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X‐irradiation–induced changes in the progression of type B spermatogonia and preleptotene spermatocytes
Author(s) -
West A.,
Lähdetie J.
Publication year - 2001
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/1098-2795(200101)58:1<78::aid-mrd11>3.0.co;2-j
Subject(s) - biology , mitosis , somatic cell , meiosis , cell cycle , microbiology and biotechnology , germ cell , cell cycle checkpoint , apoptosis , dna damage , immunology , genetics , dna , gene
In response to induced DNA damage, proliferating cells arrest in their cell cycle or go into apoptosis. Ionizing radiation is known to induce degeneration of mammalian male germ cells. The effects on cell‐cycle progression, however, have not been thoroughly studied due to lack of methods for identifying effects on a particular cell‐cycle phase of a specific germ cell type. In this study, we have utilized the technique for isolation of defined segments of seminiferous tubules to examine the cell‐cycle progression of irradiated rat mitotic (type B spermatogonia) and meiotic (preleptotene spermatocytes) G1/S cells. Cells irradiated as type B spermatogonia in mitotic S phase showed a small delay in progression through meiosis. Thus, it seems that transient arrest in the progression can occur in the otherwise strictly regulated progression of germ cells in the seminiferous epithelium. Contrary to the arrest observed in type B spermatogonia and in previous studies on somatic cells, X‐irradiation did not result in a G1 delay in meiotic cells. This lack of arrest occurred despite the presence of unrepaired DNA damage that was measured when the cells had progressed through the two meiotic divisions. Mol. Reprod. Dev. 58:78–87, 2001. © 2001 Wiley‐Liss, Inc.