Morphological and quantitative analysis of spermatogonia in mouse testes using whole mounted seminiferous tubules.

The Anatomical Record
|December 1, 1978
PubMed

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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