Scientific Reports · 2016 · 22 citations · 32 references
Life SciencesCell BiologyMolecular BiologyApoptosisChromatin StructureEpigeneticsChromatinHistone ModificationsHistone ProteinsOocyte MaturationOogenesisOvarian PhysiologyChromatin ConfigurationEpigenetic MarksHistone AcetylationHistone-lysine AcetylationOocyte Chromatin RemodelingOocyte DevelopmentOocyte PreservationOvarian Apoptosis
The epigenetic factors causing competence differences between SN (surrounded nucleolus) and NSN (non-surrounded nucleolus) oocytes, the significance for the increased histone acetylation and methylation in SN oocytes, and whether chromatin configuration or histone modification determines oocyte competence, are unclear. This study has addressed these issues by using the ovary-holding (OH) stress models where oocyte SN configuration was uncoupled from histone modifications and developmental potential. Prepubertal mouse ovaries containing high percentages of NSN oocytes were preserved at 37 or 39 °C for 1 or 2 h before examination for oocyte chromatin configuration, developmental competence, histone modification and apoptosis. Whereas 1-h OH at 37 °C caused a moderate apoptosis with increased oocyte competence, improved histone modification and a normal NSN-to-SN transition, harsher OH conditions induced a severe apoptosis with decreased oocyte competence, impaired histone modification and a pseudo (premature) NSN-to-SN transition. Observations on Fas/FasL expression and using the gld (generalized lymphoproliferative disorder) mice harboring FasL mutations indicated that OH triggered oocyte apoptosis with activation of the Fas signaling. It was concluded that OH stress caused oocyte apoptosis with activation of the Fas/FasL system and that oocyte competence was more closely correlated with histone modification than with chromatin configuration.
32
Autocrine T-cell suicide mediated by APO-1/(Fas/CD95)
Jens Dhein, Henning Walczak, Caroline Bäumler et al. · Nature · 1995 · 1.6K citations
Generalized lymphoproliferative disease in mice, caused by a point mutation in the fas ligand
Tomohiro Takahashi, Masato Tanaka, Camllynn I. Brannan et al. · Cell · 1994 · 1.5K citations
Life Sciences, Immunology, Pathology +12
Fas(CD95)/FasL interactions required for programmed cell death after T-cell activation
S T Ju, D J Panka, Haili Cui et al. · Nature · 1995 · 1.5K citations