Highly efficient gene delivery into transfection-refractory neuronal and astroglial cells using a retrovirus-based vector

被引:0
|
作者
Kim, BO [1 ]
Pyo, S
机构
[1] Sangju Natl Univ, Coll Life Sci & Nat Resources, Dept Appl Biol, Sangju 742711, South Korea
[2] Sungkyunkwan Univ, Coll Pharm, Div Immunopharmacol, Suwon 4407710, South Korea
关键词
retrovirus-mediated gene delivery; neuronal cell; astroglial cells; retrovirus-based vector;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction of foreign genes into brain cells, such as neurons and astrocytes, is a powerful approach to study the gene function and regulation in the neuroscience field. Calcium phosphate precipitates have been shown to cause cytotoxicity in some mammalian cells and brain cells, thus leading to low transfection efficiency. Here, we describe a retrovirus-mediated gene delivery method to transduce foreign genes into brain cells. In an attempt to achieve higher gene delivery efficiency in these cells, we made several changes to the original method, including (1) use of a new packaging cell line, Phoenix ampho cells, (2) transfection of pMX retroviral DNA, (3) inclusion of 25 mM chloroquine in the transduction, and (4) 3- 5 h incubation of retroviruses with target cells. The results showed that the modified protocol resulted in a range of 40- 60% gene delivery efficiency in neurons and astrocytes. Furthermore, these results suggest the potential of the retrovirus-mediated gene delivery protocol being modified and adapted for other transfection-reftactory cell lines and primary cells.
引用
收藏
页码:451 / 454
页数:4
相关论文
共 33 条
  • [1] Delivery of dominant-negative inhibitors of HIV protease to PBMC using a retrovirus-based gene therapy vector
    Todd, S
    Anderson, CG
    Jolly, DJ
    Laboissiere, MCA
    Craik, CS
    FASEB JOURNAL, 1999, 13 (07): : A1591 - A1591
  • [2] Adenovirus vector-based highly efficient recovery system of retrovirus from defective retrovirus infected cells.
    Shirane, D
    Kohtarh, S
    Hirose, K
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2003, 91 : 280P - 280P
  • [3] Highly Efficient Lentivirus-Based Vector for Gene Delivery in Immunodeficiency Purposes
    Karimi, A.
    Masoud, N.
    Pourghaysari, B.
    Shirzad, H.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 : S497 - S497
  • [4] Dual Peptide-Based Gene Delivery System for the Efficient Transfection of Plant Callus Cells
    Miyamoto, Takaaki
    Tsuchiya, Kousuke
    Numata, Keiji
    BIOMACROMOLECULES, 2020, 21 (07) : 2735 - 2744
  • [5] Non-toxic, highly efficient delivery of nucleic acids into challenging cells using safectin transfection reagent
    Howell, Steve
    Bradley, Mark
    Unciti-Broceta, Asier
    DRUG DISCOVERY TODAY, 2010, 15 (23-24) : 1114 - 1114
  • [6] Highly efficient non-viral delivery of macromolecules to unactivated human T cells using microfluidic transfection
    Chehal, Manreet
    Ouellet, Eric
    Binson, Elinor
    Nguyen, Quan
    Liao, Tina
    Chau, Phillip
    Chen, Kris
    Lambertz, Ulrike
    Yu, Jessie
    Chen, Kevin
    Loughhead, Scott
    Dalton, Bob
    Eaves, Allen
    Louis, Sharon
    Kokaji, Andy
    JOURNAL OF IMMUNOLOGY, 2024, 212 (01):
  • [7] Baculovirus as a highly efficient gene delivery vector for the expression of hepatitis delta virus antigens in mammalian cells
    Wang, KC
    Wu, JC
    Chung, YC
    Ho, YC
    Chang, MDT
    Hu, YC
    BIOTECHNOLOGY AND BIOENGINEERING, 2005, 89 (04) : 464 - 473
  • [8] Gene delivery into neuronal and glial cells by using a replication-deficient adenovirus vector: Prospects for neurological gene therapy
    Sivasubramaniam, S
    Fooks, A
    Lee, J
    Stacey, G
    Jennings, A
    CYTOTECHNOLOGY, 1997, 24 (03) : 253 - 259
  • [9] Gene delivery into neuronal and glial cells by using a replication-deficient adenovirus vector: prospects for neurological gene therapy
    ShivaDas Sivasubramaniam
    Anthony Fooks
    John Lee
    Glyn Stacey
    Alan Jennings
    Cytotechnology, 1997, 24 : 253 - 259
  • [10] Alpha-Retrovirus-Based Virus-Like Particles for Efficient Gene Editor Delivery into Hematopoietic Stem Cells
    Klatt, Denise
    Mayer, Josephine
    Zeng, Jing
    Zhang, Chi-Yuan
    Neri, Nola
    Levesque, Sebastien
    Schambach, Axel
    Verhoeyen, Els
    Bauer, Daniel E.
    Williams, David A.
    Brendel, Christian
    MOLECULAR THERAPY, 2024, 32 (04) : 107 - 108