scholarly journals Correction: The m6A mRNA demethylase FTO in granulosa cells retards FOS-dependent ovarian aging

2021 ◽  
Vol 12 (12) ◽  
Author(s):  
Zhong-xin Jiang ◽  
Yi-ning Wang ◽  
Zi-yuan Li ◽  
Zhi-hui Dai ◽  
Yi He ◽  
...  
Reproduction ◽  
2009 ◽  
Vol 138 (5) ◽  
pp. 793-799 ◽  
Author(s):  
Margaret L Walker ◽  
Daniel C Anderson ◽  
James G Herndon ◽  
Lary C Walker

In female squirrel monkeys (Saimiri sciureus), the reproductive period normally extends from ∼2.5 years to the mid-teens. In the present study, we examined the age-associated cytological changes in the ovaries of 24 squirrel monkeys ranging in age from newborn to ∼20 years. We found a significant, age-related decline in the number of primordial follicles, with the most pronounced loss occurring between birth and 5 years. After ∼8 years of age, relatively few primordial follicles were evident in the ovarian sections examined. An unusual feature of the aging squirrel monkey ovary is the emergence of highly differentiated, encapsulated clusters of granulosa cells that increase in size and number, particularly after the age of 8 years. Many of these cells express anti-Müllerian hormone, and, histologically, the clusters resemble granulosa cell tumors in humans. However, granulosa cell clusters (GCCs) are present in both ovaries of all older squirrel monkeys, and they display no obvious signs of malignancy, suggesting that they are a normal feature of ovarian aging in this species. Our findings indicate that reproductive senescence in female squirrel monkeys, as in other primates, involves the inexorable depletion of ovarian follicles. In addition, the consistent appearance of abundant, well-differentiated clusters of granulosa cells in older squirrel monkeys, prior to the cessation of reproduction, suggests that these structures may influence the later stages of reproductive potential in this species. Analysis of GCCs in older squirrel monkeys also could yield insights into the pathophysiology of granulosa cell tumors in humans.


Life Sciences ◽  
2016 ◽  
Vol 162 ◽  
pp. 108-114 ◽  
Author(s):  
Tullia Maraldi ◽  
Elisa Resca ◽  
Alessia Nicoli ◽  
Francesca Beretti ◽  
Manuela Zavatti ◽  
...  

2011 ◽  
Vol 2 (4) ◽  
pp. 333-346 ◽  
Author(s):  
Sharyn Bayne ◽  
He Li ◽  
Margaret E. E. Jones ◽  
Alex R. Pinto ◽  
Michelle van Sinderen ◽  
...  

2015 ◽  
Vol 32 (7) ◽  
pp. 1069-1078 ◽  
Author(s):  
Dongdong Zhang ◽  
Xiaoqian Zhang ◽  
Ming Zeng ◽  
Jihong Yuan ◽  
Mengyuan Liu ◽  
...  

2021 ◽  
Vol 12 (8) ◽  
Author(s):  
Zhong-xin Jiang ◽  
Yi-ning Wang ◽  
Zi-yuan Li ◽  
Zhi-hui Dai ◽  
Yi He ◽  
...  

AbstractMultifunctional N6-methyladenosine (m6A) has been revealed to be an important epigenetic component in various physiological and pathological processes, but its role in female ovarian aging remains unclear. Thus, we demonstrated m6A demethylase FTO downregulation and the ensuing increased m6A in granulosa cells (GCs) of human aged ovaries, while FTO-knockdown GCs showed faster aging-related phenotypes mediated. Using the m6A-RNA-sequence technique (m6A-seq), increased m6A was found in the FOS-mRNA-3′UTR, which is suggested to be an erasing target of FTO that slows the degradation of FOS-mRNA to upregulate FOS expression in GCs, eventually resulting in GC-mediated ovarian aging. FTO acts as a senescence-retarding protein via m6A, and FOS knockdown significantly alleviates the aging of FTO-knockdown GCs. Altogether, the abovementioned results indicate that FTO in GCs retards FOS-dependent ovarian aging, which is a potential diagnostic and therapeutic target against ovarian aging and age-related reproductive diseases.


Endocrinology ◽  
2020 ◽  
Vol 161 (9) ◽  
Author(s):  
Qing He ◽  
Lifang Gu ◽  
Qingyin Lin ◽  
Yi Ma ◽  
Chunlian Liu ◽  
...  

Abstract Mitochondria play important roles in ovarian follicle development. Mitochondrial dysfunction, including mitochondrial gene deficiency, impairs ovarian development. Here, we explored the role and mechanism of mitochondrial inner membrane gene Immp2l in ovarian follicle growth and development. Our results revealed that female Immp2l-/- mice were infertile, whereas Immp2l+/- mice were normal. Body and ovarian weights were reduced in the female Immp2l-/- mice, ovarian follicle growth and development were stunted in the secondary follicle stage. Although a few ovarian follicles were ovulated, the oocytes were not fertilized because of mitochondrial dysfunction. Increased oxidative stress, decreased estrogen levels, and altered genes expression of Wnt/β-catenin and steroid hormone synthesis pathways were observed in 28-day-old Immp2l-/- mice. The Immp2l mutation accelerated ovarian aging process, as no ovarian follicles were detected by age 5 months in Immp2l-/- mice. All the aforementioned changes in the Immp2l-/- mice were reversed by administration of antioxidant melatonin to the Immp2l-/- mice. Furthermore, our in vitro study using Immp2l knockdown granulosa cells confirmed that the Immp2l downregulation induced granulosa cell aging by enhancing reactive oxygen species (ROS) levels, suppressing Wnt16, increasing β-catenin, and decreasing steroid hormone synthesis gene cyp19a1 and estrogen levels, accompanied by an increase in the aging phenotype of granulosa cells. Melatonin treatment delayed granulosa cell aging progression. Taken together, Immp2l causes ovarian aging through the ROS-Wnt/β-catenin-estrogen (cyp19a1) pathway, which can be reversed by melatonin treatment.


Diagnostics ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 295 ◽  
Author(s):  
Pei-Hsuan Lin ◽  
Li-Te Lin ◽  
Chia-Jung Li ◽  
Pei-Gang Kao ◽  
Hsiao-Wen Tsai ◽  
...  

Aging of functional ovaries occurs many years before aging of other organs in the female body. In recent years, a greater number of women continue to postpone their pregnancies to later stages in their lives, raising concerns of the effect of ovarian aging. Mitochondria play an important role in the connection between the aging granulosa cells and oocytes. However, the underlying mechanisms of mitochondrial dysfunction in these cells remain poorly understood. Therefore, we evaluated the molecular mechanism of the aging granulosa cells, including aspects such as accumulation of mitochondrial reactive oxygen species, reduction of mtDNA, imbalance of mitochondrial dynamics, and diminished cell proliferation. Here, we applied bioinformatics approaches, and integrated publicly available resources, to investigate the role of CREB1 gene expression in reproduction. Senescence hallmark enrichment and pathway analysis suggested that the downregulation of bioenergetic-related genes in CREB1. Gene expression analyses showed alterations in genes related to energy metabolism and ROS production in ovary tissue. We also demonstrate that the biogenesis of aging granulosa cells is subject to CREB1 binding to the PRKAA1 and PRKAA2 upstream promoters. In addition, cofactors that regulate biogenesis significantly increase the levels of SIRT1 and PPARGC1A mRNA in the aging granulosa cells. These findings demonstrate that CREB1 elevates an oxidative stress-induced senescence in granulosa cells by reducing the mitochondrial function.


2021 ◽  
Vol 7 (1) ◽  
pp. eabc7409
Author(s):  
José M. Navarro-Pando ◽  
Elísabet Alcocer-Gómez ◽  
Beatriz Castejón-Vega ◽  
Elena Navarro-Villarán ◽  
Mónica Condés-Hervás ◽  
...  

Inflammation is a hallmark of aging and is negatively affecting female fertility. In this study, we evaluate the role of the NLRP3 inflammasome in ovarian aging and female fertility. Age-dependent increased expression of NLRP3 in the ovary was observed in WT mice during reproductive aging. High expression of NLRP3, caspase-1, and IL-1β was also observed in granulosa cells from patients with ovarian insufficiency. Ablation of NLRP3 improved the survival and pregnancy rates and increased anti-Müllerian hormone levels and autophagy rates in ovaries. Deficiency of NLRP3 also reduced serum FSH and estradiol levels. Consistent with these results, pharmacological inhibition of NLRP3 using a direct NLRP3 inhibitor, MCC950, improved fertility in female mice to levels comparable to those of Nlrp3−/− mice. These results suggest that the NLRP3 inflammasome is implicated in the age-dependent loss of female fertility and position this inflammasome as a potential new therapeutic target for the treatment of infertility.


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