{"paper_id":"7f0e6a40-74fc-44d0-8ba0-3dbc23af4acf","body_text":"Sirtuins (silent information regulator proteins) were initially defined as an evolutionarily conserved family of class III nicotinamide adenine dinucleotide+ (NAD+)-dependent histone deacetylases that can also have mono-ADP-ribosyltransferase activity [ 1 , 2 ]. These enzymes cleave an acetyl group from acetyl-lysine residues in histones, although they can also act in nonhistone proteins, such us structural proteins, metabolic enzymes or transcriptional factors [ 1 , 2 ]. However, recent studies demonstrate that sirtuin family gene products catalyze additional reactions and enzymatic activities, including mono-ADP-ribosyltransferase, deacylase, deacetylase, desuccinylase, demalonylase, demyristoylase and depalmitoylase activities [ 2 , 3 , 4 ].\nSirtuins are implicated in aging, oxidative stress, maintenance of metabolic homeostasis, DNA repair and mitochondrial function [ 5 , 6 ] through the regulation of specific genes’ expression and activation or deactivation of other proteins [ 7 , 8 ].\nIn mammals, seven sirtuin isoforms have so far been described ( SIRT1 – SIRT7 ). These possess a conserved catalytic domain but differ in their amino and carboxyl terminal that confers specificity in cellular location and function [ 9 ].\nSIRT1  is the most studied member of the sirtuin family, it is located mainly in the nucleus, although it shuttles to the cytosol in response to environmental signals [ 10 ].  SIRT1  has been implicated in processes such as inflammation, by reducing NF-κB activity [ 11 , 12 ], apoptosis by inhibiting p53-dependent transcription [ 13 , 14 ] and in energy metabolism through effects on regulators of metabolic enzymes such as PPAR-γ [ 15 ]. Yeast Sir2 gene is a  SIRT1  homolog that is involved in yeast life span extension, nonetheless, but a similar role for  SIRT1  has been refuted [ 16 ]. In the reproductive system,  SIRT1  plays a role in apoptosis of granulosa cells during follicular atresia [ 17 , 18 ] and has been related to preservation of follicular reserve and extension of ovarian lifespan [ 19 ].\nSIRT2  is located in the cytoplasm [ 9 ]. It transiently migrates into the nucleus to deacetylate α-tubulin and to modulate chromatin condensation and cell cycle regulation by deacetylating H3 and H4 histones [ 20 , 21 ].  SIRT2  deacetylates transcriptional factors like Foxo, p53 or NF-κB [ 4 , 22 , 23 , 24 ].\nSIRT3  resides in the mitochondria [ 9 ] and participates in the regulation of energy metabolism [ 25 , 26 ] and apoptosis [ 27 ] and in reactive oxygen species (ROS) detoxification [ 28 , 29 ].  SIRT3  has been involved in age-associated oxidative stress and infertility [ 30 , 31 , 32 ].\nSIRT4  located in the mitochondria [ 9 ] regulates lipid metabolism promoting fatty acid oxidation and inhibiting lipogenesis [ 33 , 34 ]. The effects of  SIRT3  and  SIRT4  on glutamate dehydrogenase are opposite: while  SIRT4  represses GDH activity, deacetylation by  SIRT3  activates GDH [ 35 , 36 ].\nSIRT5  in mitochondria [ 9 , 37 ] has been reported to possess low deacetylase activity compared to the other members of the family. In contrast,  SIRT5  possesses high desuccinylation, demalonylation and deglutarylation activities [ 4 ]. It activates the urea cycle by deacetylating carbamoyl phosphate synthetase 1 [ 38 ].  SIRT5  desuccinylates isocitrate dehydrogenase 2 and deglutarylates glucose-6-phosphate dehydrogenase, which protect cells from oxidative damage by activating NADPH-producing enzymes [ 39 ]. In women,  SIRT5  expression decreases along with ovarian reserve as maternal age increases [ 40 ].\nSIRT6 , nuclear [ 10 ], is implicated in telomeres stabilization, DNA double strand break repair and regulation of transcription [ 41 , 42 , 43 , 44 ].  SIRT6  overexpression increases lifespan in male mice by ~15% [ 45 ]. Regarding fertility,  SIRT6  has been associated with follicle reserve preservation and increase of ovarian function lifespan [ 19 ].\nSIRT7 , predominantly localized in the nucleolus [ 9 ], co-activates ribosomal DNA transcription by association with RNA polymerase I complex [ 46 , 47 ]. In addition,  SIRT7  interacts with chromatin remodeling complexes by association and deacetylation of the B-WICH component [ 48 ] and plays a role in stress resistance to hypoxia, osmotic stress, ER-stress or genomic stress [ 49 , 50 , 51 ].\nThe aim of this study was to investigate the expression of the genes coding for the 7 sirtuins in human granulosa–lutein (hGL) cells from in vitro fertilization (IVF) patients with different infertility diagnoses, aging women and oocyte donors (young controls) in order to seek differences in gene expression levels and possible correlation with clinical parameters.\n\nSignificant differences in age distribution were found between OD (oocyte donors between 18 and 27 yo) and all other groups ( p  = 0.000) and between ≥40 yo (women ≥ 40 yo with tubal or male factor and no ovarian factor) and all other groups ( p  = 0.000). No age difference was observed between NOF (women between 27 and 39 yo with tubal or male factor and no ovarian factor), PCOS (polycystic ovarian syndrome), EM (endometriosis) and PR (women < 40 yo defined as poor responders) ( Table 1 ).\nWhile agonist and antagonist protocols were differently represented between diagnostic groups, within each group there were no statistically significant differences in gene expression between the 2 protocols.\nRegarding the amount of exogenous gonadotropins used for ovulation induction, PCOS, OD and NOF groups received significantly lower doses compared to EM, PR and ≥40 yo ( p  = 0.000). The number of total and mature oocytes retrieved varied between groups: significant differences are shown in  Table 1 . No statistically significant differences in mean E2 peak value were observed among groups.\nAll sirtuin family members were expressed in human granulosa-lutein cells,  Table 2 .  SIRT1  and  SIRT2  were the most expressed.  SIRT3 ,  SIRT5  and  SIRT7  showed an intermediate expression and  SIRT4  and  SIRT6  the least expression.\nComparing expression between different IVF diagnostic groups gene expression was higher in ≥40 yo patients than in other groups for  SIRT1  (OD:  p  = 0.008; NOF:  p  = 0.000),  SIRT2  (OD:  p  = 0.000; NOF:  p  = 0.000) and  SIRT5  (OD:  p  = 0.032; NOF:  p  = 0.014). With the exception of  SIRT2  and  SIRT7  the NOF group did not differ from the controls,  Figure 1 .\nSirtuins and age—When all women with no ovarian factor (OD, NOF and ≥40 yo) were analyzed, we observed that only  SIRT2 ,  SIRT5  and  SIRT7  expression correlated with age (r = 0.350,  p  < 0.01; r = 0.324,  p  < 0.05 and r = 303,  p  < 0.05) ( Figure 2 ).\nSirtuins and IVF parameters—When different groups were analyzed, no correlation was found between NOF or ≥40 yo with any IVF parameters. The ovum donor controls showed a negative correlation between  SIRT2 ,  SIRT3 ,  SIRT4  and  SIRT6  and administered gonadotrophin doses ( p  < 0.01) and a negative correlation between  SIRT7  and FSH doses ( p  < 0.05). In addition,  SIRT2 ,  SIRT4 ,  SIRT6 ,  SIRT7  expression also correlated negatively with total treatment days ( p  < 0.05).\nComparing expression between different groups ( Table 2 ), no significant difference was observed in  SIRT1  and  SIRT4  gene expression level among any group. Expression levels of  SIRT2  were statistically higher in EM ( p  = 0.000), PR ( p  = 0.000) and PCOS ( p  = 0.010) patients compared to NOF. However, PR present the higher expression level, statistically different from PCOS ( p  = 0.008), while EM has an intermediary value that did not differ from any other group,  Figure 3 .  SIRT3 ,  SIRT5  and  SIRT7  gene expression was statistically higher in PR than in NOF ( p  = 0.029;  p  = 0.011;  p  = 0.003). PCOS and EM present an intermedia expression value that did not differ from NOF or PR ( Figure 3 ).  SIRT6  expression was statistically higher in PR patients than in all other groups (NOF:  p  = 0.002; EM:  p  = 0.045; PCOS:  p  = 0.008) ( Figure 3 ).\nWhen different diagnostic groups were analyzed, we observed that in PR, ≥40 yo and PCOS groups no correlation was found between sirtuin gene expression and gonadotrophin doses. Only in EM patients did  SIRT1 ,  SIRT6  and  SIRT7  correlate positively with FSH and LH doses administered. Interestingly, these correlations with  SIRT6  and  SIRT7  were opposite to those found in control OD.\nWith the exception of a negative correlation for  SIRT4  in PCOS patients, no correlations were found between sirtuin expression and number of days of treatment in the analyzed groups.\nThere was a positive correlation between mitochondrial sirtuins and mature oocytes retrieved in PR patients.\n\nIn view of their NAD+ dependence [ 51 ], there may be a role for sirtuins in intrafollicular cell redox balance and antioxidant response.\nThis article reports the expression levels of the seven sirtuin genes presently known in post-ovarian stimulation and human chorionic gonadotrophin treated human hGL cells and establishes correlations among sirtuin gene expression and clinical status: age, clinical diagnosis, specific ovulation induction and response to treatment;  Table 1 . Notably, the average estradiol level in the PR group is relatively elevated. We defined PR based on the Bologna criteria [ 52 ], but excluding the advanced maternal age subjects, which represent a separate group in our study. The stimulation protocol was adjusted to furnish satisfactory serum estradiol levels prior to hCG injection. We used an antagonist protocol with high doses of LH and FSH based on the expected poor response and the high estradiol levels obtained in some patients probably reflect the high dose of LH used for ovulation induction. Interestingly, our group of poor responders does not include patients >40; the patients’ age range is 28–39, which may have positively affected the ability of granulosa cells to produce estrogen. Our results are in agreement with the paper by Ku et al. [ 53 ], which showed higher estradiol levels in patients treated with a combination of FSH and LH. However, Ku el al. used an ultralong protocol, which may be responsible for lower estradiol levels in their patients.\nIVF patients with no ovarian factor (OD, NOF and ≥40 yo) showed a direct correlation between their hGL cell sirtuin 2, 5 and 7 gene expression and age. This could be a means of maintenance of energy homeostasis, glucose metabolism and reactive oxygen species detoxification, DNA repair and other cell repair mechanism that decrease with age and could result is poor response to ovarian stimulation and compromised oocytes [ 54 , 55 ].\nThe positive correlation of  SIRT2  expression levels with age ( p  < 0.01) in women with no ovarian factor shows a pronounced increase at 40 years old, as shown in  Figure 2  scatter plot. The expression levels of  SIRT2  in the PR and EM groups of patients resemble those of ≥40 yo women,  Table 2 . The higher expression levels of  SIRT2  gene in women older than 40 yo than in the OD and NOF groups supports the hypothesis that  SIRT2  expression increases most notably after forty years [ 56 , 57 , 58 ], always within the age limits or our study.\nSummary —Taken together, these findings imply a feedback loop that induces sirtuin 2, 5 and 7 expression with (ovarian) aging and in relation to disease states that foster the presence of reactive oxygen species in or around the ovary. However, these descriptive studies were not designed to test such relationships.\nFertility decreases from age 35 and reaches a clinically perilous point in most women by age 40. In our study,  SIRT1  gene expression levels were higher in women older than 40 yo than in OD and NOF patients ( Figure 1 ). These data are in agreement with those of Di Emidio et al. [ 30 ], who reported higher levels of  SIRT1  mRNA in aged mouse oocytes and a decreased ability to react to H 2 O 2  addition as a sign of increased oxidative stress (OS). This coincides well with the increase of  SIRT1  expression in response to age dependent OS. A direct correlation between aging and OS increase has been reported with aging-related decay of fertility [ 59 ], and our laboratory reported an increased expression levels of the oxidative stress response gene ALDH3A2 in granulosa-lutein cells that is related to age and infertility diagnosis [ 60 , 61 ].\nSIRT5  gene expression level is significantly higher in ≥40 yo than in OD and NOF ( p  = 0.045 and  p  = 0.010, respectively).  SIRT5 , localized in the mitochondrial matrix, regulates mitochondrial activity and function [ 62 ] by succinylating [ 63 ] or acetylating proteins such as cytochrome C, which is pivotal in oxidative metabolism and the apoptosis processes [ 36 ].\nThese studies closely link sirtuins to the aging ovary. The increase in expression of  SIRT5  gene in women older than 40 years old could represent a feedback loop that is related to the presence of oxidative species.\nOther studies of the sirtuin family and the ovary —There have been other studies of  SIRT5  in human granulosa-lutein cells. Pacella-Ince et al. [ 40 ] reported a lower gene expression level in women of advanced maternal age and reduced ovarian reserve compared to younger women, which is apparently opposite to our results. However, in the article by Pacella-Ince et al., the patients’ distributions within each age group include no ovarian factor women as well as different infertility diagnoses. Furthermore, the different infertility diagnoses are not represented in all groups and percentages among them are notably variable; as a result, the amount of  SIRT5  gene expression given is not specific for age, but just an average of the combined groups [ 40 ].\nWhile convincing of differences in mural hGL cells, these findings do not reveal sirtuin family expression in the cumulus cells that are directly in apposition to the oocyte/embryo. We have shown that there are important biochemical differences between mural and cumulus cells [ 64 , 65 ]. Additionally, there have been reports of miRNA differences in poor responders [ 66 ] and other genes’ expression in cumulus cells from obese women [ 67 , 68 ]; the possibility of mural vs. cumulus differences is on the list for further study.\nSummary— The human ovarian follicle, represented by post-ovulatory luteinized granulosa cells, expresses all known members of the sirtuin family of genes. We have proposed a feedback mechanism related to the presence of inflammation/reactive oxygen species/aging that drives expression of sirtuins as a defensive/protective mechanism.  SIRT6  and  SIRT7  functions include regulation of DNA-repair mechanisms [ 43 , 44 , 50 , 69 ]. The overexpression of  SIRT6  and  SIRT7  in the PR group of patients might be indicative of the role of these sirtuins in an attempt to repair accumulated damage to DNA caused by a deficient response to cellular genotoxic stress [ 45 , 69 ]. However, in NOF and ≥40 yo, the expression levels of these sirtuins do not differ from those observed in younger women (OD) ( Table 2 ). This suggests that in PR the DNA damage is mainly due to genomic instability and not affected by aging [ 54 ]. In the case of patients suffering from EM or PCOS, the slight increase expression of  SIRT7  gene observed may be an effect of incorrect balance between redox response mechanisms and the higher oxidative stress described for these pathologies.\nThe diverse expression patterns of sirtuins among groups reveals not only a clinical, diagnosis-specific profile, but also an age dependent feature.  Figure 4  presents a scheme of alterations and proposed compensatory responses by sirtuin expression in aging and in environmental and metabolic circumstances reflecting pathological and physiological conditions.\n\nUnder a protocol approved by the Ethics Committee of the Universidad de La Laguna, women undergoing ovulation induction for oocyte donation or IVF consented to join this study. Upon reaching the target follicle sizes and receiving 250 µg of hCG, the harvesting of oocytes was by standard methods, see below. After removal of the oocyte from the petri dish, the accompanying mural granulosa-lutein cells were set aside for evaluation, see below. Clinical information included the doses of exogenous follicle stimulating hormone (FSH) and luteinizing hormone (LH) administered, and IVF parameters related to ovarian response to ovulation induction (number of total and mature oocytes retrieved, estradiol concentration on the last day of stimulation, and total number of days of stimulation).\nFifty-six women between 18 and 44 years of age (yo) with no ovarian factor were grouped as: women between 27 and 39 yo with tubal or male factor and no ovarian factor (NOF;  n  = 24); women ≥40 yo with tubal or male factor and no ovarian factor (≥40 yo;  n  = 15); and oocyte donors between 18 and 27 yo (OD,  n  = 17).\nSeventy-four patients were grouped as being between 27 and 39 yo with tubal or male factor and no ovarian factor (NOF;  n  = 24); women <40 yo defined as poor responders according to the European Society of Human Reproduction and Embryology (ESHRE) criteria [ 52 ] (PRs;  n  = 16); women with American Society for Reproductive Medicine (ASRM) [ 70 ] stages III and IV endometriosis, with histologic diagnosis (EM;  n  = 18); polycystic ovarian syndrome (PCOS;  n  = 16) was defined according to the Rotterdam criteria [ 71 ]. Patient demographics and the most relevant clinical characteristics of these sub-groups are shown in  Table 1 .\nOvarian stimulation was carried out with an agonist or antagonist protocol using recombinant FSH (Gonal F, Serono, Madrid, Spain), combined with recombinant LH (Luveris, Serono, Madrid, Spain) or human menopausal gonadotropins (hMG,Lepori; Farma-Lepori, Madrid, Spain or Menopur, Ferring, Madrid, Spain). Initial doses were chosen based on patients’ age and infertility diagnosis. Ovulation induction was monitored by serial ultrasounds and serum estradiol and progesterone levels. Doses were adjusted to the individual patient’s response. Ultrasound-guided egg retrieval was performed 36 h after administration of 250 µg of recombinant human chorionic gonadotropin (hCG; Serono, Madrid, Spain) or 10,000 IU of urinary hCG (Farma-Lepori, Madrid, Spain). In all cases, the fertilization method for the mature oocytes retrieved was intracytoplasmic sperm injection. Embryo transfer was carried out with a Wallace catheter under ultrasound guidance. All retrievals were performed by the same experienced operator.\nMural hGL cells were collected from follicular fluid (FF) obtained during ultrasound-guided transvaginal oocyte retrieval. After removal of the oocyte, FFs from each patient were pooled, and the hGL cells lightly centrifuged. Cells were then washed in “isolation medium” (Medium 199 (Sigma-Aldrich, Missouri, MI, USA), supplemented with sodium bicarbonate (3.7 g/L) (Sigma-Aldrich), penicillin (59 mg/L) (Sigma-Aldrich), streptomycin (100 mg/L) (Sigma-Aldrich), amphotericin B (25 mg/L) (Sigma-Aldrich), L-glutamine (0.29 g/L) (Sigma-Aldrich), and bovine serum albumin (0.1%) (Sigma-Aldrich) and separated from red blood cells using a 50% Percoll (Sigma-Aldrich) gradient. Leukocytes were removed using anti-CD45-coated magnetic beads (Dynabeads M-450 CD45; Dynal ASA, Oslo, Norway) and cellular viability was confirmed by trypan blue exclusion. In all cases, it was greater than 95%.\nTotal RNA from individual patients was extracted using Aurum total RNA mini kit (Bio-Rad Laboratories, California, CA, USA) following the manufacturer’s instructions.\nRNA was reverse transcribed using “iScript cDNA Synthesis kit” (Bio-Rad Laboratories) following the manufacturer’s instructions. Total RNA was reverse transcribed in 20 µL as follows: 25 °C for 5 min and 42 °C for 30 min. The reverse transcriptase was inactivated by heating at 85 °C for 5 min.\nQuantitative reverse transcription polymerase chain reaction of complementary DNA (PCR) was employed to study the relative expression of sirtuin genes in hGL cells. All PCR was carried out using a BioRad CFX96 real-time PCR system (Bio-Rad Laboratories). The specific primers used for each sirtuin gene and the housekeeping β-actin gene used as a reference for mRNA quantification are listed in  Table 3 . The amplification reactions were performed in a 10 µL final volume containing 2× SsoFast EvaGreen Supermix (100 mmol/L KCl, 40 mmol/L Tris- HCl pH 8.4, 0.4 mmol/L of each nucleoside triphosphate, iTaq DNA polymerase 50 U/mL, 6 mmol/L MgCl2, SYBR Green I, 20 nmol/L fluorescein, and stabilizers (Bio-Rad Laboratories) and 0.4 µmol/L of each primer.\nEach sample was analyzed in triplicate, and multiple water blanks were included in the analysis. The thermal profile used for the analysis was as follows: after a 3-min denaturation at 95 °C, 40 cycles of PCR were performed at 95 °C for 5 s and 59 °C for 5 s. Finally, a melting curve program at 65 °C to 95 °C was carried out with a heating rate of 0.1 °C/s and read every 0.5 °C. Expression levels of the genes studied are presented as individual data points as 2 −ΔCT  [ 72 ]. Gene expression values are expressed as x105 relative to β-actin expression.\nStatistical analysis was performed with SPSS 23 software (IBM, New York, NY, USA). Descriptive statistics (mean and standard error (SE) are reported. One-way ANOVA followed by Tukey and Bonferroni post hoc tests were used to carry out comparisons between diagnostic groups. A Spearman rank correlation coefficient was used to assess the relationship between continuous variables. An experiment-wise α of 0.05 was chosen.","source_license":"CC-BY-4.0","license_restricted":false}