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Use of Simian Immunodeficiency Virus Vectors for Simian Embryonic Stem Cells

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Embryonic Stem Cell Protocols

Part of the book series: Methods in Molecular Biology ((MIMB,volume 329))

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Abstract

The ability to stably introduce genetic material into primate embryonic stem (ES) cells could allow broader application. In this chapter, we describe a method of gene transfer into simian (cynomolgus macaque) ES cells using a simian immunodeficiency virus-based lentivirus vector. When cynomolgus ES cells are transduced with a simian immunodeficiency virus vector encoding the green fluorescent protein (GFP) gene, a large fraction of cells (greater than 50%) fluoresce, and high levels of GFP expression persist for months as assessed by flow cytometry and real-time polymerase chain reaction. Thus, the use of GFP as a reporter gene allows direct and simple detection of successfully transduced ES cells and facilitates monitoring of ES cell proliferation and differentiation both in vitro and in vivo. In addition, this highly efficient gene transfer method allows faithful gene delivery to primate ES cells with potential for both research and therapeutic applications.

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References

  1. Thomson J. A., Kalishman J., Golos T. G., et al. (1995) Isolation of primate embryonic stem cell line. Proc. Natl. Acad. Sci. USA 92, 7844–7848.

    Article  CAS  PubMed  Google Scholar 

  2. Suemori H., Tada T., Torii R., et al. (2001) Establishment of embryonic stem cell lines from cynomolgus monkey blastocysts produced by IVF or ICSI. Dev. Dyn. 222, 273–279.

    Article  CAS  PubMed  Google Scholar 

  3. Naldini L., Blomer U., Gallay P., et al. (1996) In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272, 263–267.

    Article  CAS  PubMed  Google Scholar 

  4. Miyoshi H., Smith K. A., Mosier D. E., Verma I. M., and Torbett B. E. (1999) Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors. Science 283, 682–686.

    Article  CAS  PubMed  Google Scholar 

  5. Poeschla E. M., Wong-Staal F., and Looney D. J. (1998) Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat. Med. 4, 354–357.

    Article  CAS  PubMed  Google Scholar 

  6. Olsen J. C. (1998) Gene transfer vectors derived from equine infectious anemia virus. Gene Ther. 5, 1481–1487.

    Article  CAS  PubMed  Google Scholar 

  7. Nakajima T., Nakamaru K., Ido E., Terao K., Hayami M., and Hasegawa M. (2000) Development of novel simian immunodeficiency virus vectors carrying a dual gene expression system. Hum. Gene Ther. 11, 1863–1874.

    Article  CAS  PubMed  Google Scholar 

  8. Schnell T., Foley P., Wirth M., Munch J., and Uberla K. (2000) Development of a selfinactivating, minimal lentivirus vector based on simian immunodeficiency virus. Hum. Gene Ther. 11, 439–447.

    Article  CAS  PubMed  Google Scholar 

  9. Berkowitz R., Ilves H., Lin W. Y., et al. (2001) Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virus. J. Virol. 75, 3371–3382.

    Article  CAS  PubMed  Google Scholar 

  10. Hanazono Y., Asano T., Ueda Y., and Ozawa K. (2003) Genetic manipulation of primate embryonic and hematopoietic stem cells with simian lentivirus vectors. Trends Cardiovasc. Med. 13, 106–110.

    Article  CAS  PubMed  Google Scholar 

  11. Owens C. M., Yang P. C., Gottlinger H., and Sodroski J. (2003) Human and simian immunodeficiency virus capsid proteins are major viral determinants of early, postentry replication blocks in simian cells. J. Virol. 77, 726–731.

    Article  CAS  PubMed  Google Scholar 

  12. Stremlau M., Owens C. M., Perron M. J., Kiessling M., Autissier P., and Sodroski J. (2004) The cytoplasmic body component TRIM5alpha restricts HIV-1 infection in Old World monkeys. Nature 427, 848–853.

    Article  CAS  PubMed  Google Scholar 

  13. Asano T., Hanazono Y., Ueda Y., et al. (2002) Highly efficient gene transfer into primate embryonic stem cells with a simian lentivirus vector. Mol. Ther. 6, 162–168.

    Article  CAS  PubMed  Google Scholar 

  14. Hanawa H., Hematti P., Keyvanfar K., et al. (2004) Efficient gene transfer into rhesus repopulating hematopoietic stem cells using a simian immunodeficiency virus-based lentiviral vector system. Blood 103, 4062–4069.

    Article  CAS  PubMed  Google Scholar 

  15. Ikeda Y., Goto Y., Yonemitsu Y., et al. (2003) Simian immunodeficiency virus-based lentivirus vector for retinal gene transfer: a preclinical safety study in adult rats. Gene Ther. 10, 1161–1169.

    Article  CAS  PubMed  Google Scholar 

  16. Ogata K., Mimuro J., Kikuchi J., et al. (2004) Expression of human coagulation factor VIII in adipocytes transduced with the simian immunodeficiency virus agmTYO1-based vector for hemophilia A gene therapy. Gene Ther. 11, 253–259.

    Article  CAS  PubMed  Google Scholar 

  17. VandenDriessche T., Thorrez L., Naldini L., et al. (2002) Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo. Blood 100, 813–822.

    Article  CAS  PubMed  Google Scholar 

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© 2006 Humana Press Inc.

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Asano, T., Shibata, H., Hanazono, Y. (2006). Use of Simian Immunodeficiency Virus Vectors for Simian Embryonic Stem Cells. In: Turksen, K. (eds) Embryonic Stem Cell Protocols. Methods in Molecular Biology, vol 329. Humana Press. https://doi.org/10.1385/1-59745-037-5:295

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  • DOI: https://doi.org/10.1385/1-59745-037-5:295

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-498-2

  • Online ISBN: 978-1-59745-037-9

  • eBook Packages: Springer Protocols

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