Key Apoptotic Pathways for Heat-Induced Programmed Germ Cell Death in the Testis

Amiya P. Sinha Hikim(UCLA Medical Center), Yanhe Lue(UCLA Medical Center), Cindy M. Yamamoto(UCLA Medical Center), Y. Vera(UCLA Medical Center), Susana Rodriguez(UCLA Medical Center), Pauline H. Yen(University of California, Los Angeles), Kevin Soeng(UCLA Medical Center), Christina Wang(UCLA Medical Center), Ronald S. Swerdloff(UCLA Medical Center)
Endocrinology
April 15, 2003
Cited by 211Open Access
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Abstract

Short-term exposure (43 C for 15 min) of the rat testis to mild heat results within 6 h in stage- and cell-specific activation of germ cell apoptosis. Initiation of apoptosis was preceded by a redistribution of Bax from a cytoplasmic to paranuclear localization in heat-susceptible germ cells. Here we show that the relocation of Bax is accompanied by cytosolic translocation of cytochrome c and is associated with activation of the initiator caspase 9 and the executioner caspases 3, 6, and 7 and cleavage of poly(ADP) ribose polymerase. Furthermore, early in apoptosis, a significant amount of Bax also accumulates in endoplasmic reticulum, as assessed by Western blot analyses of fractionated testicular lysates. In additional studies using the FasL-defective gld mice, we have shown that heat-induced germ cell apoptosis is not blocked, thus providing evidence that the Fas signaling system may be dispensable for heat-induced germ cell apoptosis in the testis. Taken together, these results demonstrate that the mitochondria- and possibly also endoplasmic reticulum-dependent pathways are the key apoptotic pathways for heat-induced germ cell death in the testis.


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