Cellular distribution of transforming growth factor betas 1, 2, and 3 and their types I and II receptors during postnatal development and spermatogenesis in the boar testis

被引:48
作者
Caussanel, V
Tabone, E
Hendrick, JC
Dacheux, F
Benahmed, M
机构
[1] CTR HOSP LYON SUD, INSERM U407, BIOCHIM LAB, F-69495 PIERRE BENITE, FRANCE
[2] CTR LEON BERARD, UNITE PATHOL ULTRASTRUCT, F-69373 LYON, FRANCE
[3] PRMD, URA, INRA, CNRS 1291, NOUZILLY, FRANCE
[4] UNIV LIEGE, LAB RADIOIMMUNOL, LIEGE, BELGIUM
关键词
D O I
10.1095/biolreprod56.2.357
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transforming growth factor betas (TCF beta s) 1, 2, and 3 and their types I and II receptors (TCF beta s RI and RII) were immunolocalized 1) during testicular development from the perinatal to the adult period and 2) in maturing germ cell populations at successive seminiferous epithelium stages. In the perinatal testis, TGF beta isoforms and receptors were both preponderant in Leydig cells and in spermatogonia. At prepuberty, their expression appeared in Sertoli cells, while germ cells showed specific TGF beta 1 and TGF beta RI staining in the spermatocytes. In the adult testis, TGF beta ligands exhibited a preferential tubular distribution. TGF beta 1 was mainly detected in young spermatocytes, TGF beta 2 in Sertoli cells, and TGF beta 3 in Sertoli and premeiotic germ cells. Although the two receptors were systematically observed together in various cells, our data indicate a predominance of one in comparison with the other depending on the cell type. TGF beta RI was predominant in meiotic and differentiated germ cells and TGF beta RII in somatic cells. Finally, in the adult testis, TCF beta s 1, 3, and RI showed a germ-cell pattern that depended upon the stage of the seminiferous epithelium cycle. Specifically, staining for the ligands was predominant before meiosis, and TGF beta RI was present particularly during meiosis and spermiogenesis. Together, the temporal and spatial distribution of the TGF beta system components suggests that these signaling molecules may play a crucial role during specific steps of testicular development and during different waves of seminiferous epithelium maturation leading to spermatogenesis.
引用
收藏
页码:357 / 367
页数:11
相关论文
共 52 条
[11]  
De Kretser D. M., 1994, P1177
[12]   COMPLEMENTARY-DNA FOR HUMAN GLIOBLASTOMA-DERIVED T-CELL SUPPRESSOR FACTOR, A NOVEL MEMBER OF THE TRANSFORMING GROWTH FACTO-BETA GENE FAMILY [J].
DEMARTIN, R ;
HAENDLER, B ;
HOFERWARBINEK, R ;
GAUGITSCH, H ;
WRANN, M ;
SCHLUSENER, H ;
SEIFERT, JM ;
BODMER, S ;
FONTANA, A ;
HOFER, E .
EMBO JOURNAL, 1987, 6 (12) :3673-3677
[13]   A NEW TYPE OF TRANSFORMING GROWTH FACTOR-BETA, TGF-BETA-3 [J].
DERYNCK, R ;
LINDQUIST, PB ;
LEE, A ;
WEN, D ;
TAMM, J ;
GRAYCAR, JL ;
RHEE, L ;
MASON, AJ ;
MILLER, DA ;
COFFEY, RJ ;
MOSES, HL ;
CHEN, EY .
EMBO JOURNAL, 1988, 7 (12) :3737-3743
[14]   SEQUENCE OF THE PORCINE TRANSFORMING GROWTH-FACTOR-BETA PRECURSOR [J].
DERYNCK, R ;
RHEE, L .
NUCLEIC ACIDS RESEARCH, 1987, 15 (07) :3187-3187
[16]   DIRECT REGULATING EFFECTS OF TRANSFORMING GROWTH FACTOR-BETA-1 ON LACTATE PRODUCTION IN CULTURED PORCINE SERTOLI CELLS [J].
ESPOSITO, G ;
KERAMIDAS, M ;
MAUDUIT, C ;
FEIGE, JJ ;
MORERA, AM ;
BENAHMED, M .
ENDOCRINOLOGY, 1991, 128 (03) :1441-1449
[17]   TRANSFORMING GROWTH FACTOR-BETA STIMULATES MEIOTIC MATURATION OF THE RAT OOCYTE [J].
FENG, P ;
CATT, KJ ;
KNECHT, M .
ENDOCRINOLOGY, 1988, 122 (01) :181-186
[18]  
FRITZ IB, 1993, SERTOLI CELL, P201
[19]   IMMUNOHISTOCHEMICAL LOCALIZATION OF TRANSFORMING GROWTH FACTOR-BETA(1) IN THE FETAL AND NEONATAL RAT TESTIS [J].
GAUTIER, C ;
LEVACHER, C ;
AVALLET, O ;
VIGIER, M ;
ROUILLERFABRE, T ;
LECERF, L ;
SAEZ, J ;
HABERT, R .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 99 (01) :55-61
[20]   Transforming growth factor beta receptor expression in cultured porcine granulosa cells [J].
Goddard, I ;
Hendrick, JC ;
Benahmed, M ;
Morera, AM .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1995, 115 (02) :207-213