Adenovirus-mediated gene delivery and in vitro microinsemination produce offspring from infertile male mice

被引:60
作者
Kanatsu-Shinohara, M
Ogura, A
Ikegawa, M
Inoue, K
Ogonuki, N
Tashiro, K
Toyokuni, S
Honjo, T
Shinohara, T [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Med Chem, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Pathol & Biol Dis, Kyoto 6068501, Japan
[3] Kyoto Univ, Grad Sch Med, Ctr Mol Biol & Genet, Kyoto 6068507, Japan
[4] Natl Inst Infect Dis, Dept Vet Sci, Tokyo 1628640, Japan
关键词
D O I
10.1073/pnas.022646399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sertoli cells play a pivotal role in spermatogenesis through their interactions with germ cells. To set up a strategy for treating male infertility caused by Sertoli cell dysf unction, we developed a Sertoli cell gene transfer system by using an adenovirus vector, which maintained long-term transgene expression in the testes of infertile mice. Introduction of an adenovirus carrying the mouse Steel (Sl) gene into Sertoli cells restored partial spermatogenesis in infertile Steel/Steel(dickie) (Sl/Sl(d)) mutant mouse testes. Although these males remained infertile, round spermatids and spermatozoa from the testes produced normal fertile offspring after intracytoplasmic injection into oocytes. None of the offspring showed evidence of germ line transmission of adenoviral DNA. Thus, we demonstrate a successful treatment for infertility by using a gene therapy vector. Therefore, adenovirus-mediated gene delivery into Sertoli cells not only provides an efficient and convenient means for studying germ cell-Sertoli cell interactions through manipulation of the germ cell microenvironment in vivo, but also is a useful method to treat male infertility resulting from a Sertoli cell defect.
引用
收藏
页码:1383 / 1388
页数:6
相关论文
共 52 条
[1]  
BARKER CF, 1977, ADV IMMUNOL, V25, P1
[2]   A ROLE FOR CD95 LIGAND IN PREVENTING GRAFT-REJECTION [J].
BELLGRAU, D ;
GOLD, D ;
SELAWRY, H ;
MOORE, J ;
FRANZUSOFF, A ;
DUKE, RC .
NATURE, 1995, 377 (6550) :630-632
[3]  
BELLVE AR, 1993, METHOD ENZYMOL, V225, P84
[4]   Adenovirus-mediated gene transfer to rat testis in vivo [J].
Blanchard, KT ;
Boekelheide, K .
BIOLOGY OF REPRODUCTION, 1997, 56 (02) :495-500
[5]   DEVELOPMENTAL ABNORMALITIES IN STEEL(17H) MICE RESULT FROM A SPLICING DEFECT IN THE STEEL FACTOR CYTOPLASMIC TAIL [J].
BRANNAN, CI ;
BEDELL, MA ;
RESNICK, JL ;
EPPIG, JJ ;
HANDEL, MA ;
WILLIAMS, DE ;
LYMAN, SD ;
DONOVAN, PJ ;
JENKINS, NA ;
COPELAND, NG .
GENES & DEVELOPMENT, 1992, 6 (10) :1832-1842
[6]   SPERMATOGENESIS FOLLOWING MALE GERM-CELL TRANSPLANTATION [J].
BRINSTER, RL ;
ZIMMERMANN, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11298-11302
[7]   Isolation of germ cells from human testicular tissue for low temperature storage and autotransplantation [J].
Brook, PF ;
Radford, JA ;
Shalet, SM ;
Joyce, AD ;
Gosden, RG .
FERTILITY AND STERILITY, 2001, 75 (02) :269-274
[8]   EFFECTS OF BUSULFAN ON MURINE SPERMATOGENESIS - CYTOTOXICITY, STERILITY, SPERM ABNORMALITIES, AND DOMINANT LETHAL MUTATIONS [J].
BUCCI, LR ;
MEISTRICH, ML .
MUTATION RESEARCH, 1987, 176 (02) :259-268
[9]   THE PROTO-ONCOGENE C-KIT ENCODING A TRANSMEMBRANE TYROSINE KINASE RECEPTOR MAPS TO THE MOUSE W-LOCUS [J].
CHABOT, B ;
STEPHENSON, DA ;
CHAPMAN, VM ;
BESMER, P ;
BERNSTEIN, A .
NATURE, 1988, 335 (6185) :88-89
[10]  
DELCASTILLO EB, 1947, J CLIN ENDOCRINOL, V7, P493