The Effect of Sex Differences on Endothelial Function and Circulating Endothelial Progenitor Cells in Hypertriglyceridemia

Ren, Zi; Guo, Jiayi; Xiao, Xingxing; Huang, Jiana; Li, Manchao; Cai, Ruibin; Zeng, Haitao

doi:https://doi.org/10.1155/2020/2132918

Cardiology Research and Practice

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Abstract Introduction Materials and Methods Results and Discussion Discussion Conclusions Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

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Endothelial Injury and Repair in Coronary Heart Disease

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Research Article | Open Access

Volume 2020 | Article ID 2132918 | https://doi.org/10.1155/2020/2132918

The Effect of Sex Differences on Endothelial Function and Circulating Endothelial Progenitor Cells in Hypertriglyceridemia

Zi Ren,¹Jiayi Guo,¹Xingxing Xiao,¹Jiana Huang,¹Manchao Li,¹Ruibin Cai,²and Haitao Zeng¹

Guest Editor: Shiyue Xu

Received14 Feb 2020

Accepted13 Jul 2020

Published21 Sept 2020

Abstract

Background. Men have a higher risk and earlier onset of cardiovascular diseases compared with premenopausal women. Hypertriglyceridemia is an independent risk factor for the occurrence of ischemic heart disease. Endothelial dysfunction is related to the development of ischemic heart disease. Whether sex differences will affect the circulating endothelial progenitor cells (EPCs) and endothelial function in hypertriglyceridemia patients or not is not clear. Methods. Forty premenopausal women and forty age- and body mass index (BMI)-matched men without cardiovascular and metabolic disease were recruited and then divided into four groups: normotriglyceridemic women (women with serum triglycerides level <150 mg/dl), hypertriglyceridemic women (women with serum triglycerides level ≥150 mg/dl), normotriglyceridemic men (men with serum triglycerides level <150 mg/dl), and hypertriglyceridemic men (men with serum triglycerides level ≥150 mg/dl). Peripheral blood was obtained and evaluated. Flow-mediated dilatation (FMD), the number and activity of circulating EPCs, and the levels of nitric oxide (NO), vascular endothelial growth factor (VEGF), and granulocyte-macrophage colony-stimulating factor (GM-CSF) in plasma and culture medium were measured. Results. The number and activity of circulating EPCs, as well as the level of NO in plasma or culture medium, were remarkably increased in premenopausal females compared with those in males both in the hypertriglyceridemic group and the normotriglyceridemic group. The EPC counts and activity, as well as the production of NO, were restored in hypertriglyceridemic premenopausal women compared with those in normal women. However, in hypertriglyceridemic men, the EPC counts and activity, as well as levels of NO, were significantly reduced. The values of VEGF and GM-CSF were without statistical change. Conclusions. The present study firstly demonstrated that there were sex differences in the number and activity of circulating EPCs in hyperglyceridemia patients. Hypertriglyceridemic premenopausal women displayed restored endothelial functions, with elevated NO production, probably mediated by estradiol. We provided a new insight to explore the clinical biomarkers and therapeutic strategies for hypertriglyceridemia-related vascular damage.

1. Introduction

It is well known that atherosclerosis is a progressive inflammatory disease characterized by plaque consisting of cholesterol, fat, calcium, and other substances deposition in the arterial wall. Epidemiological data have suggested that there are remarkably sex differences in the onset of cardiovascular disease (CVD), with atherosclerosis occurring approximately ten years later and myocardial infarction about 20 years later in premenopausal women than in man [1]. However, the risk of CVD rises about ten times in postmenopause women, while only increases 4.6 times in age-matched men [2]. The mechanisms of sex differences in the occurrence of CVD are not fully elucidated. Researches have indicated that estrogen [3] and androgen [4] may play a crucial role in the development of CVD.

Hypertriglyceridemia is commonly defined as fasting triglyceride serum level >150 mg/dl (>1.7 mmol/l) [5]. There is growing evidence suggesting that hypertriglyceridemia is an independent risk factor for ischemic cardiovascular disease [6–11], even slightly elevation of triglycerides was associated with a higher cardiovascular risk [8] and mortality rate [9]. In the general population, compared with the individuals with nonfasting triglycerides of 70 mg/dL (0.8 mmol/L), individuals with levels of 580 mg/dL (6.6 mmol/L) have sharply increased risks of myocardial infarction for 5.1-fold, ischemic heart disease, and ischemic stroke for 3.2-fold, respectively, and all-cause mortality for 2.2-fold [11]. Lipid-lowering treatment with statins was proved to exert a positive effect on patients with atherosclerosis through restoring the endothelial function and increased circulating endothelial progenitor cells (EPCs) [12, 13]. However, some researches have indicated patients with atherosclerosis may not get enough protection by statins alone [14], especially in patients with systemic inflammation [15]. Besides, statins may have some side effects such as statin-associated symptoms (SAS), including muscle or central nervous system symptoms and diabetes [16].

Vascular endothelium cell, nature’s blood container, is the dynamic regulator of hemostasis and thrombosis with the function of recruitment and activation of platelet and coagulation cascade [17]. Therefore, vascular endothelium dysfunction was proven to be a significant risk factor for vascular diseases, such as atherosclerosis [18] and insulin resistance [19, 20]. Asahara et al. have firstly described that EPCs isolated from peripheral blood play a crucial role in angiogenesis [21]. Early EPCs, derivatives of CD14+ monocytic cell lineage [22], promote angiogenesis by secreting inflammatory cytokines and paracrine angiogenic factors [23]. While late EPCs, originating from CD34+ hematopoietic stem cells [24, 25], are associated with endothelial tubulogenesis and neovascularization via enhanced expression of proliferation and angiogenesis genes [23]. EPCs promote angiogenesis or vascular repair through activation of resident endothelial cells and recruitment of endogenous monocytes/macrophages to sites of ischemia, which were mediated by paracrine factors [26] such as vascular endothelial growth factor (VEGF) [27–29], granulocyte-macrophage colony-stimulating factor (GM-CSF) [29–32], and nitric oxide (NO) [32–34]. Dyslipidemia, hyperglycemia, insulin resistance, and induced EPC dysfunction via disrupting the SDF-1/CXCR-4 and NO pathways and the p53/SIRT1/p66Shc axis are critical for mobilization, migration, homing, and vasculogenic properties [35]. Researches also have indicated that EPC therapy is a safe and efficient way to delay the progression of atherosclerosis [36] and improve the heart function [37] for patients with coronary heart disease.

Our previous study has demonstrated that premenopausal women in prehypertension status present an increased circulating EPC number and elevated NO level, which may associate with the vascular protection effect of premenopausal women [38]. In this study, we will further investigate the sex differences of the endothelial function and circulating EPCs in patients of hypertriglyceridemia, and the probable underlying mechanisms.

2. Materials and Methods

The materials and methods section should contain sufficient detail so that all procedures can be repeated. It may be divided into headed subsections if several methods are described.

2.1. Characteristics of Subjects

Forty premenopausal women and forty age- and BMI-matched men without cardiovascular and metabolic disease were recruited. Based on the Adult Treatment Panel III (ATP-III) guidelines [5], according to the triglyceride level and sex, we divided the subjects into four groups: normotriglyceridemic women (women with serum triglycerides level <150 mg/dl), high triglyceridemic (HTG) women (women with serum triglycerides level ≥150 mg/dl), normotriglyceridemic men (men with serum triglycerides level <150 mg/dl), HTG men (men with serum triglycerides level ≥150 mg/dl). Patients with diabetes, tumor or cancer, and infection or inflammatory disease were excluded. Besides, we also excluded the smokers, alcohol abusers, pregnant, women undergoing breastfeeding, or patients with a history of hysterectomy, oophorectomy, or irregular menstrual cycles. All the subjects were given informed consent, and the experimental protocols were approved by the ethics committee of our hospital. The characteristics of the subjects are listed in Table 1.

2.2. Blood Samples

The peripheral blood was obtained from the patients in the early morning after overnight fasting. Caffeinated beverage or alcohol was forbidden for at least 12 hours before blood draw. None of the patients were taking any medicines such as statins, antiplatelet, or anti-inflammatory that may have an impact on the parameters of EPCs. The following items were detected and evaluated: AST (aspartate aminotransferase), ALT (alanine aminotransferase), BUN (blood urea nitrogen), Cr (creatinine), LDL (low-density lipoprotein), TC (total cholesterol), HDL (high-density lipoprotein), TG (triglyceride), FPG (fasting plasma glucose), estradiol, and so on, which are presented in Table 1.

2.3. Evaluation of the EPC Number and Activity

The number of circulating EPCs was evaluated by flow cytometry analysis and cell culture assay, and EPC activity was measured by EPC migration and proliferation assay, which were demonstrated in our previous studies [38, 39].

2.4. Measurement of the Plasma Levels of NO, VEGF, and GM-CSF and Secretion by EPCs

The plasma levels of NO, VEGF, and GM-CSF and secretion by cultured EPCs were evaluated by methods as we described previously [38, 39].

2.5. Measurement of FMD

Flow-mediated dilation (FMD) of the brachial artery was used to evaluate the endothelial function. The detailed method was demonstrated in our previous studies [40, 41].

2.6. Statistical Analysis

SPSS Version 26.0 statistical software (SPSS Inc., Chicago, Illinois) was used for data analysis. Results were expressed as mean value ± standard deviation. Two-factor ANOVA was used for comparisons between the four groups (sex and the status of normal triglyceridemia or hypertriglyceridemia). When there was a significant F value, a post hoc test was then performed with the Newman–Keuls method to identify significant differences among mean values. Univariate correlations were analyzed by Pearson’s coefficient (r). was considered as statistically significant.

3. Results and Discussion

3.1. Baseline Clinical Characteristics

As we have shown in Table 1, there were no significant differences in age, BMI, and serum TG, TC, LDL, and HDL among the four groups (). The serum TG levels of both premenopausal HTG women () and HTG men () were remarkably increased than those in the normotriglyceridemic groups. The serum level of estradiol and the value of FMD were higher in the female groups than in the male groups (both normotriglyceridemic and HCG groups, and , respectively). Moreover, FMD was obviously lower in the HMG men compared with that in the normotriglyceridemic men (). However, the value of FMD in normotriglyceridemic women and HMG women did not have remarkable differences ().

3.2. EPC Number and Activity in the Four Groups

The number of EPCs evaluated by FACS analysis and cell culture assay of four groups is shown in Figure 1. The number of EPCs in the normotriglyceridemic groups was close to that in the hypertriglyceridemic groups of the same sex, both men and women ( and , respectively) (Figures 1(a) and 1(b)). However, the number of EPCs in men, both normotriglyceridemic and hypertriglyceridemic groups, was drastically lower than that in women () (Figures 1(a) and 1(b)).

(a)

(b)

The migratory and the proliferative activities of EPCs were significantly higher in both normotriglyceridemic and hypertriglyceridemic premenopausal female groups than those in the male groups ( and , respectively) (Figures 2(a) and 2(b)). Besides, in the male groups, the migratory and the proliferative activities of EPCs were statistically decreased in the hypertriglyceridemic men compared with those in the normotriglyceridemic men () (Figures 2(a) and 2(b)). However, the activity of EPCs in normotriglyceridemic premenopausal women was not remarkably different from that in hypertriglyceridemic premenopausal women () (Figures 2(a) and 2(b)).

(a)

(b)

Figure 2

(a) The migratory and (b) the proliferative activities of EPCs were statically elevated in the female groups (both normotriglyceridemic and hypertriglyceridemic) than those in the male groups. The migratory and the proliferative activities of EPCs were lower in the hypertriglyceridemic men group than those in the normotriglyceridemic men group. However, the migratory and the proliferative activities of EPCs in normotriglyceridemic premenopausal women were similar to those in hypertriglyceridemic premenopausal women. Data were presented as mean and standard deviation. ☆vs. normotriglyceridemic. #vs premenopausal women.

3.3. Levels of NO, VEGF, and GM-CSF in Plasma or Culture Media in the Four Groups

The level of NO from plasma or culture media of the normotriglyceridemic and hypertriglyceridemic men groups was remarkably lower than that of the premenopausal women groups ( and , respectively) (Figures 3(a) and 4(a)). However, the differences in plasma level of NO or the level of NO secreted by cultured EPCs between the normotriglyceridemic and hypertriglyceridemic premenopausal female groups did not reach statistical significance ( and , respectively) (Figures 3(a) and 4(a)). In addition, the level of NO in plasma or cultured media of the hypertriglyceridemic men was statistically elevated compared with that from the normotriglyceridemic men ( and , respectively) (Figures 3(a) and 4(a)). Nevertheless, there were no drastic differences in VEGF or GM-CSF plasma level or secretion between four groups (Figures 3(b), 3(c), 4(b), and 4(c)).

(a)

(b)

(c)

Figure 3

The plasma levels of NO, VEGF, and GM-CSF. (a) The plasma levels of NO in normotriglyceridemic and hypertriglyceridemic men were statically lower than those in the female groups (). In the male groups, the level of NO was decreased in hypertriglyceridemic subjects than that in normotriglyceridemic subjects (). The plasma levels of NO between normotriglyceridemic and hypertriglyceridemic premenopausal female groups displayed no significant difference (). (b) and (c) The plasma level of VEGF and GM-CSF had no statistical difference between the four groups.

(a)

(b)

(c)

Figure 4

The levels of NO, VEGF, and GM-CSF secreted by cultured EPCs. (a) The level of NO produced by cultured EPCs of the normotriglyceridemic and hypertriglyceridemic men groups was remarkably lower than that of the premenopausal women groups. Besides, the secretion of NO from hypertriglyceridemic men was statically elevated compared with that from normotriglyceridemic men. Nevertheless, the level of NO in the EPCs cultural media of the hypertriglyceridemic premenopausal women was not significantly different from that of the normotriglyceridemic premenopausal women). (b) and (c) There was no obvious difference in VEGF or GM-CSF secretion between four groups.

3.4. Correlation between FMD and EPCs or NO Level

FMD, which reflected the endothelial function, was positively relevant with the migratory (r = 0.57, ) and the proliferative (r = 0.46, ) activity of circulating ECPs (Figures 5(a) and 5(b)). Moreover, there was a positive correlation between FMD and the plasma NO level (r = 0.62, ) or level of NO secreted by cultured EPCs (r = 0.44, ) (Figures 5(c) and 5(d)).

(a)

(b)

(c)

(d)

4. Discussion

Our research firstly demonstrated sex effects on the endothelial function and circulating endothelial progenitor cells in hypertriglyceridemic patients, which may be probably attributed to the disturbance of NO production. We have evaluated that the number and activity of EPCs were preserved in premenopausal women compared with those in the age-matched men in hypertriglyceridemic status. Besides, the plasma level of NO or NO level secreted by EPCs in the culture media was higher in the premenopausal hypertriglyceridemic women than in men. Moreover, there was a positive correlation between EPCs activity or the NO level and endothelial functions evaluated by FMD.

It is well documented that there are sex differences in the occurrence of ischemic heart disease. Generally, males tend to have earlier onset [1] of occlusive coronary artery disease (CAD) [42] with more severe infarction foci and poor recovery [43–45] than females. EPCs are essential for the intrinsic repair and regeneration process of the injured myocardium [46]. Ischemic heart disease was proved to be associated with depletion of circulating EPCs [47, 48] and higher local density of EPCs [48]. Coincidently, in comparison with men or postmenopausal women, premenopausal women exhibit a higher level of circulating EPCs with better colony-forming capacity and migratory activity [49–52]. This phenomenon was consistent with that of the previous studies of the sex differences in the occurrence of ischemic heart disease, which implied that the better cardiovascular repaired and protective capacity in premenopausal women might partly attribute to the enhanced number and activity of EPCs. Hypertriglyceridemia is proved to be an independent risk factor of cardiovascular disease [6–11]. However, there were no scientific data revealing the relationship between sex differences and hypertriglyceridemia and EPCs. Hence, we postulated that the sex differences in circulating EPCs might also exist in hypertriglyceridemia.

We have studied the number and activity differences in circulating EPCs among four groups. Generally, the number of circulating EPCs in male groups (both the hypertriglyceridemia and the control) was higher than that in the age-matched premenopausal female groups, while the activity of EPCs was depleted compared with that of female groups, which were consistent with the previous studies [49–52]. Furthermore, we noticed that, in the male groups, the number and activity of EPCs are drastically reduced in patients with hypertriglyceridemia, which suggested the depletion of the number and activity of EPCs in hypertriglyceridemia may at least partly explain the higher risk of ischemic heart disease in hypertriglyceridemic male patients. Interestingly, we found that the number and activity of circulating EPCs in hypertriglyceridemic premenopausal women was nearly identical to that in normotriglyceridemic premenopausal women. The present results suggested the restoration of endogenous vascular endothelial repair capacity in premenopausal women, even in hypertriglyceridemia status. The reduction of number and activity of EPCs only existed in hypertriglyceridemic males rather than in the hypertriglyceridemic premenopausal female, indicating that a higher tendency of ischemic heart disease in hypertriglyceridemic men than in hypertriglyceridemic premenopausal women may be due to the sex differences in endogenous endothelial repair capacity.

It is well known that EPCs promoting angiogenesis or vascular repair is mediated by paracrine molecules such as VEGF [27–29], GM-CSF [29–32], and NO [32–34]. Previous studies elucidated that elevation of triglycerides was inversely correlated with the level of NO [53–55]. Therefore, we hypothesized that the sex differences in EPCs in patients with hypertriglyceridemia might be related to the alteration of the production of VEGF, GM-CSF, or NO. We detected the plasma level of NO, VEGF, and GM-CSF in the four groups. Similar to the sex differences in the changes of circulating EPCs in hypertriglyceridemia status, we found that the NO plasma level was lower in male groups than in premenopausal female groups, which was consistent with those of the previous studies in healthy subjects [56]. Besides, the plasma NO level was restored in premenopausal women in hypertriglyceridemia status compared with that in women in the control group. In our previous research, we have elucidated the positive correlation between plasma NO level and the number or activity of circulating EPCs [38]. Therefore, it suggested that the restoration of number and activity of circulating EPCs in hypertriglyceridemic premenopausal women may be attributed to the stability of exogenous NO production. Nevertheless, we did not observe a significant change in the plasma level of VEGF or GM-CSF among four groups, implicating that VEGF and GM-CSF may not be the key factors contributing to the sex differences in hypertriglyceridemia.

NO was generated by endothelial nitric oxide synthase (eNOS), which acts as a key regulator for the homeostasis of endothelial function [57]. Therefore, we further investigated the sex differences in NO production by EPCs. And, we found that the level of NO secreted by EPCs was similar to the change of the NO plasma level. As we have mentioned before, NO secretion by EPCs is significantly correlated with the number and activity of circulating EPCs [38]. Our result suggested that enhanced endogenous NO production would probably help to preserve the number and activity of circulating EPCs in hypertriglyceridemic women. In addition, there was no remarkable difference in the production of VEGF and GM-CSF, which further suggested that VEGF and GM-CSF did not participate in the sex differences in the EPCs of hypertriglyceridemia.

FMD is an indicator of endothelial function. We further investigated the relationship between FMD and EPCs or NO. The result revealed that the activity of EPCs and NO exogenous or endogenous production was positively correlated with the endothelial function.

In general, we discovered the conservation of endothelial function with EPC counts and activity in hypertriglyceridemic premenopausal women, which may be attributed to the enhanced production of NO. It is well documented that NO plays an essential role in the maintenance of vascular homeostasis, including regulation of vascular dilator tone, modulation of local cell growth, and protection of vessels [58]. Endothelial cells, as well as vascular smooth muscle cells, are crucial targets of estradiol [59]. Furthermore, estradiol activates early and late endothelial eNOS via binding the estrogen receptors through nongenomic and genomic pathways [60]. Undoubtedly, the remarkable difference between premenopausal women and age-matched men is the estradiol level. Hence, we inferred that estradiol augmented NO production and thereby increased the number and activity of circulating EPCs in hypertriglyceridemia.

The present study demonstrated a new insight into the evaluation and therapeutic targets of hypertriglyceridemia-related endothelium injury. Firstly, we showed the sex differences in circulating EPC counts and activity, indicating that EPCs and FMD could act as an essential clinical biomarker to detect hypertriglyceridemia-related vascular injury. Secondly, the correlation of higher cardiovascular risk with the reduction of EPC counts and activity in men compared with that in premenopausal women reminded us that enhancement of circulating EPC counts and activity is a potential therapeutic target to reverse the hypertriglyceridemia-related endothelial damage. Furthermore, our study also revealed that enhanced NO production was essential for the improvement of EPC number and activity. Hence, we advocated that patients with hypertriglyceridemia could adopt some strategies, such as exercises [39, 61], to stimulate NO production and thereby improve the endothelial repair capacity.

5. Conclusions

The present study raised a new view that there were sex differences in the number and activity of circulating EPCs in hyperglyceridemia patients. Hypertriglyceridemic premenopausal women displayed restored endothelial functions, which was associated with the enhanced NO production, probably mediated by estradiol. We provided a new insight to explore the clinical biomarkers and therapeutic strategies for hypertriglyceridemia-related vascular damage.

Data Availability

The datasets used in the current study can be made available from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare no conflicts of interest.

Authors’ Contributions

Zi Ren, Jiayi Guo, and Xingxing Xiao these authors contributed equally to this work.

Acknowledgments

The study was financially supported by the grants from the National Natural Scientific Foundation of China (81670220, 31270992, and 30800215), the Project of Guangdong Province Science and Technology Plan (2015A020212013 and 2013B021800275), Guangdong Natural Science Foundation (2014A030313086), the Fundamental Research Funds for the Central Universities in Sun Yat-sen University (17ykzd18 and 13ykpy24), and the Project of Zhu Jiang Science and Technology New Star of Guangzhou City (2013J2200019).

References

P. Mathur, B. Ostadal, F. Romeo, and J. L. Mehta, “Gender-related differences in atherosclerosis,” Cardiovascular Drugs and Therapy, vol. 29, no. 4, pp. 319–327, 2015.
View at: Publisher Site | Google Scholar
W. L. Duvall, “Cardiovascular disease in women,” Mount Sinai Journal of Medicine, vol. 70, no. 5, pp. 293–305, 2003.
View at: Google Scholar
L. R. Pedersen, D. Frestad, M. M. Michelsen et al., “Risk factors for myocardial infarction in women and men: a review of the current literature,” Current Pharmaceutical Design, vol. 22, no. 25, pp. 3835–3852, 2016.
View at: Publisher Site | Google Scholar
S. Chaudhari, S. C. Cushen, O. Osikoya et al., “Mechanisms of sex disparities in cardiovascular function and remodeling,” Comprehensive Physiology, vol. 9, no. 1, pp. 375–411, 2018.
View at: Publisher Site | Google Scholar
Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults, “Executive summary of the third report of the national cholesterol education program (ncep) expert Panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult treatment Panel iii),” JAMA: The Journal of the American Medical Association, vol. 285, no. 19, pp. 2486–2497, 2001.
View at: Publisher Site | Google Scholar
I. Holme and S. Tonstad, “Association of coronary heart disease mortality with risk factors according to length of follow-up and serum cholesterol level in men: the oslo study cohort,” European Journal of Preventive Cardiology, vol. 20, no. 1, pp. 168–175, 2013.
View at: Publisher Site | Google Scholar
S. Bansal, J. E. Buring, N. Rifai, S. Mora, F. M. Sacks, and P. M. Ridker, “Fasting compared with nonfasting triglycerides and risk of cardiovascular events in women,” JAMA, vol. 298, no. 3, pp. 309–316, 2007.
View at: Publisher Site | Google Scholar
O. Faergeman, I. Holme, R. Fayyad et al., “Plasma triglycerides and cardiovascular events in the treating to new targets and incremental decrease in end-points through aggressive lipid lowering trials of statins in patients with coronary artery disease,” The American Journal of Cardiology, vol. 104, no. 4, pp. 459–463, 2009.
View at: Publisher Site | Google Scholar
R. Klempfner, A. Erez, B.-Z. Sagit et al., “Elevated triglyceride level is independently associated with increased all-cause mortality in patients with established coronary heart disease,” Circulation: Cardiovascular Quality and Outcomes, vol. 9, no. 2, pp. 100–108, 2016.
View at: Publisher Site | Google Scholar
H. Iso, H. Imano, K. Yamagishi et al., “Fasting and non-fasting triglycerides and risk of ischemic cardiovascular disease in Japanese men and women: the circulatory risk in communities study (circs),” Atherosclerosis, vol. 237, no. 1, pp. 361–368, 2014.
View at: Publisher Site | Google Scholar
B. G. Nordestgaard, “Triglyceride-rich lipoproteins and atherosclerotic cardiovascular disease,” Circulation Research, vol. 118, no. 4, pp. 547–563, 2016.
View at: Publisher Site | Google Scholar
E. Oikonomou, G. Siasos, M. Zaromitidou et al., “Atorvastatin treatment improves endothelial function through endothelial progenitor cells mobilization in ischemic heart failure patients,” Atherosclerosis, vol. 238, no. 2, pp. 159–164, 2015.
View at: Publisher Site | Google Scholar
M. Vasa, S. Fichtlscherer, K. Adler et al., “Increase in circulating endothelial progenitor cells by statin therapy in patients with stable coronary artery disease,” Circulation, vol. 103, no. 24, pp. 2885–2890, 2001.
View at: Publisher Site | Google Scholar
J. Nilsson, “Atherosclerotic plaque vulnerability in the statin era,” European Heart Journal, vol. 38, no. 21, pp. 1638–1644, 2017.
View at: Publisher Site | Google Scholar
A. O. Spiel, F. B. Mayr, J. M. Leitner, C. Firbas, W. Sieghart, and B. Jilma, “Simvastatin and rosuvastatin mobilize endothelial progenitor cells but do not prevent their acute decrease during systemic inflammation,” Thrombosis Research, vol. 123, no. 1, pp. 108–113, 2008.
View at: Publisher Site | Google Scholar
P. D. Thompson, G. Panza, A. Zaleski, and B. Taylor, “Statin-associated side effects,” Journal of the American College of Cardiology, vol. 67, no. 20, pp. 2395–2410, 2016.
View at: Publisher Site | Google Scholar
H. Kwaan and M. Samama, “The significance of endothelial heterogeneity in thrombosis and hemostasis,” Seminars in Thrombosis and Hemostasis, vol. 36, no. 3, pp. 286–300, 2010.
View at: Publisher Site | Google Scholar
M. A. Gimbrone Jr. and G. García-Cardeña, “Vascular endothelium, hemodynamics, and the pathobiology of atherosclerosis,” Cardiovascular Pathology, vol. 22, no. 1, pp. 9–15, 2013.
View at: Publisher Site | Google Scholar
D. Prieto, C. Contreras, and A. Sánchez, “Endothelial dysfunction, obesity and insulin resistance,” Current Vascular Pharmacology, vol. 12, no. 3, pp. 412–426, 2014.
View at: Publisher Site | Google Scholar
S. Del Turco, M. Gaggini, G. Daniele et al., “Insulin resistance and endothelial dysfunction: a mutual relationship in cardiometabolic risk,” Current Pharmaceutical Design, vol. 19, no. 13, pp. 2420–2431, 2013.
View at: Publisher Site | Google Scholar
T. Asahara, T. Murohara, A. Sullivan et al., “Isolation of putative progenitor endothelial cells for angiogenesis,” Science, vol. 275, no. 5302, pp. 964–966, 1997.
View at: Publisher Site | Google Scholar
G. Krenning, B. W. A. van der Strate, M. Schipper et al., “CD34+ cells augment endothelial cell differentiation of CD14+endothelial progenitor cellsin vitro,” Journal of Cellular and Molecular Medicine, vol. 13, no. 8, pp. 2521–2533, 2009.
View at: Publisher Site | Google Scholar
C.-C. Cheng, S.-J. Chang, Y.-N. Chueh et al., “Distinct angiogenesis roles and surface markers of early and late endothelial progenitor cells revealed by functional group Analyses,” BMC Genomics, vol. 14, no. 1, p. 182, 2013.
View at: Publisher Site | Google Scholar
M. C. Yoder, L. E. Mead, D. Prater et al., “Redefining endothelial progenitor cells via clonal analysis and hematopoietic stem/progenitor cell principals,” Blood, vol. 109, no. 5, pp. 1801–1809, 2007.
View at: Publisher Site | Google Scholar
D. Rana, A. Kumar, and S. Sharma, “Endothelial progenitor cells as molecular targets in vascular senescence and repair,” Current Stem Cell Research & Therapy, vol. 13, no. 6, pp. 438–446, 2018.
View at: Publisher Site | Google Scholar
J. Rehman, J. Li, C. M. Orschell, and K. L. March, “Peripheral blood “endothelial progenitor cells” are derived from monocyte/macrophages and secrete angiogenic growth factors,” Circulation, vol. 107, no. 8, pp. 1164–1169, 2003.
View at: Publisher Site | Google Scholar
L. Li, H. Liu, C. Xu et al., “VEGF promotes endothelial progenitor cell differentiation and vascular repair through connexin 43,” Stem Cell Research & Therapy, vol. 8, no. 1, p. 237, 2017.
View at: Publisher Site | Google Scholar
S. Aday, J. Zoldan, M. Besnier et al., “Synthetic microparticles conjugated with VEGF165 improve the survival of endothelial progenitor cells via microrna-17 inhibition,” Nature Communications, vol. 8, no. 1, p. 747, 2017.
View at: Publisher Site | Google Scholar
T. M. Powell, J. D. Paul, J. M. Hill et al., “Granulocyte colony-stimulating factor mobilizes functional endothelial progenitor cells in patients with coronary artery disease,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 25, no. 2, pp. 296–301, 2005.
View at: Publisher Site | Google Scholar
C. Qiu, Q. Xie, D. Zhang et al., “GM-CSF induces cyclin D1 expression and proliferation of endothelial progenitor cells via Pi3k and mapk signaling,” Cellular Physiology and Biochemistry, vol. 33, no. 3, pp. 784–795, 2014.
View at: Publisher Site | Google Scholar
S. Bruno, B. Bussolati, P. Scacciatella et al., “Combined administration of G-csf and gm-csf stimulates monocyte-derived pro-angiogenic cells in patients with acute myocardial infarction,” Cytokine, vol. 34, no. 1-2, pp. 56–65, 2006.
View at: Publisher Site | Google Scholar
J. Schuett, H. Schuett, R. Oberoi et al., “NADPH oxidase NOX2 mediates TLR2/6-dependent release of GM-CSF from endothelial cells,” The FASEB Journal, vol. 31, no. 6, pp. 2612–2624, 2017.
View at: Publisher Site | Google Scholar
Z. S. Katusic and S. A. Austin, “Endothelial nitric oxide: protector of a healthy mind,” European Heart Journal, vol. 35, no. 14, pp. 888–894, 2014.
View at: Publisher Site | Google Scholar
F. Bonafè, C. Guarnieri, and C. Muscari, “Nitric oxide regulates multiple functions and fate of Adult progenitor and stem cells,” Journal of Physiology and Biochemistry, vol. 71, no. 1, pp. 141–153, 2015.
View at: Publisher Site | Google Scholar
J. Wils, J. Favre, and J. Bellien, “Modulating putative endothelial progenitor cells for the treatment of endothelial dysfunction and cardiovascular complications in diabetes,” Pharmacology & Therapeutics, vol. 170, pp. 98–115, 2017.
View at: Publisher Site | Google Scholar
A. Georgescu, N. Alexandru, E. Andrei, E. Dragan, D. Cochior, and S. Dias, “Effects of transplanted circulating endothelial progenitor cells and platelet microparticles in atherosclerosis development,” Biology of the Cell, vol. 108, no. 8, pp. 219–243, 2016.
View at: Publisher Site | Google Scholar
F.-Y. Lee, Y.-L. Chen, P.-H. Sung et al., “Intracoronary transfusion of circulation-derived CD34+ cells improves left ventricular function in patients with end-stage diffuse coronary artery disease unsuitable for coronary intervention∗,” Critical Care Medicine, vol. 43, no. 10, pp. 2117–2132, 2015.
View at: Publisher Site | Google Scholar
Y. Zhen, S. Xiao, Z. Ren et al., “Increased endothelial progenitor cells and nitric oxide in young prehypertensive women,” The Journal of Clinical Hypertension, vol. 17, no. 4, pp. 298–305, 2015.
View at: Publisher Site | Google Scholar
Z. Yang, J.-M. Wang, L. Chen, C.-F. Luo, A.-L. Tang, and J. Tao, “Acute exercise-induced nitric oxide production contributes to upregulation of circulating endothelial progenitor cells in healthy subjects,” Journal of Human Hypertension, vol. 21, no. 6, pp. 452–460, 2007.
View at: Publisher Site | Google Scholar
H. Zeng, Y. Jiang, H. Tang et al., “Abnormal phosphorylation of tie2/akt/enos signaling pathway and decreased number or function of circulating endothelial progenitor cells in prehypertensive premenopausal women with diabetes mellitus,” BMC Endocrine Disorders, vol. 16, no. 1, p. 13, 2016.
View at: Publisher Site | Google Scholar
J. Liu, D. J. Hu, H. Yan et al., “Attenuated endothelial function is associated with decreased endothelial progenitor cells and nitric oxide in premenopausal diabetic women,” Molecular Medicine Reports, vol. 18, no. 5, pp. 4666–4674, 2018.
View at: Publisher Site | Google Scholar
V. Regitz-Zagrosek and G. Kararigas, “Mechanistic pathways of sex differences in cardiovascular disease,” Physiological Reviews, vol. 97, no. 1, pp. 1–37, 2017.
View at: Publisher Site | Google Scholar
R. Puglisi, G. Mattia, A. Carè et al., “Non-genomic effects of estrogen on cell homeostasis and remodeling with special focus on cardiac ischemia/reperfusion injury,” Frontiers in Endocrinology, vol. 10, p. 733, 2019.
View at: Publisher Site | Google Scholar
S. Menazza, J. Sun, S. Appachi et al., “Non-nuclear estrogen receptor alpha activation in endothelium reduces cardiac ischemia-reperfusion injury in mice,” Journal of Molecular and Cellular Cardiology, vol. 107, pp. 41–51, 2017.
View at: Publisher Site | Google Scholar
J. A. Fels and G. Manfredi, “Sex differences in ischemia/reperfusion injury: the role of mitochondrial permeability transition,” Neurochemical Research, vol. 44, no. 10, pp. 2336–2345, 2019.
View at: Publisher Site | Google Scholar
M. W. Morris Jr. and K. W. Liechty, “Cardiac progenitor cells in myocardial infarction wound healing: a critical review,” Advances in Wound Care, vol. 2, no. 6, pp. 317–326, 2013.
View at: Publisher Site | Google Scholar
A. E. Berezin and A. A. Kremzer, “Circulating endothelial progenitor cells as markers for severity of ischemic chronic heart failure,” Journal of Cardiac Failure, vol. 20, no. 6, pp. 438–447, 2014.
View at: Publisher Site | Google Scholar
D. Morrone, F. Felice, C. Scatena et al., “Role of circulating endothelial progenitor cells in the reparative mechanisms of stable ischemic myocardium,” International Journal of Cardiology, vol. 257, pp. 243–246, 2018.
View at: Publisher Site | Google Scholar
G. L. Hoetzer, O. J. MacEneaney, H. M. Irmiger et al., “Gender differences in circulating endothelial progenitor cell colony-forming capacity and migratory activity in middle-aged adults,” The American Journal of Cardiology, vol. 99, no. 1, pp. 46–48, 2007.
View at: Publisher Site | Google Scholar
A. Rousseau, F. Ayoubi, C. Deveaux et al., “Impact of age and gender interaction on circulating endothelial progenitor cells in healthy subjects,” Fertility and Sterility, vol. 93, no. 3, pp. 843–846, 2010.
View at: Publisher Site | Google Scholar
G. P. Fadini, S. de Kreutzenberg, M. Albiero et al., “Gender differences in endothelial progenitor cells and cardiovascular risk profile,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 28, no. 5, pp. 997–1004, 2008.
View at: Publisher Site | Google Scholar
M. L. Topel, S. S. Hayek, Y. A. Ko et al., “Sex differences in circulating progenitor cells,” Journal of the American Heart Association, vol. 6, no. 10, 2017.
View at: Publisher Site | Google Scholar
C. M. Volpe, L. F. Abreu, P. S. Gomes et al., “The production of nitric oxide, IL-6, and TNF-alpha in palmitate-stimulated pbmncs is enhanced through hyperglycemia in diabetes,” Oxidative Medicine and Cellular Longevity, vol. 2014, Article ID 479587, 12 pages, 2014.
View at: Publisher Site | Google Scholar
P. Chedraui, G. S. Escobar, C. Ramírez et al., “Nitric oxide and pro-inflammatory cytokine serum levels in postmenopausal women with the metabolic syndrome,” Gynecological Endocrinology, vol. 28, no. 10, pp. 787–791, 2012.
View at: Publisher Site | Google Scholar
A. Vignini, L. Nanetti, C. Moroni et al., “Platelet nitric oxide production and Ir: relation with obesity and hypertriglyceridemia,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 18, no. 8, pp. 553–558, 2008.
View at: Publisher Site | Google Scholar
P. Forte, B. J. Kneale, E. Milne et al., “Evidence for a difference in nitric oxide biosynthesis between healthy women and men,” Hypertension, vol. 32, no. 4, pp. 730–734, 1998.
View at: Publisher Site | Google Scholar
M. Siragusa and I. Fleming, “The enos signalosome and its link to endothelial dysfunction,” Pflügers Archiv-European Journal of Physiology, vol. 468, no. 7, pp. 1125–1137, 2016.
View at: Publisher Site | Google Scholar
D. Tousoulis, A.-M. Kampoli, C. Tentolouris Nikolaos Papageorgiou, and C. Stefanadis, “The role of nitric oxide on endothelial function,” Current Vascular Pharmacology, vol. 10, no. 1, pp. 4–18, 2012.
View at: Publisher Site | Google Scholar
A. A. Knowlton and A. R. Lee, “Estrogen and the cardiovascular system,” Pharmacology & Therapeutics, vol. 135, no. 1, pp. 54–70, 2012.
View at: Publisher Site | Google Scholar
K. E. Kypreos, S. Zafirovic, P.-I. Petropoulou et al., “Regulation of endothelial nitric oxide synthase and high-density lipoprotein quality by estradiol in cardiovascular pathology,” Journal of Cardiovascular Pharmacology and Therapeutics, vol. 19, no. 3, pp. 256–268, 2014.
View at: Publisher Site | Google Scholar
A. S. Zago, L. Reis Silveira, E. Kokubun et al., “Effects of aerobic exercise on the blood pressure, oxidative stress and enos gene polymorphism in pre-hypertensive older people,” European Journal of Applied Physiology, vol. 110, no. 4, pp. 825–832, 2010.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Zi Ren et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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