Robo1/2 regulate follicle atresia through manipulating granulosa cell apoptosis in mice
Jiangchao Li1, Yuxiang Ye1, Renli Zhang2
1Institute of Vascular Biological Sciences, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Abstract:
Secreted Slit proteins and their Roundabout (Robo) receptors act as a repulsive cue to prevent axons from migrating to inappropriate locations during the development of the nervous system. Slit/Robo has also been implicated in reproductive system development, but the molecular mechanism of the Slit/Robo pathway in the reproductive system remains poorly understood. Using a transgenic mouse model, we investigated the function of the Slit/Robo pathway on ovarian follicle development and atresia. We first demonstrated that more offspring were born to mice with a partial knockout of the Robo1/2 genes in mice. We next showed that Robo1 and Robo2 are strongly expressed in ovarian granulosa cells. Apoptosis in granulosa cells was reduced when Robo1/2 were partially knocked out, and this observation was further verified by in vitro Robo1/2 knockout experiments in mouse and human granulosa cells. We also found that ovarian angiogenesis was enhanced by a partial lack of Robo1/2 genes. In summary, our data suggest that the Slit/Robo pathway can impact follicle development and atresia by influencing granulosa cell apoptosis.
Insights
The Slit/Robo pathway regulates ovarian follicle development. Inhibiting Roundabout (Robo) 1/2 genes reduced granulosa cell apoptosis and enhanced ovarian angiogenesis, leading to more offspring.
Area of Science:
- Reproductive biology
- Developmental neuroscience
Background:
- Secreted Slit proteins and Roundabout (Robo) receptors guide neuronal development.
- The Slit/Robo pathway's role in reproductive system development is not well understood.
Purpose of the Study:
- Investigate the function of the Slit/Robo pathway in ovarian follicle development and atresia using a mouse model.
Main Methods:
- Generated transgenic mice with partial Robo1/2 gene knockout.
- Examined ovarian follicle development, granulosa cell apoptosis, and angiogenesis.
- Conducted in vitro knockout experiments on mouse and human granulosa cells.
Main Results:
- Partial Robo1/2 knockout mice had increased offspring.
- Robo1 and Robo2 are highly expressed in ovarian granulosa cells.
- Reduced granulosa cell apoptosis and enhanced ovarian angiogenesis were observed in Robo1/2 partial knockout mice.
Conclusions:
- The Slit/Robo pathway influences ovarian follicle development and atresia.
- This regulation occurs via modulation of granulosa cell apoptosis and ovarian angiogenesis.


