Phosphatidylserine translocation in human spermatozoa from impaired spermatogenesis

被引:14
作者
Almeida, C. [1 ]
Sousa, M. [1 ,2 ,3 ]
Barros, A. [1 ,2 ]
机构
[1] Univ Porto, Fac Med, Dept Genet, P-4200319 Oporto, Portugal
[2] Ctr Reprod Genet Alberto Barros, P-4100009 Oporto, Portugal
[3] Univ Porto, Cell Biol Lab, ICBAS Inst Biomed Sci Abel Salazar, P-1099003 Oporto, Portugal
关键词
anejaculation; annexin-V; azoospermia; human sperm apoptosis; oligozoospermia; GERM-CELL APOPTOSIS; PLASMA-MEMBRANE TRANSLOCATION; HUMAN SPERM; DNA FRAGMENTATION; TESTICULAR SPERMATOZOA; EFFICIENT TREATMENT; MATURATION ARREST; OXIDATIVE STRESS; SERTOLI-CELLS; SEMEN QUALITY;
D O I
10.1016/j.rbmo.2009.10.002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The aim of the present study was to evaluate phosphatidylserine translocation in specific patient groups and compare the rates of apoptosis between ejaculated and testicular spermatozoa. Fifty-six patients undergoing infertility treatments were included in the present study. Semen samples (n = 37) were obtained from cases with normozoospermia (it = 9) and abnormal semen parameters (n = 28). Testicular biopsy was performed in 19 patients, eight with obstructive and six with non-obstructive (hypospermatogenesis) azoospermia, and in five patients without azoospermia (anejaculation and oligozoospermia). Phosphatidylserine externalization was assessed using annexin-V binding and fluorescence microscopy, and propidium iodide exclusion tests were used to distinguish live from dead cells. In semen, oligoasthenoteratozoospermia showed significantly increased rates of sperm apoptosis (60.3 +/- 12.9) than normozoospermia (47.5 +/- 10.2). In testis, hypospermatogenesis (63.3 +/- 10.3) and obstructive azoospermia (63.6 +/- 15.1) showed significantly increased rates of sperm apoptosis than non-azoospermic patients (49.6 +/- 25.5). Comparisons between semen and testis showed that oligozoospermia had significantly higher rates of sperm apoptosis in semen (57.9 +/- 11.9) than in testis (29.4 +/- 1.1). The results suggest the presence of a post-testicular apoptotic induction factor and the potential beneficial use of testicular spermatozoa in clinical treatments.
引用
收藏
页码:770 / 777
页数:8
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