Primate spermatogonial stem cells colonize mouse testes

被引:148
作者
Nagano, M
McCarrey, JR
Brinster, RL
机构
[1] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
[2] SW Fdn Biomed Res, Dept Genet, San Antonio, TX 78245 USA
[3] SW Reg Primate Res Ctr, San Antonio, TX 78245 USA
关键词
Sertoli cells; spermatogenesis; testis;
D O I
10.1095/biolreprod64.5.1409
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In mice, transplantation of spermatogonial stem cells from a fertile male to the seminiferous tubules of an infertile recipient male results in progeny with donor-derived haplotype. Attempts to extend this approach by transplanting human testis cells to mice have led to conflicting claims that no donor germ cells persisted or that human spermatozoa were produced in the recipient. To examine this issue we used the baboon, a primate in which testis cell populations of several ages could be obtained for transplantation, and demonstrate that donor spermatogonial stem cells readily establish germ cell colonies in recipient mice, which exist for periods of at least 6 mo. However, differentiation of germ cells toward the lumen of the tubule and production of spermatozoa did not occur. The presence of baboon spermatogonial stem cells and undifferentiated spermatogonia in mouse seminiferous tubules for long periods after transplantation indicates that antigens, growth factors, and signaling molecules that are necessary for interaction of these cells and the testis environment have been preserved for 100 million years of evolutionary separation. Because germ cell differentiation and spermatogenesis did not occur, the molecules necessary for this process appear to have undergone greater divergence between baboon and mouse.
引用
收藏
页码:1409 / 1416
页数:8
相关论文
共 49 条
[41]  
Russell LD, 1990, HISTOLOGICAL HISTOPA, P62
[42]   Functional analysis of spermatogonial stem cells in Steel and cryptorchid infertile mouse models [J].
Shinohara, T ;
Avarbock, MR ;
Brinster, RL .
DEVELOPMENTAL BIOLOGY, 2000, 220 (02) :401-411
[43]   β1- and α6-integrin are surface markers on mouse spermatogonial stem cells [J].
Shinohara, T ;
Avarbock, MR ;
Brinster, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5504-5509
[44]   Spermatogonial stem cell enrichment by multiparameter selection of mouse testis cells [J].
Shinohara, T ;
Orwig, KE ;
Avarbock, MR ;
Brinster, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8346-8351
[45]  
SOFIKITIS N, 1999, FERTIL STERIL S1, V72, P83
[46]  
TEGELENBOSCH RAJ, 1993, MUTAT RES, V290, P193
[47]   REPOPULATION OF THE SEMINIFEROUS EPITHELIUM OF THE RHESUS-MONKEY AFTER X-IRRADIATION [J].
VANALPHEN, MMA ;
VANDEKANT, HJG ;
DEROOIJ, DG .
RADIATION RESEARCH, 1988, 113 (03) :487-500
[48]   SYNCHRONIZATION OF THE SEMINIFEROUS EPITHELIUM AFTER VITAMIN-A REPLACEMENT IN VITAMIN A-DEFICIENT MICE [J].
VANPELT, AMM ;
DEROOIJ, DG .
BIOLOGY OF REPRODUCTION, 1990, 43 (03) :363-367
[49]   Out of Eden: Stem cells and their niches [J].
Watt, FM ;
Hogan, BLM .
SCIENCE, 2000, 287 (5457) :1427-1430