Cochlear gene delivery through an intact round window membrane in mouse

被引:102
作者
Jero, J
Mhatre, AN
Tseng, CJ
Stern, RE
Coling, DE
Goldstein, JA
Hong, K
Zheng, WW
Hoque, ATMS
Lalwani, AK
机构
[1] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, Lab Mol Otol, Epstein Labs, San Francisco, CA 94143 USA
[2] Univ Helsinki, Cent Hosp, Dept Otolaryngol, FIN-00290 Helsinki, Finland
[3] Calif Pacific Med Ctr, Res Inst, Liposome Res Lab, San Francisco, CA 94115 USA
[4] Natl Inst Dent & Cranofacial Res, Gene Therapy & Therapeut Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1089/104303401300042465
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
Cochlear gene transfer studies in animal models have utilized mainly two delivery methods: direct injection through the round window membrane (RWM) or intracochlear infusion through a cochleostomy. However, the surgical trauma, inflammation, and hearing loss associated with these methods Lead us to investigate a less invasive delivery method. Herein, we studied the feasibility of a vector transgene-soaked gelatin sponge, Gelfoam, for transgene delivery into the mouse cochlea through an intact RWM, The Gelfoam absorbed with liposomes and adenovirus, but not with adeno-associated virus (AAV), was successful in mediating transgene expression across an intact RWM in a variety of cochlear tissues. The Gelfoam technique proved to be an easy, atraumatic, and effective, but vector-dependent, method of delivering transgenes through an intact RWM, Compared with the more invasive gene delivery methods, this technique represents a safer and a more clinically viable route of cochlear gene delivery in humans.
引用
收藏
页码:539 / 548
页数:10
相关论文
共 41 条
  • [11] Goycoolea MV, 1997, MICROSC RES TECHNIQ, V36, P201, DOI 10.1002/(SICI)1097-0029(19970201)36:3<201::AID-JEMT8>3.3.CO
  • [12] 2-F
  • [13] GOYCOOLEA MV, 1988, LARYNGOSCOPE S, V44, P1
  • [14] Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector
    Han, JJ
    Mhatre, AN
    Wareing, M
    Pettis, R
    Gao, WQ
    Zufferey, RN
    Trono, D
    Lalwani, AK
    [J]. HUMAN GENE THERAPY, 1999, 10 (11) : 1867 - 1873
  • [15] Stabilization of cationic liposome-plasmid DNA complexes by polyamines and poly(ethylene glycol)-phospholipid conjugates for efficient in vivo gene delivery
    Hong, KL
    Zheng, WW
    Baker, A
    Papahadjopoulos, D
    [J]. FEBS LETTERS, 1997, 400 (02) : 233 - 237
  • [16] Construction and function of a recombinant adenovirus encoding a human aquaporin 1-green fluorescent protein fusion product
    Hoque, ATMS
    Liu, XB
    Kagami, H
    Swaim, WD
    Wellner, RB
    O'Connell, BC
    Ambudkar, IS
    Baum, BJ
    [J]. CANCER GENE THERAPY, 2000, 7 (03) : 476 - 485
  • [17] A surgical approach appropriate for targeted cochlear gene therapy in the mouse
    Jero, J
    Tseng, CJ
    Mhatre, AN
    Lalwani, AK
    [J]. HEARING RESEARCH, 2001, 151 (1-2) : 106 - 114
  • [18] Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus
    Lalwani, AK
    Walsh, BJ
    Reilly, PG
    Carvalho, GJ
    Zolotukhin, S
    Muzyczka, N
    Mhatre, AN
    [J]. GENE THERAPY, 1998, 5 (02) : 277 - 281
  • [19] Lalwani AK, 1998, AM J OTOL, V19, P390
  • [20] Lalwani AK, 1996, GENE THER, V3, P588