Testicular expression of survivin and human telomerase reverse transcriptase (hTERT) associated with spermatogenic function in infertile patients

被引:15
作者
Weikert, S
Christoph, F
Schulze, W
Krause, H
Kempkensteffen, C
Schostak, M
Miller, K
Schrader, M
机构
[1] Charite Univ Med Berlin, Dept Urol, D-12200 Berlin, Germany
[2] Univ Hamburg, Dept Androl, D-20246 Hamburg, Germany
关键词
survivin; human telomerase reverse transcriptase; apoptosis; azoospermia; male infertility; spermatogenesis;
D O I
10.1111/j.1745-7262.2006.00102.x
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Aim: To characterize the coexpression of survivin, an inhibitor of apoptosis (IAF), and human telomerase reverse transcriptase (hTERT) in human testes with varying spermatogenic function. Methods: Transcript levels of survivin mRNA and hTERT mRNA were determined in normal testes (n = 11) and testes with defective spermatogenesis (n = 28) using real-time reverse-transcription polymerase chain reaction (RT-PCR). The histological work-up was performed according to a modified Johnsen score. Results: Expressions of both survivin and hTERT were highest at median levels of 96.8 and 709 in normal spermatogenesis and dropped to 53.3 and 534 in testes with postmeiotic spermatogenic arrest (n = 10). In severe spermatogenic failure (n = 18), survivin expression was lacking in most specimens (n = 16), whereas at least low levels of testicular hTERT expression were largely detectable with a normalized expression of 73 in premeiofic spermatogenic arrest (n = 7) and 45 in patients with Sertoli cell-only syndrome (SCOS) (n = 3). Both survivin and hTERT expressions increased with a progressing Johnsen score (P for trend = 0.001). Conclusion: Although both survivin and hTERT are correlated with spermatogenic function, they show different expression patterns in testes of infertile patients. These findings substantiate results from studies in the rodent testis suggesting a predominant expression of survivin in meiotically dividing germ cells.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 22 条
[1]   Telomerase activity in female and male rat germ cells undergoing meiosis and in early embryos [J].
Eisenhauer, KM ;
Gerstein, RM ;
Chiu, CP ;
Conti, M ;
Hsueh, AJW .
BIOLOGY OF REPRODUCTION, 1997, 56 (05) :1120-1125
[2]   Survivin enhances telomerase activity via up-regulation of specificity protein 1-and c-Myc-mediated human telomerase reverse transcriptase gene transcription [J].
Endoh, T ;
Tsuji, N ;
Asanuma, K ;
Yagihashi, A ;
Watanabe, N .
EXPERIMENTAL CELL RESEARCH, 2005, 305 (02) :300-311
[3]   Telomerase activity in the testis of infertile patients with selected causes [J].
Fujisawa, M ;
Tanaka, H ;
Tatsumi, N ;
Okada, H ;
Arakawa, S ;
Kamidono, S .
HUMAN REPRODUCTION, 1998, 13 (06) :1476-1479
[4]   Telomere dysfunction triggers developmentally regulated germ cell apoptosis [J].
Hemann, MT ;
Rudolph, KL ;
Strong, MA ;
DePinho, RA ;
Chin, L ;
Greider, CW .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (07) :2023-2030
[5]   Understanding spermatogenesis is a prerequisite for treatment [J].
Adolf-Friedrich Holstein ;
Wolfgang Schulze ;
Michail Davidoff .
Reproductive Biology and Endocrinology, 1 (1)
[6]   Expression of a murine homologue of the inhibitor of apoptosis protein is related to cell proliferation [J].
Kobayashi, K ;
Hatano, M ;
Otaki, M ;
Ogasawara, T ;
Tokuhisa, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1457-1462
[7]  
Kyo S, 1999, CANCER RES, V59, P5917
[8]   In situ end-labeling of human testicular tissue demonstrates increased apoptosis in conditions of abnormal spermatogenesis [J].
Lin, WW ;
Lamb, DJ ;
Wheeler, TM ;
Lipshultz, LI ;
Kim, ED .
FERTILITY AND STERILITY, 1997, 68 (06) :1065-1069
[9]   Irregular telomeres impair meiotic synapsis and recombination in mice [J].
Liu, L ;
Franco, S ;
Spyropoulos, B ;
Moens, PB ;
Blasco, MA ;
Keefe, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6496-6501
[10]  
ORGANISATION W.H., 1999, WHO LAB MANUAL EXAMI