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Updated: Aug 14, 2026

A Seminiferous Tubule Squash Technique for the Cytological Analysis of Spermatogenesis Using the Mouse Model
Published on: February 6, 2018
Morphological and quantitative analysis of spermatogonia in mouse testes using whole mounted seminiferous tubules.
Abstract:
In adult male mice exposed to 300 R X-irradiation, the spermatogonial population was selectively killed except for the radioresistant type As stem cells. Type A spermatogonia were minimal two days after irradiation, when only 20% of the control population was present in stage 5-6; these were predominately single and paired undifferentiated cells. When multiple injections of 3HTdR were given between 2 and 3.5 days post-irradiation, 90-95% of these survivors in stages 4-6 became labeled. Enhanced proliferation of these stem cells, and at times when they were normally quiescent, led to restoration of all classes of spermatogonia by 11 days after irradiation. Several autoradiographic studies were undertaken to better characterize the radioresistant cells. In mice given single or multiple injections of 3HTdR prior to irradiation, there was appreciable retention of label by those type As spermatogonia that had originally incorporated 3HTdR in stages 2-4. This labeling pattern was identical to that of the long-cycling As stem cells in nonirradiated testes. Since the long-cycling As stem cells are thought to be characterized by a prolonged G1 or "A-phase" which is known to be a highly radioresistant portion of the cell cycle, it was clear why these cells could preferentially survive irradiation doses that killed other spermatogonial types. It was proposed that following germ cell depletion, as after irradiation injury, the long-cycling As survivors could be prematurely triggered from A-phase into DNA synthesis, thereby, initiating restoration of the germ cell population.
Insights
X-irradiation selectively kills spermatogonia, sparing radioresistant type A stem cells. These stem cells proliferate, restoring the germ cell population after irradiation injury.
Area of Science:
- Reproductive biology
- Radiation biology
- Cell biology
Background:
- Spermatogonial populations are sensitive to radiation, with type A stem cells being an exception.
- Understanding the radioresistance mechanisms of stem cells is crucial for fertility preservation.
Purpose of the Study:
- To identify and characterize radioresistant spermatogonial stem cells after X-irradiation.
- To elucidate the mechanism of germ cell population restoration following radiation damage.
Main Methods:
- Adult male mice were exposed to 300 R X-irradiation.
- 3H-thymidine (3HTdR) was administered via single or multiple injections before and after irradiation.
- Autoradiography was used to track cell populations and proliferation.
Main Results:
- Type A spermatogonia were selectively depleted, with radioresistant stem cells surviving.
- Injected 3HTdR labeled 90-95% of surviving type A spermatogonia (stages 4-6) 2-3.5 days post-irradiation.
- Labeling patterns indicated long-cycling As stem cells, characterized by a radioresistant G1 phase, were responsible for repopulation.
- Germ cell restoration occurred by 11 days post-irradiation.
Conclusions:
- Long-cycling type A spermatogonial stem cells possess inherent radioresistance due to their prolonged G1 phase.
- These stem cells can be prematurely triggered into DNA synthesis to restore the spermatogonial population after radiation-induced depletion.
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