There are three subtypes of spermatogonia in humans:
- Type A (dark) cells, with dark nuclei. These cells are reserve spermatogonial stem cells which do not usually undergo active mitosis.
- Type A (pale) cells, with pale nuclei. These are the spermatogonial stem cells that undergo active mitosis. These cells divide to produce Type B cells.
- Type B cells, which undergo growth and become primary spermatocytes.
Anticancer drugs such as doxorubicin and vincristine can adversely affect male fertility by damaging the DNA of proliferative spermatogonial stem cells. Experimental exposure of rat undifferentiated spermatogonia to doxorubicin and vincristine indicated that these cells are able to respond to DNA damage by increasing their expression of DNA repair genes, and that this response likely partially prevents DNA break accumulation. In addition to a DNA repair response, exposure of spermatogonia to doxorubicin can also induce programmed cell death (apoptosis).
- Mahla, R.S. "Spermatogonial Stem Cells (SSCs) in Buffalo (Bubalus bubalis) Testis". PLOS ONE. doi:10.1371/journal.pone.0036020. PMC 3334991.
- Beaud H, van Pelt A, Delbes G (2017). "Doxorubicin and vincristine affect undifferentiated rat spermatogonia". Reproduction. 153 (6): 725–735. doi:10.1530/REP-17-0005. PMID 28258155.
- Habas K, Anderson D, Brinkworth MH (2017). "Germ cell responses to doxorubicin exposure in vitro" (PDF). Toxicol. Lett. 265: 70–76. doi:10.1016/j.toxlet.2016.11.016. PMID 27890809.
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