- Original article
- Open Access
Association between high-density lipoprotein-cholesterol and hypertension in relation to circulating CD34-positive cell levels
Journal of Physiological Anthropology volume 36, Article number: 26 (2017)
Although high-density lipoprotein-cholesterol (HDL) level is inversely correlated with cardiovascular events, HDL is also reported to be positively associated with hypertension, which is a known endothelial impairment factor. Since HDL mediates important protective actions on the vascular endothelium by increasing the number of circulating endothelial progenitor cells (CD34-positive cells), the level of circulating CD34-positive cells should influence the association between HDL and hypertension.
To investigate the association between HDL and hypertension in relation to the level of circulating CD34-positive cells, we conducted a cross-sectional study of 477 elderly men aged 60–69 years who participated in general health checkup.
HDL was found to be significantly positively associated with hypertension in subjects with a high level of circulating CD34-positive cells, while no significant association was observed for subjects with low circulating CD34-positive cells. Known cardiovascular risk factors adjusted odds (ORs) and 95% confidence intervals (CIs) of hypertension for increments of one standard deviation (SD) in HDL (13.8 mg/dL) were 1.44 (1.06, 1.96) for subjects with a high level of circulating CD34-positive cells and 0.87 (0.63, 1.19) for subjects with low circulating CD34-positive cells. We also revealed a significant association between HDL level and CD34-positive cell level on hypertension, with fully adjusted p values for the effect of this interaction on hypertension at 0.022.
Independent of known cardiovascular risk factors, HDL was found to be positively associated with hypertension in subjects with a high level of circulating CD34-positive cells but not for subjects with low circulating CD34-positive cells.
A previous Japanese study reported hypertension as an important risk factor for coronary disease . Additionally, low levels of high-density lipoprotein-cholesterol (HDL) are associated with increased risk of coronary artery disease . These studies led us to speculate that low levels of HDL are associated with a higher prevalence of hypertension. However, a previous Japanese cross-sectional study reported that HDL is independently positively associated with hypertension in apparently healthy Japanese men and women .
Recently, numerous studies have reported a bidirectional association between hypertension and endothelial dysfunction—hypertension induces increased arterial stiffness and vice versa [4,5,6,7,8,9,10]. The cycle between hypertension and endothelial dysfunction has been established, and the process of endothelial repair should also play an important role with regard to breaking away from this vicious cycle.
On the other hand, bone marrow-derived endothelial progenitor cells such as CD34-positive cells have been reported to contribute to endothelial repair [11,12,13], and circulating CD34-positive cells contribute to the maintenance of cerebral circulation in an ischemic stress setting. A strong inverse correlation between the number of circulating CD34-positive cells and cerebral infarction has been shown . Another study reported an inverse correlation between the level of cognitive impairment and the number of circulating CD34-positive cells in patients with vascular-type cognitive impairment . Therefore, subjects with a high level of CD34-positive cells should have elevated endothelial repair activity [6, 16,17,18]. Since endothelial repair activity should be stimulated by endothelial injury, subjects with a high level of CD34-positive cells should present with endothelial injury similar to participants with stable cardiovascular disease and acute coronary syndrome. In addition to the above, unlike HDL from healthy subjects, HDL from participants with stable cardiovascular disease or acute coronary syndrome is reported to be lacking in endothelial anti-inflammatory effects and does not stimulate endothelial repair .
Given the above, we hypothesized that the positive association between HDL and hypertension occurs only in subjects with a high level of circulating CD34-positive cells.
To investigate this association, we conducted a cross-sectional study of 477 elderly men aged 60–69 years who participated in an annual health checkup from 2013 to 2015.
Materials and methods
This study was approved by the Ethics Committee for Human use of Nagasaki University (project registration number: 14051404). Written consent forms were available in Japanese to ensure comprehensive understanding of the study objectives, and informed consent was provided by the participants.
The study population comprised 617 male residents aged 60–69 years from the Western rural communities of Goto city and Saza town, who undertook a general medical checkup from 2013 to 2015 as recommended by the Japanese government. Persons with missing laboratory measurement data (n = 44) and smoking status data (n = 1) were excluded from the study population. To avoid the influence of inflammatory disease and hematological disease, subjects with high and low white blood cell count (≥1,000 cells/μL) (n=8) and 1,000 cells/μL< (n=2), respectively) were also excluded. Additionally, since a decline in glomerular filtration rate (GFR) was identified as a marker of chronic kidney disease (CKD), this should act as a confounding factor in the present study, and we therefore excluded 85 subjects with CKD. The remaining participants, comprising 477 men with a mean age of 65.4 years (standard deviation (SD) 2.6, range 60–69), were enrolled in the study. Hypertension, diabetes, hypercholesterolemia, and current smoker status are regarded as traditional cardiovascular risk factors . Given that renal function, alcohol consumption, and hepatic enzyme levels are also important risk factors for the incidence of stroke [21, 22], and hyperuricemia is associated with carotid atherosclerosis , we also recognize these factors as being related to the known cardiovascular risk factors.
Data collection and laboratory measurements
Body weight and height were measured with an automatic body composition analyzer (BF-220; Tanita, Tokyo, Japan), and body mass index (BMI; kg/m2) was calculated. Systolic and diastolic blood pressures were recorded at rest. Hypertension was defined as a systolic blood pressure ≥140 mmHg and/or a diastolic blood pressure ≥90 mmHg and/or taking antihypertensive medication, as described in previous studies [24, 25], since hypertension defined under these parameters was reported to be associated with the incidence of stroke and coronary artery disease in the Japanese population .
Fasting blood samples were collected in an EDTA-2K tube, a heparin sodium tube and a siliconized tube. The levels of white blood cells in samples from the EDTA-2K tube were measured at SRL, Inc (Tokyo, Japan).
Fresh samples (within 24 h of collection) from a heparin sodium tube were used to determine the number of CD34-positive cells. BD (Beckton Dickinson Biosciences, Franklin Lakes, New Jersey, USA) Trucount™ technology, an accurate and reproducible single platform assay conforming to the International Society of Hematotherapy and Graft Engineering (ISHAGE) guidelines [26, 27] and supported by automated software on the BD FACSCantoTM II system was used to measure the number of circulating CD34-positive cells. Serum samples were separated to measure the concentration of aspartate aminotransferase (AST) and γ-glutamyltranspeptidase (γ-GTP) using the Japanese Society Clinical Chemistry (JSCC) standardized method. Serum creatinine was measured enzymatically. HDL and low-density lipoprotein-cholesterol (LDL) were measured using a direct method, while hemoglobin A1c (HbA1c) was measured using the latex coagulation method. Serum uric acid (UA) was measured enzymatically using the uricase peroxidase (POD) method.
GFR was estimated by means of an established method that was recently proposed by the working group of the Japanese Chronic Kidney Disease Initiative . According to this adapted version, GFR (mL/min/1.73 m2) = 194 × (serum creatinine (enzyme method))−1.094 × (age)−0.287. CKD is defined as a GFR < 60 mL/min/1.73 m2.
Differences in mean values or prevalence of potential confounding factors based on circulating CD34-positive cell levels were calculated. An age-adjusted trend test was performed with a regression model for mean values, and a logistic regression model was used for proportion. Since the number of circulating CD34 cells should indicate the presence of underlying endothelial repair activity [6, 14,15,16,17,18] and 0.99 cells/μL was the median value of the circulating CD34-positive cells in our present study, this value was set as the cutoff point, as in our previous study . Logistic regression models were used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) to determine the influence of HDL on hypertension, and subjects were stratified according to the level of circulating CD34-positive cells (high, low). To avoid the influence of medication on HDL values, we also calculated ORs and 95% CIs of hypertension for increments of one standard deviation (SD) in ORs and 95% CIs stratified by circulating CD34-positive levels (high, low) limited to subjects not taking lipid-lowering medication.
Adjustments for confounding factors that we defined as known cardiovascular risk factors were made in three ways. First, we adjusted only for age. Second, we made a further adjustment for BMI based on the following: BMI has been reported to be positively associated with the level of circulating CD34-positive cells, which is divided by median values of such cells among the general population , and inversely associated with circulating CD34-positive cells predominantly among subjects with a high BMI (31.6 ± 5.1 kg/m2) . In addition, unlike other cardiovascular risk factors, BMI is reported to be inversely associated with HDL-cholesterol  and positively associated with hypertension . Therefore, BMI might act as the strongest confounding factor in the present study. Finally, for the third adjustment, we included other possible confounding factors, including Age (year) and BMI (kg/m2), smoking status (never smoker, former smoker, current smoker), alcohol consumption [never drinker, former drinker, current drinker (23 g/week ≤ <46 g/week, 46 g/week ≤ <69 g/week, 69 g/week≤)], HbA1C (%), LDL (mg/dL), AST (IU/L), γ-GTP (IU/L), UA (mg/dL) and GFR (mL/min/1.73 m2).
All statistical analyses were performed using the SAS system for Windows (version 9.4; SAS Inc., Cary, NC). All p values for statistical tests were two-tailed, with values of <0.05 regarded as being statistically significant.
Characteristics of the study population
Characteristics of the present study population are shown in Table 1. Compared to subjects with a low level of CD34-positive cells, those with high levels demonstrated a significantly higher prevalence of taking antihypertensive medication as well as higher values for BMI, LDL, HbA1c, and WBC.
Association between HDL and hypertension in total subjects and after stratification by circulating CD34-positive cell levels
Table 2 shows the ORs and 95% CIs for hypertension in relation to HDL in all subjects and as well as those in subjects stratified by circulating CD34-positive cell levels. No significant association between HDL-cholesterol and hypertension in total subjects was noted. Analysis of subjects with high levels of CD34-positive cells, however, showed that although HDL had no significant association with hypertension in an age-adjusted model, a significant positive association was observed after further adjustment for BMI. This association was unchanged even after further adjusting for known cardiovascular risk factors. Additionally, among subjects with a low level of CD34-positive cells, a tendency toward an association between HDL and hypertension was observed, although this was not significant. Even after limiting the analysis to subjects not taking lipid-lowering medication (201 men with a high level of CD34-positive cells and 210 men with low CD34-positive cells), the associations remained unchanged. Age-adjusted, age- and BMI-adjusted, and fully adjusted ORs and 95% CIs of hypertension for increments of one standard deviation (SD) in HDL (13.8 mg/dL) were 1.24 (0.95, 1.62), 1.40 (1.05, 1.86), and 1.44 (1.06, 1.96) for subjects with a high level of circulating CD34-positive cells; and 0.89 (0.68, 1.17), 1.00 (0.75, 1.33), and 0.87 (0.63, 1.19) for subjects with low circulating CD34-positive cells.
Association between HDL level and two circulating CD34-positive cell categories on hypertension
An investigation into the effects of the association between HDL level and the two CD34-positive cell categories (high and low) on hypertension revealed a significant interaction; p values for the effect of this interaction were p = 0.034 for the age-adjusted model, p = 0.025 for the age- and BMI-adjusted model, and p = 0.022 for the fully adjusted model.
The major findings of the present study are that, independent of known cardiovascular risk factors, HDL is significantly positively associated with hypertension among subjects with a high level of CD34-positive cells but not for subjects with low CD34-positive cells.
A previous Japanese cross-sectional study of 1803 apparently healthy men aged 49.9 ± 9.0 reported a positive association between HDL and hypertension; the adjusted OR and 95% CI of a 1 mg/dL increment of HDL for hypertension was 1.03 (1.02, 1.04, p < 0.001) . Results of this study are compatible with our present study. Moreover, we found further evidence that the positive association is limited to subjects with a high level of CD34-positive cells.
Furthermore, in our present study, although statistical power did not reach significance initially for subjects with a high level of CD34-positive cells, after further adjusting for BMI, the association between HDL and hypertension became significant. Since HDL is significantly inversely correlated with BMI (r = −0.27, p < 0.001) and a higher BMI is a well-known independent risk factor for hypertension , the unfavorable influence of HDL might be masked by the favorable influence of lower BMI status.
The precise mechanism of action governing the association between HDL concentration in the blood and CD34-positive cells on hypertension risk is not understood. One plausible explanation for such an association is the inhibition of endothelial nitric oxide synthetase (eNOS) by HDL-cholesterol.
Bone marrow-derived endothelial progenitor cells such as CD34-positive cells have been reported to contribute to endothelial repair [11,12,13]. Endothelial cells establish an instructive vascular niche that reconstitutes hematopoietic stem and progenitor cells though the release of specific paracrine growth factors . Since stimulation of CD34-positive cell production in the bone marrow is induced by damage to the endothelium, the number of circulating CD34-positive cells should increase as a result . Therefore, subjects with a high level of CD34-positive cells should demonstrate elevated endothelial repair activity induced by endothelial damage. Previous studies reporting the association of limb ischemia and acute myocardial infarction with a rapid increase in circulating endothelial progenitor cells might partly support this mechanism [34, 35].
In addition to the above, unlike HDL from healthy individuals, HDL from participants with stable cardiovascular disease or acute coronary syndrome inhibits the eNOS-activating pathway and eNOS-dependent nitric oxide (NO) production that leads to loss of endothelial anti-inflammatory effects and endothelial repair . Although HDL exerts vascular-protection via endothelial progenitor cells , our present study found a slight but significant inverse correlation between HDL and log CD34-positive cells for subjects with a high level of CD34-positive cells (r = −0.13, p = 0.047) but not for subjects with low CD34-positive cells (r = −0.09, p = 0.158).
Therefore, among subjects with a high level of CD34-positive cells, HDL values should indicate the magnitude of these unfavorable influences on endothelial repair. The number of circulating endothelial progenitor cells is reported to be inversely correlated with the risk factors for coronary artery disease , and the Framingham risk score  also should support this mechanism.
Since hypertension and endothelial dysfunction have a bidirectional association in which hypertension induces increased arterial stiffness and vice versa [4,5,6,7,8,9,10], an unfavorable influence on endothelial repair should cause hypertension among subjects with a high level of CD34-positive cells.
When an endothelial injury is mild, the necessity of endothelial repair is small, resulting in a low concentration of circulating CD34-positive cells. Since subjects with a small number of CD34-positive cells might have lower endothelial repair activity induced by endothelial injury, HDL should stimulate endothelial cell NO production  and promote endothelial repair mechanisms . In subjects with a low level of CD34-positive cells, HDL should act as it does in healthy individuals. Therefore, in our present study, although the statistical power was not significant, an inverse tendency was observed between HDL and hypertension for subjects with a low level of CD34-positive cells.
Potential limitations of this study warrant consideration. Although hypertension and endothelial dysfunction have a bidirectional association, no data on the evaluation of endothelial function was available. To clarify the background mechanism of the association between HDL and hypertension in relation to circulating CD34-positive cell levels, further analysis that includes endothelial function-related data such as flow-mediated dilation (FMD) will be necessary. Although HDL demonstrates an inverse tendency with hypertension among subjects with a low level of CD34-positive cells, the statistical power did not reach significance. Further investigation with a larger sample population will be necessary. Finally, because this was a cross-sectional study, causal relationships were not able to be established.
In conclusion, we found that HDL is significantly positively associated with hypertension among subjects with a high level of CD34-positive cells but not among subjects with low CD34-positive cells. These results demonstrate an efficient tool for risk estimation of HDL on cardiovascular events.
Body mass index
Chronic kidney disease
Endothelial nitric oxide synthetase
Glomerular filtration rate
International Society of Hematotherapy and Graft Engineering
Japanese Society Clinical Chemistry
Sodium lauryl sulfate
Serum uric acid
Kitamura A, Yamagishi K, Imano H, Kiyama M, Cui R, Ohira T, Umesawa M, Muraki I, Sankai T, Saito I, Iso H; CIRCS Investigators. Impact of hypertension and subclinical organ damage on the incidence of cardiovascular disease among Japanese residents at the population and individual levels. The Circulatory Risk in Communities Study (CIRCS). Circ J. 2017. [Epub ahead of print].
Emerging Risk Factors Collaboration, Di Angelantonio E, Sarwar N, Perry P, Kaptoge S, Ray KK, Thompson A, Wood AM, Lewington S, Sattar N, Packard CJ, Collins R, Thompson SG, Danesh J. Major lipids, apolipoproteins, and risk of vascular disease. JAMA. 2009;302:1993–2000.
Oda E, Kawai R. High-density lipoprotein cholesterol is positively associated with hypertension in apparently healthy Japanese men and women. Br J Biomed Sci. 2011;68:29–33.
Dohi Y. Hypertension and oxidative stress. Nagoya Med J. 2010;51:153–8 [Article in Japanese].
Higashi Y, Sueda T, Yoshizumi M. Role of angiotensin II-related oxidative stress and nitric oxide in endothelial function in hypertension. J Jpn Coll Angiol. 2003;43:47–52 [Article in Japanese].
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Nagayoshi M, Kadota K, Kawashiri SY, Inoue K, Nagata Y, Maeda T. Platelets and circulating CD34-positive cells as an indicator of the activity of the vicious cycle between hypertension and endothelial dysfunction in elderly Japanese men. Atherosclerosis. 2017;259:26–31.
Shimizu Y, Nakazato M, Sekita T, Kadota K, Arima K, Yamasaki H, Takamura N, Aoyagi K, Maeda T. Association between the hemoglobin levels and hypertension in relation to the BMI status in a rural Japanese population: the Nagasaki islands study. Intern Med. 2014;53:435–40.
Shimizu Y, Nakazato M, Sekita T, Kadota K, Yamasaki H, Takamura N, Aoyagi K, Maeda T. Association between hemoglobin levels and arterial stiffness for general Japanese population in relation to body mass index status: the Nagasaki islands study. Geriatr Gerontol Int. 2014;14:811–8.
Shimizu Y, Kadota K, Nakazato M, Noguchi Y, Koyamatsu J, Yamanashi H, Nagayoshi M, Nagata S, Arima K, Maeda T. Hemoglobin as a possible biochemical index of hypertension-induced vascular damage. J Physiol Anthropol. 2016;35:4.
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Nagayoshi M, Kadota K, Kawashiri SY, Maeda T. Possible mechanism underlying the association between higher hemoglobin level and hypertension in older Japanese men. Geriatr Gerontol Int. 2017. [in press].
Walter DH, Rittig K, Bahlmann FH, Kirchmair R, Silver M, Murayama T, Nishimura H, Losordo DW, Asahara T, Isner JM. Statin therapy accelerates reendothelialization: a novel effect involving mobilization and incorporation of bone marrow-derived endothelial progenitor cells. Circulation. 2002;105:3017–24.
Majka M, Janowska-Wieczorek A, Ratajczak J, Ehrenman K, Pietrzkowski Z, Kowalska MA, Gewirtz AM, Emerson SG, Ratajczak MZ. Numerous growth factors, cytokines, and chemokines are secreted by human CD34(+) cells, myeloblasts, erythroblasts, and megakaryoblasts and regulate normal hematopoiesis in an autocrine/paracrine manner. Blood. 2001;97:3075–85.
Shi Q, Rafii S, Wu MH, Wijelath ES, Yu C, Ishida A, Fujita Y, Kothari S, Mohle R, Sauvage LR, Moore MA, Storb RF, Hammond WP. Evidence for circulating bone marrow-derived endothelial cells. Blood. 1998;92:362–7.
Taguchi A, Matsuyama T, Moriwaki H, Hayashi T, Hayashida K, Nagatsuka K, Todo K, Mori K, Stern DM, Soma T, Naritomi H. Circulating CD34-positive cells provide an index of cerebrovascular function. Circulation. 2004;109:2972–5.
Taguchi A, Matsuyama T, Nakagomi T, Shimizu Y, Fukunaga R, Tatsumi Y, Yoshikawa H, Kikuchi-Taura A, Soma T, Moriwaki H, Nagatsuka K, Stern DM, Naritomi H. Circulating CD34-positive cells provide a marker of vascular risk associated with cognitive impairment. J Cereb Blood Flow Metab. 2008;28:445–9.
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Nagayoshi M, Kadota K, Maeda T. Height is an indicator of vascular maintenance capacity in older men. Geriatr Gerontol Int. 2016. [Epub ahead of print]
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Nagayoshi M, Kadota K, Maeda T. Platelets as an indicator of vascular repair in elderly Japanese men. Oncotarget. 2016;7:44919–26.
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Nagayoshi M, Kadota K, Maeda T. Circulating CD34-positive cells, glomerular filtration rate and triglycerides in relation to hypertension. Atherosclerosis. 2015;243:71–6.
Besler C, Heinrich K, Rohrer L, Doerries C, Riwanto M, Shih DM, Chroni A, Yonekawa K, Stein S, Schaefer N, Mueller M, Akhmedov A, Daniil G, Manes C, Templin C, Wyss C, Maier W, Tanner FC, Matter CM, Corti R, Furlong C, Lusis AJ, von Eckardstein A, Fogelman AM, Lüscher TF, Landmesser U. Mechanisms underlying adverse effects of HDL on eNOS-activating pathways in patients with coronary artery disease. J Clin Invest. 2011;121:2693–708.
Kim YD, Jung YH, Saposnik G. Traditional risk factors for stroke in East Asia. J Stroke. 2016;18:273–85.
Shimizu Y, Maeda K, Imano H, Ohira T, Kitamura A, Kiyama M, Okada T, Ishikawa Y, Shimamoto T, Yamagishi K, Tanigawa T, Iso H. Chronic kidney disease and drinking status in relation to risks of stroke and its subtypes: the Circulatory Risk in Communities Study (CIRCS). Stroke. 2011;42:2531–7.
Shimizu Y, Imano H, Ohira T, Kitamura A, Kiyama M, Okada T, Sato S, Shimamoto T, Yamagishi K, Tanigawa T, Iso H. gamma-Glutamyltranspeptidase and incident stroke among Japanese men and women: the Circulatory Risk in Communities Study (CIRCS). Stroke. 2010;41:385–8.
Shimizu Y, Sato S, Koyamatsu J, Yamanashi H, Tamai M, Kadota K, Arima K, Yamasaki H, Takamura N, Aoyagi K, Maeda T. Subclinical carotid atherosclerosis and hyperuricemia in relation to renal impairment in a rural Japanese population: the Nagasaki Islands study. Atherosclerosis. 2014;233:525–9.
Shimizu Y, Nakazato M, Sekita T, Kadota K, Yamasaki H, Takamura N, Aoyagi K, Kusano Y, Maeda T. Association between alkaline phosphatase and hypertension in a rural Japanese population: the Nagasaki Islands Study. J Physiol Anthropol. 2013;32:10.
Shimizu Y, Yoshimine H, Nagayoshi M, Kadota K, Takahashi K, Izumino K, Inoue K, Maeda T. Short stature is an inflammatory disadvantage among middle-aged Japanese men. Environ Health Prev Med. 2016;21:361–7.
Sutherland DR, Anderson L, Keeney M, Nayar R, Chin-Yee I. The ISHAGE guidelines for CD34+ cell determination by flow cytometry. International Society of Hematotherapy and Graft Engineering. J Hematother. 1996;5:213–26.
Barnett D, Janossy G, Lubenko A, Matutes E, Newland A, Reilly JT. Guideline for the flow cytometric enumeration of CD34+ haematopoietic stem cells. Prepared by the CD34+ haematopoietic stem cell working party. General Haematology Task Force of the British Committee for Standards in Haematology. Clin Lab Haematol. 1999;21:301–8.
Imai E, Horio M, Watanabe T, Iseki K, Yamagata K, Hara S, Ura N, Kiyohara Y, Moriyama T, Ando Y, Fujimoto S, Konta T, Yokoyama H, Makino H, Hishida A, Matsuo S. Prevalence of chronic kidney disease in the Japanese general population. Clin Exp Nephrol. 2009;13:621–30.
Müller-Ehmsen J, Braun D, Schneider T, Pfister R, Worm N, Wielckens K, Scheid C, Frommolt P, Flesch M. Decreased number of circulating progenitor cells in obesity: beneficial effects of weight reduction. Eur Heart J. 2008;29:1560–8.
Pietrobelli A, Lee RC, Capristo E, Deckelbaum RJ, Heymsfield SB. An independent, inverse association of high-density-lipoprotein-cholesterol concentration with nonadipose body mass. Am J Clin Nutr. 1999;69:614–20.
Oda E, Kawai R. Body mass index is more strongly associated with hypertension than waist circumstance in apparently healthy Japanese men and women. Acta Diabetol. 2010;47:309–13.
Kobayashi H, Butler JM, O’Donnell R, Kobayashi M, Ding BS, Bonner B, Chiu VK, Nolan DJ, Shido K, Benjamin L, Rafii S. Angiocrine factors from Akt-activated endothelial cells balance self-renewal and differentiation of haematopoietic stem cells. Nat Cell Biol. 2010;12:1046–56.
Inoue T, Sata M, Hikichi Y, Sohma R, Fukuda D, Uchida T, Shimizu M, Komoda H, Node K. Mobilization of CD34-positive bone marrow-derived cells after coronary stent implantation: impact on restenosis. Circulation. 2007;115:553–61.
Takahashi T, Kalka C, Masuda H, Chen D, Silver M, Kearney M, Magner M, Isner JM, Asahara T. Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization. Nat Med. 1999;5:434–8.
Shintani S, Murohara T, Ikeda H, Ueno T, Honma T, Katoh A, Sasaki K, Shimada T, Oike Y, Imaizumi T. Mobilization of endothelial progenitor cells in patients with acute myocardial infarction. Circulation. 2001;103:2776–9.
Petoumenos V, Nickenig G, Werner N. High-density lipoprotein exerts vasculoprotection via endothelial progenitor cells. J Cell Mol Med. 2009;13:4623–35.
Vasa M, Fichtlscherer S, Aicher A, Adler K, Urbich C, Martin H, Zeiher AM, Dimmeler S. Number and migratory activity of circulating endothelial progenitor cells inversely correlate with risk factors for coronary artery disease. Circ Res. 2001;89:E1–7.
Hill JM, Zalos G, Halcox JP, Schenke WH, Waclawiw MA, Quyyumi AA, Finkel T. Circulating endothelial progenitor cells, vascular function, and cardiovascular risk. N Engl J Med. 2003;348:593–600.
Mineo C, Yuhanna IS, Quon MJ, Shaul PW. High density lipoprotein-induced endothelial nitric-oxide synthase activation is mediated by Akt and MAP kinases. J Biol Chem. 2003;278:9142–9.
Noor R, Shuaib U, Wang CX, Todd K, Ghani U, Schwindt B, Shuaib A. High-density lipoprotein cholesterol regulates endothelial progenitor cells by increasing eNOS and preventing apoptosis. Atherosclerosis. 2007;192:92–9.
We are grateful to the staff from Goto City Hall and Saza Town Hall for their outstanding support.
This study was supported by Grants-in-Aids for Scientific Research from the Japan Society for the Promotion of Science (No. 25291107 and No. 15 K07243).
Availability of data and materials
The individual raw data will not be shared publicly because of the ethics policy.
YS designed the study and performed the statistical analyses, interpreted the data, and drafted the manuscript or revised it. SS, JK, HY, MN, KK, and SK assisted with the design of the study, were involved in data collection, and checked the manuscript. SS, JK, SK, and TM participated in the study concept and checked the manuscript. TM was the general coordinator and also designed the study. All authors read and approved submission of the manuscript, and that material in the manuscript has not been published and is not being considered for publication elsewhere in whole or in part in any language except as abstract. The person in acknowledgement has been seen and approved mentions of his name in the article. All authors have read and approved the submission of the manuscript and that material in the manuscript has not been published in whole or in part in any language except as an abstract. The persons mentioned in this section have seen and approved the mention of their names in this article.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the Ethics Committee for Human Use of Nagasaki University (project registration number 0501120073). Written consent forms were available in Japanese to ensure comprehensive understanding of the study objectives, and informed consent was signed by the participants.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Shimizu, Y., Sato, S., Koyamatsu, J. et al. Association between high-density lipoprotein-cholesterol and hypertension in relation to circulating CD34-positive cell levels. J Physiol Anthropol 36, 26 (2017). https://doi.org/10.1186/s40101-017-0143-9
- Circulating CD34-positive cell