HSV type 1 thymidine kinase protein accumulation in round spermatids induces male infertility by spermatogenesis disruption and apoptotic loss of germ cells

• Published in: Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2009, Vol.27 (1), p.14-21
• Main Authors: Cai, Li-yi, Kato, Takako, Nakayama, Michie, Susa, Takao, Murakami, Sanae, Izumi, Shun-ichiro, Kato, Yukio
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Apoptosis - physiology; Biological and medical sciences; Birth control; Embryology: invertebrates and vertebrates. Teratology; Epididymis - enzymology; Epididymis - pathology; Fundamental and applied biological sciences. Psychology; Gynecology. Andrology. Obstetrics; Herpesvirus 1, Human - enzymology; Herpesvirus 1, Human - genetics; HSV-infection; HSV1-TK; Immunohistochemistry; Infertility, Male - enzymology; Infertility, Male - genetics; Male; Medical sciences; Rats; Rats, Inbred F344; Rats, Transgenic; Spermatids - enzymology; Spermatids - pathology; Spermatogenesis; Spermatogenesis - genetics; Spermatozoa - ultrastructure; Sterility. Assisted procreation; Teratology. Teratogens; Testis - enzymology; Testis - pathology; Thymidine Kinase - genetics; Thymidine Kinase - metabolism; Toxicology; Transgenic rat; Viral Structural Proteins - genetics; Viral Structural Proteins - metabolism
• ISSN: 0890-6238; 1873-1708
• DOI: 10.1016/j.reprotox.2008.11.052

HSV type 1 thymidine kinase (HSV1-TK)-introduced transgenic rodents and HSV-infected humans were reported to suffer male infertility. The present study aimed to find novel clues to clarify the cause of HSV1-TK-induced male infertility using an HSV1- tk transgenic rat line. Two truncated HSV1-TK proteins, 37 and 39 kDa, were produced and accumulated in the round spermatids, and their transcription initiation site was identified for the first time at the 65 base downstream of the translation start point of the full-length 43 kDa HSV1-TK. Spermatozoa from those young transgenic rats showed malformed heads, looped tails, and missing cell membrane in heads and tails. Furthermore, age-dependent germ cell loss was observed. TUNEL assay suggested that this germ cell loss is caused by increased apoptotic germ cell death. These results suggest that the expression of HSV1-TK in testes brings about not only abnormal spermiogenesis but also a loss of germ cells due to apoptosis. These findings could provide a novel clue to elucidate the molecular mechanism underlying male infertility in transgenic animals and HSV-infected patients.