4.6 Article

Proliferation and Apoptosis of Cat (Felis catus) Male Germ Cells during Breeding and Non-Breeding Seasons

Journal

VETERINARY SCIENCES
Volume 9, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/vetsci9080447

Keywords

feline; testicle; orchiectomy; spermatogenesis; seasonal breeding

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This study found that cat spermatogenesis is seasonally regulated, with increased spermatogonial proliferation during the reproductive period and increased germ cell apoptosis during the non-reproductive period.
Simple Summary Spermatogenesis is a complex process through which male gametes, spermatozoa, are produced starting from stem germ cells called spermatogonia. The existing information on cat spermatogenesis is limited and somewhat contradictory. In fact, although this species is considered a long-day breeder with a reproduction period starting when the day length increases and ending in late autumn, spermatogenesis and sperm production occur throughout the year. In order to assess whether cat spermatogenesis is modulated according to a season pattern, we analyzed testes taken from feral cats orchiectomized during reproductive (February-July) and non-reproductive (November and December) periods. The results of the analyses carried out in the present study showed that spermatogonial proliferation was more intense during the reproductive period and germ cell death via apoptosis (a programmed form of cell death) increased during the non-reproductive period. Our results confirm the hypothesis that cat spermatogenesis is seasonally modulated through changes of germ cell proliferation and apoptosis, according to a common paradigm of seasonally breeding species. The domestic cat (Felis catus) is a seasonal-breeding species whose reproductive period starts when the day length increases. Since the existing information on cat spermatogenesis is limited and somewhat contradictory, in the present study, germ cell proliferation and apoptosis in feral adult tomcats orchiectomized during reproductive (reproductive group, RG; February-July) and non-reproductive (non-reproductive group, NRG; November and December) seasons were compared. Cross-sections taken from the middle third of the left testis were chemically fixed and embedded in paraffin wax. Histological sections were processed for the immunohistochemical detection of proliferating germ cells (PCNA) and for the identification of apoptotic cells (TUNEL method). The percentage of PCNA-positive spermatogonia was higher in the RG than in the NRG. On the contrary, germ cell apoptosis was higher in the NRG than in the RG. Our results confirm that cat spermatogenesis is modulated on a seasonal basis and suggests that spermatogenesis control involves changes in germ cell proliferation and apoptosis according to a common paradigm of seasonally breeding species.

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