Function of stem cell factor as a survival factor of spermatogonia and localization of messenger ribonucleic acid in the rat seminiferous epithelium

被引:71
作者
Hakovirta, H
Yan, W
Kaleva, M
Zhang, FP
Vänttinen, K
Morris, PL
Söder, M
Parvinen, M
Toppari, J
机构
[1] Univ Turku, Dept Physiol, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Anat, FIN-20520 Turku, Finland
[3] Univ Turku, Dept Pediat, FIN-20520 Turku, Finland
[4] Populat Council, New York, NY 10021 USA
[5] Karolinska Inst, Pediat Endocrinol Unit, Stockholm, Sweden
关键词
D O I
10.1210/en.140.3.1492
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To address the possibility that stem cell factor (SCF) is a paracrine regulator of germ cell development in the adult rat testis, stage-specific distribution of SCF messenger RNA (mRNA) was investigated with Northern blot and in situ hybridization analyses. The highest levels of SCF mRNA were found in stages II-VI of the rat seminiferous epithelial cycle, whereas the lowest levels were in stages VII-VIII. Intermediate levels of SCF mRNA were detected in stages IX-XIV-I of the cycle. The expression of the SCF gene was found to be developmentally regulated, and the expression pattern followed the process of Sertoli cell proliferation and differentiation during postnatal life. The effect of mouse recombinant SCF on spermatogonial DNA synthesis was studied using an in vitro tissue culture system for stage-defined seminiferous tubules. A significant increase in DNA synthesis in spermatogonia could be detected when tubule segments from stage XII were cultured in the presence of 100 ng/ml SCF for 48 h (P < 0.05) and 72 h (P < 0.01). This observation was further confirmed with autoradiographic analyses; almost a 100-fold increase in thymidine incorporation in the SCF-treated (100 ng/ml) tubule segments was observed compared with that in untreated samples. The results of the present study suggest that SCF is a Sertoli cell-produced paracrine regulator and acts as a survival factor for spermatogonia in the adult rat seminiferous epithelium in a stage-specific manner.
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页码:1492 / 1498
页数:7
相关论文
共 34 条
[1]  
ANDERSON DM, 1991, CELL GROWTH DIFFER, V2, P373
[2]   The kit ligand encoded at the murine Steel locus: a pleiotropic growth and differentiation factor [J].
Besmer, Peter .
CURRENT OPINION IN CELL BIOLOGY, 1991, 3 (06) :939-946
[3]   Leuprolide, a gonadotropin-releasing hormone agonist, reestablishes spermatogenesis after 2,5-hexanedione-induced irreversible testicular injury in the rat, resulting in normalized stem cell factor expression [J].
Blanchard, KT ;
Lee, JW ;
Boekelheide, K .
ENDOCRINOLOGY, 1998, 139 (01) :236-244
[4]   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
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   MAST-CELL GROWTH-FACTOR MAPS NEAR THE STEEL LOCUS ON MOUSE CHROMOSOME-10 AND IS DELETED IN A NUMBER OF STEEL ALLELES [J].
COPELAND, NG ;
GILBERT, DJ ;
CHO, BC ;
DONOVAN, PJ ;
JENKINS, NA ;
COSMAN, D ;
ANDERSON, D ;
LYMAN, SD ;
WILLIAMS, DE .
CELL, 1990, 63 (01) :175-183
[7]   EXPRESSION OF C-KIT RECEPTOR AND ITS AUTOPHOSPHORYLATION IN IMMATURE RAT TYPE-A SPERMATOGONIA [J].
DYM, M ;
JIA, MC ;
DIRAMI, G ;
PRICE, JM ;
RABIN, SJ ;
MOCCHETTI, I ;
RAVINDRANATH, N .
BIOLOGY OF REPRODUCTION, 1995, 52 (01) :8-19
[8]   TRANSMEMBRANE FORM OF THE KIT LIGAND GROWTH-FACTOR IS DETERMINED BY ALTERNATIVE SPLICING AND IS MISSING IN THE SI(D) MUTANT [J].
FLANAGAN, JG ;
CHAN, DC ;
LEDER, P .
CELL, 1991, 64 (05) :1025-1035
[9]   THE KIT LIGAND - A CELL-SURFACE MOLECULE ALTERED IN STEEL MUTANT FIBROBLASTS [J].
FLANAGAN, JG ;
LEDER, P .
CELL, 1990, 63 (01) :185-194
[10]   THE DOMINANT-WHITE SPOTTING (W) LOCUS OF THE MOUSE ENCODES THE C-KIT PROTO-ONCOGENE [J].
GEISSLER, EN ;
RYAN, MA ;
HOUSMAN, DE .
CELL, 1988, 55 (01) :185-192