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Updated: Oct 7, 2025

Using Ex Vivo Upright Droplet Cultures of Whole Fetal Organs to Study Developmental Processes during Mouse Organogenesis
Published on: October 21, 2015
Role of mesonephric contribution to mouse testicular development revisited
Gerald R Cunha1, Mei Cao1, Sena Aksel1
1Department of Urology, University of California, 400 Parnassus Avenue, San Francisco, CA, 94143, USA.
Abstract:
The role of the mesonephros in testicular development was re-evaluated by growing embryonic day 11.5 (E11.5) mouse testes devoid of mesonephros for 8-21 days in vivo under the renal capsule of castrated male athymic nude mice. This method provides improved growth conditions relative to previous studies based upon short-term (4-7 days) organ culture. Meticulous controls involved wholemount examination of dissected E11.5 mouse testes as well as serial sections of dissected E11.5 mouse testes which were indeed shown to be devoid of mesonephros. As expected, grafts of E11.5 mouse testes with mesonephros attached formed seminiferous tubules and also contained mesonephric derivatives. Grafts of E11.5 mouse testes without associated mesonephros also formed seminiferous tubules and never contained mesonephric derivatives. The consistent absence of mesonephric derivatives in grafts of E11.5 mouse testes grafted alone is further proof of the complete removal of the mesonephros from the E11.5 mouse testes. The testicular tissues that developed in grafts of E11.5 mouse testes alone contained canalized seminiferous tubules composed of Sox9-positive Sertoli cells as well as GENA-positive germ cells. The seminiferous tubules were surrounded by α-actin-positive myoid cells, and the interstitial space contained 3βHSD-1-positive Leydig cells. Grafts of E11.5 GFP mouse testes into wild-type hosts developed GFP-positive vasculature indicating that E11.5 mouse testes contain vascular precursors. These results indicate that the E11.5 mouse testis contains precursor cells for Sertoli cells, Leydig cells, myoid cells and vasculature whose development and differentiation are independent of cells migrating from the E11.5 mesonephros.
Insights
The embryonic mouse testis can develop Sertoli, germ, Leydig, and myoid cells, as well as vasculature, independently of the mesonephros. This study confirms the self-sufficiency of early testicular development in mice.
Area of Science:
- Developmental Biology
- Reproductive Biology
- Cell Biology
Background:
- The mesonephros has been historically considered crucial for early testicular development.
- Previous studies were limited by short-term organ culture methods.
- A re-evaluation of the mesonephros' role is necessary using improved techniques.
Purpose of the Study:
- To investigate the role of the mesonephros in embryonic testicular development.
- To determine if testicular cell types can develop independently of mesonephric contribution.
- To assess the self-sufficiency of early mouse testicular development.
Main Methods:
- Embryonic day 11.5 (E11.5) mouse testes were grafted in vivo under the renal capsule of castrated male athymic nude mice.
- Testes were grown for 8-21 days, with and without the associated mesonephros.
- Meticulous controls included wholemount and serial section examination to confirm mesonephros removal.
Main Results:
- Grafts of testes with mesonephros formed seminiferous tubules and contained mesonephric derivatives.
- Grafts of testes without mesonephros also formed seminiferous tubules and lacked mesonephric derivatives.
- Developed testicular tissues included Sox9-positive Sertoli cells, GENA-positive germ cells, α-actin-positive myoid cells, and 3βHSD-1-positive Leydig cells.
- Vascular precursors were identified within E11.5 testes, independent of the mesonephros.
Conclusions:
- The E11.5 mouse testis contains all necessary precursor cells for Sertoli, germ, myoid, and Leydig cell differentiation.
- Testicular vasculature also originates from precursors within the E11.5 testis.
- Testicular development and differentiation at E11.5 are independent of cell migration from the mesonephros.
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