Literature DB >> 12072532

Evaluation of Tat-encoding bicistronic human immunodeficiency virus type 1 gene transfer vectors in primary canine bone marrow mononuclear cells.

Narasimhachar Srinivasakumar1, Michail Zaboikin, Tatiana Zaboikina, Friedrich Schuening.   

Abstract

Tat-encoding human immunodeficiency virus type 1 (HIV-1) gene transfer vectors were evaluated in primary canine bone marrow mononuclear cells. Tat vectors provided higher levels of gene expression than vectors with internal promoters. The HIV-1 vector was also more efficient than Moloney murine leukemia virus (MoMLV) vectors for transduction of canine bone marrow mononuclear cells in vitro. Transplantation experiments in dogs with transduced autologous marrow cells confirmed the superiority of HIV-1 vectors over MoMLV vectors for gene transfer into canine bone marrow cells. Tat vectors may be useful not only for providing high levels of therapeutic gene expression in hematopoietic cells but also for study of the biological effects of Tat in those tissues in the canine model.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12072532      PMCID: PMC136335          DOI: 10.1128/jvi.76.14.7334-7342.2002

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  36 in total

1.  HIV-1 genome nuclear import is mediated by a central DNA flap.

Authors:  V Zennou; C Petit; D Guetard; U Nerhbass; L Montagnier; P Charneau
Journal:  Cell       Date:  2000-04-14       Impact factor: 41.582

2.  High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors.

Authors:  P Salmon; V Kindler; O Ducrey; B Chapuis; R H Zubler; D Trono
Journal:  Blood       Date:  2000-11-15       Impact factor: 22.113

3.  Human immunodeficiency virus type 1 vpr induces apoptosis through caspase activation.

Authors:  S A Stewart; B Poon; J Y Song; I S Chen
Journal:  J Virol       Date:  2000-04       Impact factor: 5.103

4.  Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cells.

Authors:  D S An; R P Wersto; B A Agricola; M E Metzger; S Lu; R G Amado; I S Chen; R E Donahue
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

5.  Induction of cytotoxic T lymphocyte and antibody responses to enhanced green fluorescent protein following transplantation of transduced CD34(+) hematopoietic cells.

Authors:  M Rosenzweig; M Connole; R Glickman; S P Yue; B Noren; M DeMaria; R P Johnson
Journal:  Blood       Date:  2001-04-01       Impact factor: 22.113

6.  Lentivirus vector-mediated hematopoietic stem cell gene transfer of common gamma-chain cytokine receptor in rhesus macaques.

Authors:  D S An; S K Kung; A Bonifacino; R P Wersto; M E Metzger; B A Agricola; S H Mao; I S Chen; R E Donahue
Journal:  J Virol       Date:  2001-04       Impact factor: 5.103

7.  The human immunodeficiency virus type-1 central DNA flap is a crucial determinant for lentiviral vector nuclear import and gene transduction of human hematopoietic stem cells.

Authors:  A Sirven; F Pflumio; V Zennou; M Titeux; W Vainchenker; L Coulombel; A Dubart-Kupperschmitt; P Charneau
Journal:  Blood       Date:  2000-12-15       Impact factor: 22.113

8.  Novel Tat-encoding bicistronic human immunodeficiency virus type 1-based gene transfer vectors for high-level transgene expression.

Authors:  N Srinivasakumar; F Schuening
Journal:  J Virol       Date:  2000-07       Impact factor: 5.103

9.  Lentiviral delivery of HIV-1 Vpr protein induces apoptosis in transformed cells.

Authors:  S A Stewart; B Poon; J B Jowett; Y Xie; I S Chen
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

10.  Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences.

Authors:  A Follenzi; L E Ailles; S Bakovic; M Geuna; L Naldini
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

View more
  2 in total

1.  Rev-free HIV-1 gene delivery system for targeting Rev-RRE-Crm1 nucleocytoplasmic RNA transport pathway.

Authors:  Narasimhachar Srinivasakumar
Journal:  PLoS One       Date:  2011-12-02       Impact factor: 3.240

2.  Substitution of the Rev-response element in an HIV-1-based gene delivery system with that of SIVmac239 allows efficient delivery of Rev M10 into T-lymphocytes.

Authors:  Narasimhachar Srinivasakumar
Journal:  AIDS Res Ther       Date:  2008-06-05       Impact factor: 2.250

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.