Functional analysis of spermatogonial stem cells in Steel and cryptorchid infertile mouse models

被引:156
作者
Shinohara, T [1 ]
Avarbock, MR [1 ]
Brinster, RL [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
关键词
spermatogonial stem cells; Steel; cryptorchid; primordial germ cells (PGCs);
D O I
10.1006/dbio.2000.9655
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Spermatogenesis is a complex and productive process that originates from stem cell spermatogonia and ultimately results in formation of mature spermatozoa. The stem cell undergoes self-renewal throughout life, but study of its biological characteristics has been difficult because a very small number (2 to 3 in 10(4) cells) exist in the testis and they can only be identified by function. Although the development of the spermatogonial transplantation technique has provided an assay system for stem cells, efficient methods to enrich stem cells have not been available. Here, we examined two infertile mouse models, Steel/Steel(Dickle)(S1/S1(d)) and experimental cryptorchid, as a source of testis cell populations enriched in stem cells. The S1/S1(d) testis showed little enrichment, which raises questions about how adult stem cell number is determined and about the currently accepted belief that adult stem cells are independent of S1 factor. The cells recovered from cryptorchid testes were enriched for stem cells 25-fold (colonies) or 50-fold (area) compared to wild-type testes. The cryptorchid condition does not affect stem cell activity, but eliminates almost all differentiated cells, and about 1 in 200 cells is a stem cell. Thus, cryptorchid testes provide an important approach for purification and characterization of spermatogonial stem cells. (C) 2000 Academic Press.
引用
收藏
页码:401 / 411
页数:11
相关论文
共 43 条
[1]  
[Anonymous], 1979, COAT COLORS MICE MOD
[2]  
BENNETT DOROTHEA, 1956, J MORPH, V98, P199, DOI 10.1002/jmor.1050980202
[3]   HEMATOPOIETIC STEM-CELLS WITH HIGH PROLIFERATIVE POTENTIAL - ASSAY OF THEIR CONCENTRATION IN MARROW BY THE FREQUENCY AND DURATION OF CURE OF W/WV MICE [J].
BOGGS, DR ;
BOGGS, SS ;
SAXE, DF ;
GRESS, LA ;
CANFIELD, DR .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (02) :242-253
[4]   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
[5]   GERMLINE TRANSMISSION OF DONOR HAPLOTYPE FOLLOWING SPERMATOGONIAL TRANSPLANTATION [J].
BRINSTER, RL ;
AVARBOCK, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11303-11307
[7]  
De Kretser D. M., 1994, P1177
[8]   Arrest of spermatogonial differentiation in js']jsd/js']jsd, Sl17H/Sl17H, and cryptorchid mice [J].
de Rooij, DG ;
Okabe, M ;
Nishimune, Y .
BIOLOGY OF REPRODUCTION, 1999, 61 (03) :842-847
[9]   Spermatogonial stem cells [J].
de Rooij, DG ;
Grootegoed, JA .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (06) :694-701
[10]  
Dobrinski I, 1999, MOL REPROD DEV, V53, P142, DOI 10.1002/(SICI)1098-2795(199906)53:2&lt