RELATIONSHIP OF A MOUSE SERTOLI-CELL LINE (MSC-1) TO NORMAL SERTOLI CELLS

被引:74
作者
MCGUINNESS, MP
LINDER, CC
MORALES, CR
HECKERT, LL
PIKUS, J
GRISWOLD, MD
机构
[1] WASHINGTON STATE UNIV, DEPT BIOCHEM & BIOPHYS, PULLMAN, WA 99164 USA
[2] MCGILL UNIV, DEPT ANAT, MONTREAL H3A 2B2, PQ, CANADA
关键词
D O I
10.1095/biolreprod51.1.116
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recently, a mouse Sertoli cell line (MSC-1) was established from transgenic mice carrying a fusion gene composed of human Mullerian inhibitory substance transcriptional regulatory sequences linked to the SV40 T-antigen gene. This cell line contained a morphologically heterogeneous population of cells that expressed characteristic Sertoli cell mRNAs such as transferrin, the beta-subunit for inhibin, and sulfated glycoprotein-2 (SGP-2). In this study, we compared various characteristics of MSC-1 cells to primary cultures of Sertoli cells from immature rats or adult mice. Our observations indicated that: 1) These cells were ultrastructurally similar to mouse Sertoli cells in culture; 2) MSC-1 cells expressed mRNA for androgen-binding protein (ABP) and SGP-1, but not the receptor for FSH; 3) The expression of SGP-2 mRNA and secretion of SGP-2 increased approximately 2-fold when cells were cultured at 41 degrees C, the nonpermissive temperature for the SV40 virus, while SGP-1 and transferrin mRNA levels and secretion were unaffected; 4) Proliferation of these cells was serum-dose dependent and temperature dependent and could be inhibited by incubating MSC-1 cells at 41 degrees C; 5) Proliferation was also significantly reduced after cells were incubated in the presence of dibutyryl cAMP (dbcAMP) for 6 days; 6) Fifteen subcultures produced from single MSC-1 cells displayed similar levels of mRNA expression for transferrin or SGP-1. Together these data indicate that the MSC-1 cell line is composed of a single cell type displaying numerous characteristics of Sertoli cells. This cell line may provide a unique source of tissue for studying various aspects of Sertoli cell behavior.
引用
收藏
页码:116 / 124
页数:9
相关论文
共 43 条
[1]  
BYERS SW, 1986, J ANDROL, V7, P59
[2]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[3]   RAT TESTICULAR TESTIBUMIN IS A PROTEIN RESPONSIVE TO FOLLICLE-STIMULATING-HORMONE AND TESTOSTERONE THAT SHARES IMMUNODETERMINANTS WITH ALBUMIN [J].
CHENG, CY ;
BARDIN, CW .
BIOCHEMISTRY, 1986, 25 (18) :5276-5288
[4]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[5]  
DJAKLEW D, 1992, SERTOLI CELL, P181
[6]   CELLULAR LOCALIZATION OF 5-ALPHA-REDUCTASE AND 3-ALPHA-HYDROXYSTEROID DEHYDROGENASE IN SEMINIFEROUS TUBULE OF RAT TESTIS [J].
DORRINGTON, JH ;
FRITZ, IB .
ENDOCRINOLOGY, 1975, 96 (04) :879-889
[7]   EFFECTS OF FOLLICLE-STIMULATING HORMONE ON CULTURES OF SERTOLI CELL PREPARATIONS [J].
DORRINGTON, JH ;
ROLLER, NF ;
FRITZ, IB .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1975, 3 (01) :57-70
[8]   AN ELEMENTARY INTRODUCTION TO STEREOLOGY (QUANTITATIVE MICROSCOPY) [J].
ELIAS, H ;
HYDE, DM .
AMERICAN JOURNAL OF ANATOMY, 1980, 159 (04) :411-446
[9]   STEREOLOGY - APPLICATIONS TO BIOMEDICAL RESEARCH [J].
ELIAS, H ;
HENNIG, A ;
SCHWARTZ, DE .
PHYSIOLOGICAL REVIEWS, 1971, 51 (01) :158-&
[10]  
ELINGTON JSH, 1977, MOL CELL ENDOCRINOL, V6, P203