P21 super((Cip1/WAF1)) expression in the mouse testis before and after X irradiation

• Published in: Molecular reproduction and development Vol. 47; no. 3; pp. 240 - 247
• Main Authors: Beumer, T L, Roepers-Gajadien, H L, Gademan, I S, Rutgers, D H, De Rooij, DG
• Format: Journal Article
• Language: English
• Published: 01.07.1997
• ISSN: 1040-452X

During spermatogenesis, the radiosensitivity of testicular cells changes considerably. To investigate the molecular mechanisms underlying these radiosensitivity differences, p21 super((Cip1/WAF1)) expression was studied before and after irradiation in the adult mouse testis. P21 super((Cip1/WAF1)) is a cyclin-dependent kinase inhibitor (CDI) and has a role in the G1/S checkpoint and differentiation. P21 super((Cip1/WAF1)) expression was observed in the normal testis, using Western blotting analysis. After a dose of 4 Gy, but not after 0.3 Gy, an increase in p21 super((Cip1/WAF1)) expression could be determined in whole testis lysates. To investigate which germ cells are involved in p21 super(Cip1/WAF1)) protein expression, immunohistochemical analysis was performed on irradiated testis. In the normal testis a weak staining for p21 super(Cip1/WAF1)) was found in pachytene spermatocytes in epithelial stage V up to step 5 spermatids. A dose of 4 Gy of X-irradiation resulted in a transient increase of p21 super((Cip1 /WAF1)) staining in these cells with a maximum at 6 hr post irradiation, despite the fact that the irradiation did not induce an increase in the number of apoptotic spermatocytes. When a dose of 0.3 Gy was given, no increase in p21 super((Cip1/WAF1)) staining was observed. Using the TUNEL technique, a 10-fold increase in apoptotic spermatogonia was found after a dose of 4 Gy. However, no staining for p21 super((Cip1/WAF1)) was observed in spermatogonia, suggesting that these cells do not undergo a p21 super((Cip1 /WAF1))-induced G1 arrest prior to DNA repair or apoptosis. These data imply that p21 super((Cip1/WAF1)) is a factor which could be important during the meiotic prophase in spermatocytes and repair mechanisms in these cells, but not in spermatogonial cell cycle delay or apoptosis induction.