Key result
SIRT1 regulates ovarian granulosa cell function and shares overlapping actions with human chorionic gonadotropin.
Why the study?
This review aims to provide state-of-the-art information on the mode of action and roles of SIRT1 in human granulosa-lutein cells and granulosa cells from other species, and discuss overlapping actions with human chorionic gonadotropin.
This review highlights the role of SIRT1 in female reproduction, specifically its action in granulosa-lutein cells and similarities to human chorionic gonadotropin.
May guide preclinical research on SIRT1 in ovarian function; should not yet change clinical practice in reproductive medicine.
Sirtuin 1 (SIRT1) is a nicotinamide adenine dinucleotide-dependent deacetylase that modifies gene expression through histone deacetylation. It also deacetylates nonhistone substrates, e.g., tumor suppressor p53, NOS3, HIF1A, NFKB, FOXO3a, PGC-1α, and PPARγ. Consequently, it regulates a wide range of physiological functions including cell cycle control, energy expenditure, oxidative stress response, apoptosis, and aging. SIRT1 is expressed in ovarian granulosa cells (GCs) of various species including humans at different stages of the reproductive cycle. The importance of SIRT1 in female reproduction is supported by the findings that SIRT1-knockout mice exhibit defects in reproductive tissue development. These mice were found to have a thin-walled uterus, small ovaries, with follicles present but no corpora lutea. This review aims to provide state-of-the-art information on SIRT1's mode of action and its roles in human granulosa-lutein cells and GCs from other species where data are available. It also discusses the overlapping actions of SIRT1 and human chorionic gonadotropin on the production of critical GC-borne factors.
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Meidan et al. (2023) conducted a review in Female reproduction. Sirtuin 1 (SIRT1) was evaluated. SIRT1 regulates physiological functions in ovarian granulosa cells and shares overlapping actions with human chorionic gonadotropin on the production of critical granulosa cell-borne factors.
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