NOS2polymorphisms associated with the susceptibility to pulmonary arterial hypertension with systemic sclerosis: contribution to the transcriptional activity
© Kawaguchi et al.; licensee BioMed Central Ltd. 2006
Received: 22 February 2006
Accepted: 2 June 2006
Published: 3 July 2006
Systemic sclerosis (SSc) is a connective tissue disease characterized by tissue fibrosis. One of several complications of SSc, pulmonary arterial hypertension (PAH) can be refractory to treatment, both novel and established. In the present study we investigated the ratio of circulating nitric oxide to endothelin-1 in patients with both SSc and PAH, and determined whether polymorphisms in NOS2 (the nitric oxide synthase 2 gene) are associated with susceptibility to PAH. Endothelin-1 in plasma and nitric oxide metabolites (nitrate and nitrite) in serum were measured. The nitric oxide/endothelin-1 ratio was significantly lower in patients with both SSc and PAH than in patients with SSc only or in healthy control individuals. We confirmed the presence of two single nucleotide polymorphisms at positions -1,026 and -277 and a pentanucleotide repeat (CCTTT) at -2.5 kilobases. There were significant differences in single nucleotide polymorphisms between patients with SSc who had PAH and those who did not, and between patients with both SSc and PAH and healthy control individuals. The CCTTT repeat was significantly shorter in patients with both SSc and PAH than in patients with SSc only or in healthy control individuals. Transcriptional activity were analyzed using the luciferase reporter assay. The transcriptional activity of NOS2 was much greater in fibroblasts transfected by a vector with a long allele of the CCTTT repeat than in those transfected by a vector with a short allele. Polymorphisms in the NOS2 gene are associated with transcriptional activity of the NOS2 gene and with susceptibility to SSc-related PAH.
Systemic sclerosis (SSc) is an autoimmune disease of unknown aetiology that is characterized by extensive fibrosis of skin and visceral organs, and dysfunction of vascular tone . In its more severe forms, cardiac involvement and respiratory involvement are the most significant determinants of outcome . In particular, pulmonary hypertension is a fatal complication in both diffuse and limited cutaneous SSc . Pulmonary hypertension is generally divided into four major categories: pulmonary arterial hypertension (PAH), pulmonary hypertension associated with left-sided heart disease, pulmonary hypertension associated with lung disease or hypoxaemia, and pulmonary hypertension due to chronic thrombotic or embolic disease . A major part of pulmonary hypertension as it pertains to SSc corresponds with the pathophysiology of PAH, a disease of the small pulmonary arteries characterized by vascular proliferation, vasoconstriction, remodelling of the pulmonary vessel wall and thrombosis in vessels.
Vasodilators such as nitric oxide (NO) and prostacyclin, along with prolonged overexpression of vasoconstrictors such as endothelin (ET)-1, not only affect vascular tone but also promote vascular remodelling, both of which have been implicated in the pathogenesis of PAH [5–12]. Previous studies identified high levels of ET-1 in the plasma of patients with SSc, especially in those with SSc complicated by PAH [13, 14]. However, reported levels of circulating NO in patients with SSc are inconsistent, with several studies [15–18] finding increased levels of NO in patients with SSc and others [19, 20] finding low levels, similar to those in healthy individuals. In our previous study  NO levels were markedly elevated in patients with early-stage diffuse cutaneous SSc, especially when the SSc was accompanied by active alveolitis, but concentrations of NO in serum were low in late-stage limited cutaneous SSc. No patients suffered the complication of PAH in that study. Characteristic levels of NO and NO/ET-1 ratio in patients with both SSc and PAH remain to be established.
NO is an endothelial-derived relaxing factor that is synthesized from L-arginine by nitric oxide synthase (NOS) . Three isoforms of NOS have been identified : NOS-1 (neuronal NOS), NOS-2 (inducible NOS) and NOS-3 (endothelial NOS). NOS-2 is the major source of NO production in conditions involving exposure to cytokines; this is because it is induced by a variety of cell types, including the proinflammatory cytokines interleukin-1, tumour necrosis factor-α, interferon-γ, and ET-1 .
Two randomized, double-blind, placebo-controlled trials [25, 26] evaluated the efficacy of the ET receptor antagonist bosentan in patients with PAH that was either primary or associated with SSc. Another therapeutic strategy in PAH is to increase the activity of endogenous NO, which enhances NO-dependent cGMP-mediated pulmonary vasodilatation through inhibition of the breakdown of cGMP by phosphodiesterase type 5 . Although long-term inhaled NO therapy has shown only a small benefit in patients with PAH , phosphodiesterase type 5 inhibitors (for example, sildenafil) have been found to improve pulmonary artery pressure in patients with PAH .
Because these novel therapies were developed to prolong survival and improve patients' quality of life, we speculate that an imbalance between ET-1 and NO is key to the pathogenesis of SSc complicated by PAH. Polymorphisms in the NOS2 gene promoter are thought to regulate its transcription activity, which is reportedly associated with susceptibility to type 1 diabetes  and atopy  and with protection against malaria . In the present study we determined the levels of ET-1 and NO in blood from patients with SSc with or without PAH, and we investigated the association between gene polymorphisms in NOS2 and susceptibility to PAH.
Materials and methods
Clinical characteristics of patients
Number at entry (n (male:female)
Age (years; mean (range)
Diffuse SSc:limited SSc (n)
Disease duration (months; mean (range)
Pulmonary fibrosis (n (%)
Frequency of ANA (n (%)
Anti-topoisomerase I antibody
We identified the presence of a complication of PAH in the following manner. All patients with SSc were first evaluated by Doppler echocardiography, and then cardiac catheterization was performed when right ventricular systolic pressure was greater than 30 mmHg, based on Doppler echocardiography. PAH was diagnosed in patients with SSc who satisfied the modified US National Institutes of Health criteria for PAH after cardiac catheterization , specifically mean pulmonary artery pressure above 25 mmHg at rest or 30 mmHg after exercise, with normal pulmonary artery wedge pressure. The complication of pulmonary fibrosis was identified using high-resolution computed tomography of the chest. Patients with the following complications were excluded: severe pulmonary fibrosis, with functional vital capacity below 70%; left-sided heart disease; chronic thrombotic or embolic disease; renal failure, including a history of scleroderma renal crisis; hypertension; and diabetes.
Measurement of plasma endothelin-1 and serum nitric oxide levels
Blood samples were obtained from 16 patients with both SSc and PAH and from 26 patients with SSc without PAH who were randomly selected from among patients with SSc who donated DNA samples at the time of admission to Aoyama Hospital with informed consent. No specific diet was given to patients while they were hospitalized. Twenty healthy volunteers (normal control individuals) who had no history of dieting or smoking gave informed consent to participate in the study and gave blood samples. ET-1 levels were measured in plasma using an enzyme-linked immunosorbent assay kit (R&D Systems, Cambridge, MA, USA). Because serum NO is quickly degraded into nitrite and nitrate, we measured the total levels of these NO metabolites as indicators of NO level, using a calorimetric assay kit (Cayman Chemical, Ann Arbor, MI, USA).
Sequencing the NOS2promoter region
Genomic DNA was extracted from the blood sample using a DNA extraction kit (Qiagen, Valencia, CA, USA). For direct sequencing, PCR was performed to amplify the promoter region of the NOS2 gene from -100 to -1,335 bp. The forward and reverse primers were 5'-TCATCCACACATTCACTCAAC-3' and 5'-CCAAAGGGAGTGTCCCCAGCTT-3', respectively. The sequences of the PCR products were analyzed using the ABI Prism 3100 Sequence Detection System (Applied Biosystems, Foster City, CA, USA).
Haplotype typing in pairs of NOS2polymorphisms
We entered the genotype data into the PENHAPLO computer program, developed by Ito and coworkers , to estimate haplotype frequency in the population and to calculate the posterior probability of diplotype distribution for each study subject. This program was designed for haplotype typing using a maximum likelihood estimation method based on the expectation maximization algorithm under the assumption of Hardy-Weinberg equilibrium for the population.
Analysis of variable numbers of the CCTTT repeat polymorphism of the NOS2promoter region
Genomic DNA was amplified by PCR with the use of a FAM™-labelled sense primer (5'-ACCCCTGGAAGCCTACAACTGCAT-3') and an antisense primer (5'-GCCACTGCACCCTAGCCTGTCTCA-3'). The various alleles were resolved by capillary electrophoresis on an ABI Prism 3100 Genetic Analyzer System (Applied Biosystems). Allele sizes were calculated using the GeneScan Analysis computer program, with a GeneScan™-500 ROX™ size standard (Applied Biosystems) as the internal size standard.
Analysis of transcriptional activity of NOS2in human fibroblasts
Human fibroblasts from three healthy individuals were cultured in Dulbecco's modified Eagle's medium (DMEM) with 10% foetal bovine serum (FBS; Sigma, St. Louis, MO, USA). For transient transfections, fibroblasts were cultured in six-well plates with 3 ml Opti-MEM (Invitrogen) containing 4 μg DNA (pGL3 and phRL-TK vectors) and 12 μl Lipofectamine 2000 (Invitrogen). After 4 hours, 3 ml DMEM with 20% FBS in the presence or absence of recombinant interleukin-1β (10 ng/ml; R&D Systems) was added. The medium was changed after 16 hours to DMEM with 10% FBS in the presence or absence of interleukin-1β (5 ng/mL). After an additional 24 hours of culture, the cells were washed twice using cold phosphate-buffered saline and were harvested. Firefly and Renilla luciferase activities were measured using the Dual-Glo Luciferase Assay System (Promega). Fibroblasts were cotransfected with a constitutively active Renilla luciferase vector (phRL-TK), and firefly luciferase activity was normalized by Renilla luciferase activity.
Circulating ET-1 and NO concentrations are given as mean ± standard deviation, and data were compared using the Student's t test. We assessed the significance of the -277A/G and -1026G/T single nucleotide polymorphisms (SNPs) by the Fisher exact test. The relationship between the NO/ET-1 ratio and summed CCTTT repeat length was analyzed using linear regression analysis. An allelic distribution of the number of CCTTT repeats was compared using the Mann-Whitney U test. P < 0.05 was considered statistically significant.
Circulating endothelin-1 and nitric oxide concentrations
Determination of single nucleotide polymorphisms in the NOS2promoter region
Haplotype typing of the NOS2promoter region
Distribution of single nucleotide polymorphisms in NOS2 gene promoter region
SSc with PAH (n = 20)
SSc without PAH (n = 58)
Healthy controls (n = 95)
Distribution of variable numbers of tandem repeat in the NOS2promoter region
Allele frequencies for the CCTTT-repeat polymorphism
Effects of NOS2polymorphisms on transcriptional activity of the gene
In the present study were found that concentrations of NO metabolites were not increased in patients with both SSc and PAH, although plasma ET-1 levels were markedly elevated. Our previous report  indicates that serum levels of NO metabolites were significantly higher in patients with SSc than in healthy control individuals, especially in patients with a diffuse cutaneous type, active fibrosing alveolitis, or a short duration since onset. However, the population considered in that study did not include patients with PAH, which could explain why the present findings are inconsistent with those of the previous report. Although a number of reports have been published concerning concentrations of ET-1 or NO in the circulation of patients with SSc [8, 13–21], this report is the first to describe an imbalance in the NO/ET-1 ratio in patients with PAH.
Over the past decade abnormalities in NO synthesis have been proposed as being important in the pathogenesis and development of pulmonary hypertension, especially primary pulmonary hypertension (PPH). Initially, immunohistochemical studies showed that pulmonary hypertension was associated with diminished expression of NOS-3 . However, other studies found increase in expression of NOS-3 in patients with pulmonary hypertension and in animal models of pulmonary hypertension [38, 39]. Despite these contradictory findings, it has been reported that NO levels in blood and the lungs were precisely decreased in patients with PPH and collagen disease related PAH [8–12]. Furthermore, it was determined that NOS-dependent endogenous NO synthesis was decreased in patients with PPH, which suggests that NOS activity may be diminished in patients with PPH . Lung inflammation leading to increased levels of cytokines and oxidants may contribute to the development of both PPH and SSc-related PAH . In the presence of increased levels of inflammatory mediators, NOS activity may be dependent on production of NOS-2, which is distinct from NOS-3 (the endothelial form of NOS) because NOS-2 is inducible by inflammatory mediators, and induced levels are much greater than levels of constitutive NOS-3 production. Peripheral mononuclear cells and lesional fibroblasts are capable of aberrant production of inflammatory cytokines in patients with SSc [42–44]. These cytokines may be involved not only in ET-1 synthesis by endothelial cells and fibroblasts but also in induction of NOS-2. Also, excessive production of ET-1 can mediate NOS-2 production through ET receptor B . Although evidence based on those biological properties may promote speculation that levels of ET-1 correlate with levels of NO in the circulation, NO metabolite levels were within normal range in patients with both SSc and PAH patients whose serum contained much ET-1. We hypothesize that this discrepancy may be explained by reduced NOS-2 production resulting from polymorphisms in the NOS2 gene.
As a result of sequencing the promoter region of the NOS2 gene from -100 to -1,335, we were able to confirm the presence of two SNPs, consistent with previous reports . In the present study, allele A at -277 SNP, allele G at -1,026 SNP and shorter forms of the CCTTT repeat were associated with susceptibility to PAH combined with SSc. The number of CCTTT repeats was previously reported to influence transcription of the NOS2 gene . However, studies of variable numbers of tandem repeat both in vitro and in vivo have yielded conflicting results . To confirm whether those polymorphisms affect transcription of the NOS2 gene in fibroblasts, we constructed a series of luciferase reporter vectors cloned by various numbers of CCTTT combined with the promoter region of the NOS2 gene from +58 to -1,557, which included two kinds of haplotype.
Transcriptional activity was lowest in the NOS2 gene containing the six repeats of CCTTT and haplotype GA, which suggests that transcription of the NOS2 gene might be little induced by interleukin-1β in patients with SSc-related PAH.
Irrespective of whether patients with SSc had PAH, CCTTT repeat length was well correlated with NO/ET-1 ratio. With regard to the relationship between CCTTT repeat length and serum NO levels, we found no significant difference among SSc patients without PAH, although there were significant differences among all SSc patients and among patients with both SSc and PAH (data not shown). In the setting of aberrant production of ET-1 or cytokines, NO synthesis via NOS-2 induction may be dependent on NOS2 gene polymorphisms. In healthy control individuals, who had no vascular damage, inflammation, or autoimmune disorders, there was no association between CCTTT repeat length and either serum NO levels or NO/ET-1 ratios (data not shown). Because NOS-2 induction is well controlled by ET-1 and cytokines, distinct from NOS-3, which is constitutively produced, it has been suggested that the CCTTT repeat length is more significantly correlated with NO/ET-1 ratios than with serum NO levels. Our observations support the concept that the NOS2 gene polymorphism is a crucial factor in NO synthesis under conditions of vascular damage and chronic inflammation, as well as PAH.
It is not possible to determine whether SSc patients without PAH will suffer this complication in the future, and this is a limitation of the present study. The patients enrolled in the study are from a prospective cohort at our institution, and they have been observed for clinical complications, including PAH, in the follow-up clinic. None of the 58 patients with SSc but not PAH has yet been diagnosed with PAH (mean duration of observation: 45 months).
NO is a key factor in generating PAH complicated by SSc, and the decrease in NO synthesis might be attributable to reduced NOS-2 production, which is dependent on NOS2 gene polymorphisms. Therapeutic options for PAH occurring as a complication of SSc are limited; however, it is not usually the first complication, and it develops several years after SSc is diagnosed. We believe that the development of means to predict the occurrence of PAH related to SSc, and hence prevent this complication, would be a great step forward. Although prospective, longitudinal studies are needed, we propose that patients with SSc who exhibit an imbalance between NO and ET-1 production and who have a short length of CCTTT repeat of the NOS2 gene can be treated with a phosphodiesterase type 5 inhibitor before the occurrence of PAH.
= base pairs
= Dulbecco's modified Eagle's medium
= foetal bovine serum
= nitric oxide
= nitric oxide synthase
= pulmonary arterial hypertension
= polymerase chain reaction
= primary pulmonary hypertension
= single nucleotide polymorphism
= systemic sclerosis.
This study was supported in part by the Japanese Ministry of Health, Labour and Welfare grant (the research for Mixed Connective Tissue Disease) and the Research for the Future Program of the Japan Society for the Promotion of Science.
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