4.7 Article

Increased sperm chromatin decondensation in selected nonapoptotic spermatozoa of patients with male infertility

Journal

FERTILITY AND STERILITY
Volume 92, Issue 2, Pages 572-577

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.fertnstert.2008.07.1705

Keywords

Hamster oocyte; ICSI; human sperm; apoptosis; annexin V

Funding

  1. German Research Council (Deutsche Forschungsgemeinschaft, DFG) [GL 199/4]
  2. Faculty of Medicine, University of Leipzig

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Objective: To evaluate the sperm chromatin decondensation (SCD) rates of the annexin-negative (nonapoptotic) sperm fraction of patients with infertility using hamster intracytoplasmic sperm injection (H-ICSI). In healthy donors, the depletion of apoptotic sperm using annexin V-based magnetic-activated cell separation (MACS) enhances hamster oocyte sperm penetration but does not increase SCD rates following H-ICSI. Design: A prospective-controlled study. Setting: Male infertility clinic, European Academy of Andrology Center Leipzig. Patient(s): Twenty-one male infertility patients with subnormal spermiogram. Intervention(s): Spermatozoa were separated by Annexin V-MACS. Main Outcome Measure(s): Apoptosis signaling (disruption of transmembrane mitochondrial potential, transmembrane mitochondrial potential [TMP], and activation of caspases-3 [CP3]) and SCD rates of human spermatozoa after hamster intracytoplasmic sperm injection. Result(s): Infertility patients showed high levels of sperm with active CP3 and disrupted TMP, which correlated negatively with SCD rates. Annexin V-MACS resulted in a significant enrichment of spermatozoa with inactive CP3 and intact TMP in the annexin-negative fraction. Similarly, annexin-negative sperm had the highest SCD rates following H-ICSI compared with controls and annexin-positive sperm. Conclusion(s): These results suggest that nonapoptotic spermatozoa prepared by annexin V-MACS display higher early fertilization potential following ICSI. The technique should be evaluated in a clinical setting for its impact on ICSI outcomes in patients diagnosed with infertility. (Fertil Steril (R) 2009;92:572-7. (C) 2009 by American Society for Reproductive Medicine.)

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