Clinical aspects of male germ cell apoptosis during testis development and spermatogenesis

被引:94
作者
Dunkel, L
Hirvonen, V
Erkkila, K
机构
[1] Children's Hospital, University of Helsinki
关键词
androgens; apoptosis; cryptorchidism; germ cell; hCG; prepuberty; programmed cell death; spermatogenesis; testosterone;
D O I
10.1038/sj.cdd.4400234
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis appears to have an essential role in the control of germ cell number in testes. During spermatogenesis germ cell deletion has been estimated to result in the loss of up to 75% of the potential number of mature sperm cells. At least three factors seem to determine the onset of apoptosis in male germ cells: (1) lack of hormones, especially gonadotropins and androgens; (2) the specific stage in the spermatogenic cycle; (3) and the developmental stage of the animal. Although male germ cell apoptosis has been well characterized in various animal models, few studies are presently available regarding germ cell apoptosis in the human testis. The first part of this review is focused on germ cell apoptosis in testes of prepubertal boys, with special emphasis on apoptosis in normal and cryptorchid testes. A higher percentage of apoptotic spermatogonia was seen in the cryptorchid testes than in the scrotal testes. The hCG-treatment increased the number of apoptotic spermatogonia. The hCG-treatment-induced apoptosis in spermatogonia had severe long-term consequences in reproductive functions in adulthood. Increased apoptosis after hCG-treatment was associated with subnormal testis volumes, subnormal sperm density and pathologically elevated serum FSH. This finding indicates that increased apoptosis in spermatogonia in prepuberty leads to disruption of testis development. To evaluate the role of apoptosis in human adult testes, apoptosis was induced in seminiferous tubules that were incubated under serum-free conditions in the absence or presence of testosterone. Most frequently apoptosis was identified in spermatocytes. Occasionally some spermatids also showed signs of apoptosis. In short term incubations apoptosis was suppressed by testosterone. Our findings lead to the conclusion that apoptosis is a normal, hormonally controlled phenomenon in the human testis. The role of apoptosis in disorders of spermatogenesis remains to be established.
引用
收藏
页码:171 / 179
页数:9
相关论文
共 55 条
[1]   EXPRESSION OF CLUSTERIN IN CELL-DIFFERENTIATION AND CELL-DEATH [J].
AHUJA, HS ;
TENNISWOOD, M ;
LOCKSHIN, R ;
ZAKERI, ZF .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1994, 72 (11-12) :523-530
[2]   SPERMATOGONIAL APOPTOSIS HAS 3 MORPHOLOGICALLY RECOGNIZABLE PHASES AND SHOWS NO CIRCADIAN-RHYTHM DURING NORMAL SPERMATOGENESIS IN THE RAT [J].
ALLAN, DJ ;
HARMON, BV ;
ROBERTS, SA .
CELL PROLIFERATION, 1992, 25 (03) :241-250
[3]   FSH AND TESTOSTERONE, ALONE OR IN COMBINATION, INITIATE TESTICULAR GROWTH AND INCREASE THE NUMBER OF SPERMATOGONIA AND SERTOLI CELLS IN A JUVENILE NONHUMAN PRIMATE (MACACA-MULATTA) [J].
ARSLAN, M ;
WEINBAUER, GF ;
SCHLATT, S ;
SHAHAB, M ;
NIESCHLAG, E .
JOURNAL OF ENDOCRINOLOGY, 1993, 136 (02) :235-+
[4]   A ROLE FOR CD95 LIGAND IN PREVENTING GRAFT-REJECTION [J].
BELLGRAU, D ;
GOLD, D ;
SELAWRY, H ;
MOORE, J ;
FRANZUSOFF, A ;
DUKE, RC .
NATURE, 1995, 377 (6550) :630-632
[5]   APOPTOSIS IN TESTIS GERM-CELLS - DEVELOPMENTAL-CHANGES IN GONADOTROPIN DEPENDENCE AND LOCALIZATION TO SELECTIVE TUBULE STAGES [J].
BILLIG, H ;
FURUTA, I ;
RIVIER, C ;
TAPANAINEN, J ;
PARVINEN, M ;
HSUEH, AJW .
ENDOCRINOLOGY, 1995, 136 (01) :5-12
[6]   SPERMATOGONIAL CELL-PROLIFERATION IN ORGAN-CULTURE OF IMMATURE RAT TESTIS [J].
BOITANI, C ;
POLITI, MG ;
MENNA, T .
BIOLOGY OF REPRODUCTION, 1993, 48 (04) :761-767
[7]   INDUCTION OF THE TRPM-2 GENE IN CELLS UNDERGOING PROGRAMMED DEATH [J].
BUTTYAN, R ;
OLSSON, CA ;
PINTAR, J ;
CHANG, CS ;
BANDYK, M ;
NG, PY ;
SAWCZUK, IS .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (08) :3473-3481
[8]  
CHILVERS CED, 1992, ARCH DIS CHILD, V67, P892
[9]   QUANTITATIVE ANALYSIS OF SPERMATOGENESIS OF RAT - A REVISED MODEL FOR RENEWAL OF SPERMATOGONIA [J].
CLERMONT, Y .
AMERICAN JOURNAL OF ANATOMY, 1962, 111 (02) :111-&
[10]   RENEWAL OF SPERMATOGONIA IN MAN [J].
CLERMONT, Y .
AMERICAN JOURNAL OF ANATOMY, 1966, 118 (02) :509-&