1997
DOI: 10.1046/j.1365-2265.1997.00157.x
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Physiological cell death in endocrine‐dependent tissues: an ovarian perspective

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Cited by 34 publications
(26 citation statements)
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References 104 publications
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“…It has been postulated that FSH stimulates granulosa cells to secrete IGF-1, which in turn signals thecal cells to produce EGF and TGFα, thereby exerting an antiapoptotic response . In contrast, expression of TGFβ in hormone-deprived follicles may promote apoptosis (Martimbeau and Tilly 1997). Other pro-and antiapoptotic genes have been shown to affect follicular atresia.…”
Section: Ovarymentioning
confidence: 99%
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“…It has been postulated that FSH stimulates granulosa cells to secrete IGF-1, which in turn signals thecal cells to produce EGF and TGFα, thereby exerting an antiapoptotic response . In contrast, expression of TGFβ in hormone-deprived follicles may promote apoptosis (Martimbeau and Tilly 1997). Other pro-and antiapoptotic genes have been shown to affect follicular atresia.…”
Section: Ovarymentioning
confidence: 99%
“…Unlike the male reproductive tissues, however, cyclic endocrine-dependent cell death in these female tissues is a normal physiological process closely linked to the cyclic fluctuations in hormonal secretions (Martimbeau and Tilly 1997). The phases of the female ovarian and menstrual cycles closely correlate with alterations in hormonal levels (Gosden and Spears 1997;Kiess and Gallaher 1998;Martimbeau and Tilly 1997) (Fig.…”
Section: Endocrine Regulation Of Involution In the Ovary And Uterusmentioning
confidence: 99%
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“…Using sensitive biochemical and molecular biological analyses, the occurrence of apoptosis in female germ cells, follicular granulosa cells, and luteal cells during ovarian development and cyclic function in laboratory and domestic animal species has been established (reviewed in Tilly, 1996;Martimbeau and Tilly, 1997). Moreover, identification of apoptosis as the underlying mechanism responsible for controlled cellular deletion in the ovary has sparked numerous investigations into the intracellular effector pathways that are either activated or repressed during execution of the cell death command.…”
Section: Introductionmentioning
confidence: 99%
“…For GO 0015975 (energy deriva- March 2017, pp.64-79, © 2017 tion by oxidation of reduced inorganic compounds), endocrine diseases are related to oxidation of compounds (Olmez-Hanci et al, 2009). GO 0043067 (regulation of programmed cell death) regulates programmed cell death which affects endocrine-dependent tissues (Martimbeau and Tilly, 1997). GO 0031589 (cell-substrate adhesion) attaches a cell to the underlying substrate via adhesion molecules.…”
Section: Feature Analysismentioning
confidence: 99%