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Updated: Jan 27, 2026

Assessment of Sexual Behavior of Male Mice
Published on: March 5, 2020
Sexual precocity in male microminipigs evaluated immunohistologically using spermatogonial stem cell markers
Julio Almunia1, Kotono Nakamura1, Mami Murakami2
1The United Graduate School of Veterinary Sciences, Gifu University, Japan.
Abstract:
Microminipigs are one of the smallest miniature pigs characterized as sexually precocious; the males achieve sexual maturity at around 3-4.5 months of age. However, the physiology of this sexual precocity is still unclear. To understand sexual precocity in male microminipigs, we analyzed their testes at five developmental stages: neonatal (<7 days), 30-day-old, 45-day-old, 80-day-old, and adult (>24 months) stages. We used 4 pigs in each of the stages. To analyze testicular development histologically, the seminiferous tubule diameter (SD) was measured, and the presence or absence of the seminiferous lumen was confirmed. Changes in the expression of pluripotency markers, DBA, UCHL1, ZBTB16, and vimentin, were evaluated immunohistologically. For the analyses, cells positive for DBA, UCHL1, and ZBTB16 per 150 round seminiferous tubules in cross sections from each testis were counted to evaluate the total number of positive cells. The number of positive cells per 100 Sertoli cells (DBA+/Sertoli, UCHL1+/Sertoli, and ZBTB16+/Sertoli) was calculated to compare the five developmental stages. Histologically, SDs became larger with piglet growth, and precocity was confirmed; seminiferous lumens were observed from the 30-day-old stage. Immunohistologically, the number of DBA+/Sertoli, which indicates the number of gonocytes, decreased rapidly to an undetectable level by the 45-day-old stage. In the same period, the number of UCHL1+/Sertoli, which indicates total SSCs, increased significantly, suggesting that the proliferation of SSCs was accelerated before 30 days of age. Consequently, our study clarified that differentiation of SSCs in microminipigs started during the fetal period, the differentiation of gonocytes and proliferation of SSCs was then accelerated before 30 days of age, and the early phase of spermatogenesis was finally completed at around 45 days after birth. Consequently, sexual precocity in male microminipigs was characterized by a shorter duration of the early phase of spermatogenesis.
Insights
Male microminipigs exhibit sexual precocity due to accelerated spermatogenesis. Their sexual development involves early gonocyte differentiation and rapid stem cell proliferation, completing early spermatogenesis by 45 days. This study clarifies the physiological basis of their early sexual maturity.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Animal Science
Background:
- Microminipigs are known for sexual precocity, reaching maturity early, but the underlying physiological mechanisms remain unclear.
- Understanding the timeline of testicular development and the behavior of key cell populations is crucial for explaining this phenomenon.
Purpose of the Study:
- To investigate the physiological basis of sexual precocity in male microminipigs.
- To analyze testicular development and the expression of key markers during five distinct developmental stages.
Main Methods:
- Histological analysis of seminiferous tubule diameter and lumen presence.
- Immunohistochemical evaluation of pluripotency markers (DBA, UCHL1, ZBTB16) and vimentin.
- Quantification of marker-positive cells relative to Sertoli cells across developmental stages.
Main Results:
- Seminiferous tubule diameter increased with age, and lumens appeared by 30 days.
- Gonocyte markers (DBA) decreased significantly by 45 days.
- Spermatogonial stem cell (SSC) markers (UCHL1) increased significantly before 30 days, indicating accelerated proliferation.
Conclusions:
- SSC differentiation begins prenatally, with accelerated gonocyte differentiation and SSC proliferation occurring before 30 days of age.
- Early spermatogenesis is completed around 45 days post-birth in microminipigs.
- Sexual precocity in male microminipigs is characterized by a significantly shortened duration of the early spermatogenesis phase.
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