Lentiviral vector-mediated gene transfer to endotherial cells compared with adenoviral and retroviral vectors

Preparative Biochemistry and Biotechnology

Volumn 37, Issue 1, 2007, Pages 1-11

  Sakoda, Tsuyoshi ^a   Kasahara, Nori ^b   Kedes, Larry ^c   Ohyanagi, Mitsumasa ^a  

^a HYOGO COLLEGE OF MEDICINE   (Japan)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

Adenovirus; Endotherial cells; Gene therapy; Lentivirus; Retrovirus

Indexed keywords

ADENOVIRUS; ANIMAL; ARTICLE; CATTLE; COMPARATIVE STUDY; CYTOLOGY; ENDOTHELIUM CELL; GENE THERAPY; GENE VECTOR; GENETIC TRANSDUCTION; HEART MUSCLE CELL; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS; RAT;

ADENOVIRIDAE; ANIMALS; CATTLE; ENDOTHELIAL CELLS; GENE THERAPY; GENETIC VECTORS; HIV; HUMANS; MYOCYTES, CARDIAC; RATS; TRANSDUCTION, GENETIC;

ADENOVIRIDAE; BOS TAURUS; HUMAN IMMUNODEFICIENCY VIRUS; LENTIVIRUS;

EID: 33845437506     PISSN: 10826068     EISSN: 15322297     Source Type: Journal    
DOI: 10.1080/10826060601039345     Document Type: Article

References (22)

1. Kahn, M.L.; Lee, S.W.; Dichek, D.A. Optimization of retroviral vector-mediated gene transfer into endothelial cells in vitro. Circ. Res. 1992, 71, 1508-1517.
2. Merrick, A.F.; Shewring, L.D.; Sawyer, G.T.; Gustafsson, K.T.; Fabre, J.W. Comparison of adenovirus gene transfer to vascular endothelial cells in cell cultures, organ culture, and in vivo. Transplantation 1996, 62, 1085-1089.
3. Mulligan, R.C. The basic science of gene therapy. Science 1993, 260, 926-932.
4. Tanner, F.C.; Carr, D.P.; Nabel, G.J.; Nabel, E.G. Transfection of human endothelial cells. Cardiovasc. Res. 1997, 35, 522-528.
5. Shi, Y.; Fard, A.; Vermani, P.; Zalewski, A. Transgene expression in the coronary circulation transcatheter gene delivery. Gene Ther. 1994, 1, 408-414.
6. Shulick, A.H.; Newman, K.D.; Vermani, R.; Dichek, D.A. In vivo gene transfer into injured carotid arteries. Optimization and evaluation of acute toxicity. Circulation 1995, 91, 2407-2414.
7. Lewis, P.F.; Emerman, M. Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus. J. Viol. 1994, 68, 510-516.
8. Naldini, L.; Blomer, U.; Gallay, P.; Ory, D.; Mulligan, R.; Gage, F.H.; Vrma, I.M.; Trono, D. In vivo gene delivery and stable transduction of nondividing cells by a lentivairal vector. Science 1996, 272, 263-267.
9. Burns, J.C.; Friedman, T.; Driever, W.; Burrascano, M.; Yee, J.K. Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: Concentration to very high titer and efficient gene transfer into mammalian and non mammrian cells. Proc. Natl. Acad. Sci. USA 1993, 90, 8033-8037.
10. Naldini, L.; Blomer, U.; Gage, F.H.; Trono, D.; Verma, I.M. Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains with a lentiviral vector. Proc. Natl. Acad. Sci. USA 1996, 93, 11382-11388.
11. Miyake, K.; Suzuki, N.; Matsuoka, H.; Tpyama, T.; Shimada, T. Stable integration of human immunodeficiency virus-based retroviral vectors into the chromosomes of nondividing cells. Hum. Gene Ther. 1998, 9, 467-475.
12. Hirata, K.; Miki, N.; Kuroda, Y.; Sakoda, T.; Kawashima, S.; Yokoyama, M. Low concentration of oxidized low-density lipoprotein and lysophosphatidylcholine upregulate constitutive nitric oxide synthase mRNA expression in bovine aortic endothelial cells. Circ. Res. 1995, 76, 958-962.
13. Sakoda, T.; Kasahara, N.; Hamamori, Y.; Kedes, L. A high-titer lentiviral production system mediates efficient transfuction of differentiated cells including beating cardiac myocyets. J. Mol. Cell. Cardiol. 1999, 31, 2037-2047.
14. Kurabayashi, M.; Dutta, S.; Kedes, L. Serum-inducible factors binding to an activating transcription factor motif regulate transcription of the Id2A promoter during myogenic differentiation. J. Biol. Chem. 1994, 269, 31162-31170.
15. Chen, C.; Okayama, H. High efficiency transformation of mammalian cells by plasmid DNA. Mol. Cell Biol. 1987, 7, 2745-2752.
16. Sakoda, T.; Kaibuchi, K.; Kishi, K.; Kishida, S.; Doi, K.; Hoshino, M.; Hattori, S.; Takai, Y. Smg/rap1/Krev-1 p21s inhibit the signal pathway to the c-fos promoter/enhancer from c-Ki-ras p21 but not from c-raf-1 kinase in NIH3T3 cells. Oncogene 1992, 7, 1705-1711.
17. Price, J.; Turner, D.; Cepko, C. Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. Proc. Natl. Acad. Sci. USA 1987, 84, 156-160.
18. Ueyama, T.; Kawashima, S.; Sakoda, T.; Rikitake, Y.; Ishida, T.; Kawai, M.; Yamashita, T.; Ishido, S.; Hotta, H.; Yokoyama, M. Requirement of activation of the extracellular signal-regulated kinase cascade in myocardial cell hypertrophy. J. Mol. Cell Cardiol. 2000, 32, 947-960.
19. Sanes, J.R.; Rubenstein, J.L.R.; Nicolas, J.F. Use of recombinant retrovirus tos tudy post-implantation cell lineage in mouse embryos. EMBO J. 1986, 5, 3133-3142.
20. Nabel, E.G.; Plautz, G.; Boyce, F.M.; Stanley, J.C.; Nabel, G.J. Science 1989, 244, 1342-1344.
21. Quantin, B.; Perricaudet, L.D.; Tajbakhsh, S.; Mandel, J.L. Adenovirus as an expression vector in muscle cells in vivo. Proc. Natl. Acad. Sci. USA 1990, 87, 439-443.
22. Knowlees, M.R.; Hohneker, K.W.; Zhou, Z.; Olsen, J.C.; Npah, T.L.; Hu, P.C.; Leigh, M.W.; Engelhardt, J.F.; Edwards, L.J.; Jones, K.R. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. New Engl. J. Med. 1995, 333, 823-831.