteristics of lipoplexes influence cell uptake mechanisms and transfection efficacy.

Authors:  Sarah Resina; Paul Prevot; Alain R Thierry
Journal:  PLoS One       Date:  2009-06-26       Impact factor: 3.240

  6 in total

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