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Reproduction (2009) 137 487-495
DOI: 10.1530/REP-08-0358
Copyright © 2009 Society for Reproduction and Fertility
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RESEARCH

Exposure of the mouse perinatal testis to radiation leads to hypospermia at sexual maturity

A Forand1,2,3, S Messiaen1,2,3, R Habert1,2,3 and J Bernardino-Sgherri1,2,3

1 Laboratory of Differentiation and Radiobiology of the Gonads, CEA, DSV, iRCM, SCSR, Fontenay aux Roses F-92265, France2 Unit of Gametogenesis and Genotoxicity, Université Paris 7 Denis Diderot, Fontenay aux Roses F-92265, France3 INSERM, U566, Fontenay aux Roses F-92265, France

Correspondence should be addressed to J Bernardino-Sgherri; Email: jacqueline.bernardino{at}cea.fr

The first round of mouse spermatogenesis begins from 3 to 4 days after birth through differentiation of gonocytes into spermatogonial-stem cells and type A spermatogonia. Consequently, this step of differentiation may determine generation of the original population of stem cells and the fertility potential of the adult mouse. We aimed to determine the effect of perinatal exposure to ionizing radiation on the testis at the end of the first wave of spermatogenesis and at sexual maturity. Our results show that, radiation sensitivity of the testis substantially decreases from late foetal life to the end of the first week after birth. In addition, partial or full recovery from radiation induced testicular weight loss occurred between the first round of spermatogenesis and sexual maturity, and this was associated with the stimulation of spermatogonial proliferation. Exposure of mice at 17.5 days after conception or at 1 day after birth to {gamma}-rays decreased the sperm counts at sexual maturity, while exposure of 8 day-old mice had no effect. This suggests that irradiation of late foetal or early neonatal testes has a direct impact on the generation of the neonatal spermatogonial-stem cell pool.







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