Research Article | Open Access
Guorong Gu, Weizhong Cheng, Chenling Yao, Jun Yin, Chaoyang Tong, Andrew Rao, Lawrence Yen, Matthew Ku, Jianyu Rao, "Quantitative Proteomics Analysis by Isobaric Tags for Relative and Absolute Quantitation Identified Lumican as a Potential Marker for Acute Aortic Dissection", BioMed Research International, vol. 2011, Article ID 920763, 10 pages, 2011. https://doi.org/10.1155/2011/920763
Quantitative Proteomics Analysis by Isobaric Tags for Relative and Absolute Quantitation Identified Lumican as a Potential Marker for Acute Aortic Dissection
Acute aortic dissection (AAD) is a serious vascular disease. Currently the diagnosis relies on clinical and radiological means whereas serum biomarkers are lacking. The purpose of this study was to identify potential serum biomarkers for AAD using isobaric tags for relative and absolute quantitation (iTRAQ) approach. A total of 120 serum samples were collected from three groups: AAD patients (), patients with acute myocardial infarction (AMI, ), and healthy volunteers (), whereas the first 10 samples from each group were used for iTRAQ analysis. Using iTRAQ approach, a total of 174 proteins were identified as significantly different between AAD patients and healthy subjects. Among them, forty-six proteins increased more than twofold, full-scale analysis using serum sample for the entire 120 subjects demonstrated that Lumican level was significantly increased relative to control and AMI samples. Further, Lumican level correlated with time from onset to admission in AAD but not AMI samples. Using iTRAQ approach, our study showed that Lumican may be a potential AAD-related serum marker that may assist the diagnosis of AAD.
Acute aortic dissection (AAD) has become a treatable disease due to recent advances in new therapeutic approaches for the management of heart and arterial diseases; however, development of quick and economic diagnostic methods remains a challenge. Variability in disease presentation often obscures diagnoses, and imaging modalities such as computed tomography (CT), magnetic resonance imaging (MRI), and esophagus ultrasound remain prohibitive due to cost and availability. Aortic dissection remains a frequent target of medicolegal litigations with accusations of failure to diagnose against treating physicians and hospitals . Some progress in the biochemical diagnosis of AAD has been made in the last decade [2, 3]; several acute phase proteins and coagulation parameters were identified to increase in AAD patients, but these are nonspecific biomarkers for AAD as they may be also aberrantly expressed in other disease conditions such as acute myocardial infarction (AMI).
Recently a quantitative proteomic assay, isobaric tags for relative and absolute quantitation (iTRAQ), has been developed and utilized to identify biomarkers for various disease conditions [4, 5]. This chemical labeling method involves the stable incorporation of isotopes into an amine tagging reagent, which can then be reliably detected by mass spectrometry, thereby permitting comparative quantitation of various proteins in a multiplex manner. It has been suggested to be suitable for the discovery of biomarkers in a wide range of body fluids and tissues, including serum and plasma [5, 6]. With this method, we expect to find the potential biomarkers which are released from the disruption of the aortic media and can provide sufficient specificity and longer time window for the diagnosis of AAD.
2. Materials and Methods
The study included a total of 30 healthy individuals and 90 patients (60 AAD, 30 AMI). All the patients were selected in a consecutive manner from the period of July 2009 to November 2011 from Fudan University affiliated Zhongshan Hospital (Shanghai, China). iTRAQ analysis was performed for the first twenty patients (10 AAD and 10 AMI) and ten healthy individuals. All patients presented within 72 hours after an episode of chest and/or back pain lasting 5 minutes or more. The diagnosis of AAD was confirmed by computed tomographic arteriography (CTA). The AMI patient was confirmed by electrocardiography (ECG) and cardiac troponin T (cTNT) tests. All patients gave their informed consent for the study. The protocol was approved by the Ethics Committee of Zhongshan Hospital.
For each study subject, whole blood samples were immediately collected in BD Vacutainer SST tubes (BD Diagnostics, Plymouth, UK) after admission and centrifuged at 4000 rpm for 10 min at room temperature. The serum was frozen and stored in aliquots at −80°C until analysis.
2.2. Serum C-Reactive Protein and Myoglobin Test
Vitros 5.1 FS automatic biochemistry analyzer (Johnson & Johnson; Calif, USA) was used for serum C-reactive protein (CRP) test, and Cobas e411 immunoassay analyzer (Roche; Mannheim, Germany) was used for the serum myoglobin (Myo) test. The results were then interpreted in accordance with that tested by the International Federation of Clinical Chemistry (IFCC) recommended method. Analyses were performed immediately after the centrifugation of whole blood samples.
2.3. iTRAQ Sample Preparation: Strong Cation Exchange (SCX) Chromatography
iTRAQ reagents were purchased from Applied Biosystems (Foster City, USA). Fourteen interfering highly abundant proteins from serum samples were removed using Agilent multiple affinity removal liquid chromatography (LC) column-Human 14 (MARS) (shimadzu, Kyoto, Japan). One hundred micrograms of each extract were precipitated using acetone at −20°C and suspended in 20 μL of dissolution buffer (Applied Biosystems, Foster City, USA). After reduction and alkylation, each sample was digested with trypsin (w(trypsin) : w(protein) = 1 : 20) at 37°C overnight. The tryptic peptides were labeled with the iTRAQ reagents as follows: normal controls group was labeled with iTRAQ 113, AMI group was labeled with iTRAQ 114, and AAD group was labeled with iTRAQ 115. The peptides were pooled and desalted with Sep-Pak Vac C18 (Waters, Milford, USA). The peptide mixture was diluted with buffer A containing 10 mM KH2PO4 in 25% acetonitrile (ACN) at pH 2.6. The peptides were fractionated by 20AD high-performance liquid chromatography (HPLC) system (Shimadzu; Kyoto, Japan) equipped with a polysulfoethyl A column (2.1 mm × 100 mm, 5u, 200 A; The Nest Group, Southborough, Mass). The composition of buffer B was 350 mM KCl, 10 mM KH2PO4, and 25% ACN at pH 2.6. Separation was performed using a linear binary gradient of 0–80% buffer B in buffer A at a flow rate of 200 μL/min for 60 min. The fractions were combined into 20 groups.
2.4. LC-MS Analysis
Each SCX fraction was dried down by the rotary vacuum concentrator, dissolved in buffer C (0.1% formic acid, 5% ACN, 95% water), and analyzed on Qstar XL (Applied Biosystems; Foster City, USA). The HPLC gradient was 5–35% buffer D (95% ACN, 0.1% formic acid) in buffer C at a flow rate of 300 nL/min for 70 min. Analysis survey scans were acquired MS from m/z 400–1800 with up to 4 precursors selected for MS/MS from m/z 100–2000.
2.5. The Confirmative ELISA Analysis for Lumican
The confirmative ELISA analysis for Lumican was performed using the kits from CUSABIO BIOTECH CO, following manufacture’s recommendation (CUSABIO BIOTECH CO., LTD., Wuhan, China).
2.6. Data Analysis
All statistical analyses were performed in SPSS 12.0 (SPSS Inc. Chicago, USA). Results were presented as Mean ± SD. A comparative analysis of multiple groups was performed with a one-way-ANOVA or Mann-Whitney/Kruskal-Wallis Test. Statistical significance was defined as . Peptide and protein identification was performed by searching the MS/MS spectra against the SwissProt database using the local Protein Pilot 2.0.1 software. Only peptides identified with confidence interval values of no less than 95% (Unused ProtScore >1.3) were used for protein identification compilation and subsequent quantitation calculation. Fold changes of >2 or <0.5 were set as cut-off values to designate significant differences in protein expression among the AAD group and the normal control group.
2.7. PANTHER Analysis
The PANTHER database was used to elucidate cellular components, biological processes, and the molecular functions associated with each individual protein (http://www.pantherdb.org/).
3.1. Clinical Features of Study Subjects
The clinical features of the AAD patients, AMI patients, and normal controls are summarized in Table 1. There were no differences in age distribution and sex composition among the three groups involved either for ELISA analysis () ( and 0.378, resp.,) or iTRAQ analysis ( and 0.873, resp.). There was no differences in the time from onset to admission between AAD and AMI group either ().
a One-way-ANOVA; bChi-square Test; cMann-Whitney Test.|
3.2. Functional Classification of Identified Proteins by iTRAQ
A total of 174 proteins with confidence interval values of no less than 95% were identified (Unused ProtScore > 1.3). However, after manually rechecking the MS/MS data thoroughly peak by peak, 155 proteins (89.08%) had a relative quantitation of one or more peptides. Fifteen proteins had no quantifiable peptides that could be ascertained, and four proteins had peptides with confidence interval values that were less than 95%.
In total, 174 proteins were sorted using the PANTHER classification system, which sorts the proteins into respective categories based on their molecular functions. The major groups include: signaling molecules (13%), enzyme modulators (12%), transfer/carrier proteins (11%), and proteases (10%). Other groups include: structural proteins (1%), cell adhesion molecules (1%), cytoskeletal proteins (3%), extracellular matrix proteins (2%), and cell junction proteins (1%).
As a way to cross-check the reliability of quantitation of iTRAQ reagent, serum CRP and Myo levels were assessed using both conventional biochemical and immunoassay tests and iTRAQ analysis on the same specimens. With biochemical and immunoassay analysis, CRP was 41.31 ± 32.76 mg/mL and Myo was 66.42 ± 81.23 mg/mL in AAD group, while in normal controls, the former was 5.88 ± 1.42 and the latter was 32.07 ± 14.14 mg/mL. CRP and Myo levels of AAD patients were 7.03-fold and 2.07-fold higher, respectively, than normal controls. Using iTRAQ, the AAD/normal controls ratios of CRP and Myo were similar at 9.12-fold (Table 2) and 1.47-fold. The ratios of CRP and Myo among three groups were similar with either biochemical and immunoassay or iTRAQ analysis, confirming the reliability of iTRAQ analysis.
a Unused > 1.3 means at least 95% confidence; bnumber of peptides with 95% confidence; AAD: acute aortic dissection; AMI: acute myocardial infarction; CON: normal controls.|
3.3. Proteins with Over Twofold Differential Expression
A total of 155 proteins had a relative quantitation difference for AAD patients compared with the normal control group of which 46 proteins increased more than twofold (Table 2), while 36 proteins decreased more than twofold among the AAD patients (Table 3). Among the identified proteins with increased levels in AAD, there were a number of acute phase reactants (CRP, Beta-2-microglobulin, Complement factor I), blood coagulation marker (Haptoglobin, Coagulation factor V, Coagulation factor IX), and cellular components (Lumican, Tubulin beta-3 chain, Fibronectin). However when compared to AMI patients, 14 of the 46 protein showed less than 2-fold increase, including complement component 9, complement factor1, Plasma protein C1 inhibitor, and Ig Kappa chain C-region (Table 2). Interestingly, some acute phase proteins such as CRP remains on the list as it showed the differential expression between the two conditions.
a Unused > 1.3 means at least 95% confidence; bnumber of peptides with 95% confidence; AAD: acute aortic dissection; AMI: acute myocardial infarction; CON: normal control.|
Among proteins with decreased expression in AAD patients compared with normal controls, there were a number of molecules involved in protein metabolism (Inter-alpha-trypsin inhibitor heavy chain H2, Alpha-2-HS-glycoprotein), lipid metabolic process (Apolipoprotein A-IV, Apolipoprotein E, Apolipoprotein C-I), blood coagulation marker (Fibrinogen alpha chain, Prothrombin), and cellular components (Alpha-2-HS-glycoprotein, thrombospondin-1 (TSP-1)). When compared to AMI patients, 8 of 36 proteins did not reach the 2-fold differential expression (Table 3).
3.4. The ELISA Analysis of Serum Concentrations of Lumican
Based on the iTRAQ findings above we selected two targets, Fibronectin and Lumican, the protein markers potentially associated with vascular injury, for the validation using ELISA method. At the initial analysis using 10 AAD and 10 normal samples we found that statistical significant difference between AAD and normal individual was seen for Lumican but not Fibronectin (data not shown). Therefore, we carried a full validation study only for Lumican, using the entire 120 samples collected (see Table 1). A statistical significant difference between AAD, AMI, and normal individual was seen in serum concentrations of Lumican (2.66 ± 4.58 ng/mL in AAD group, 0.69 ± 0.34 ng/mL in AMI group, and 0.85 ± 0.53 ng/mL in normal control, ). The difference for AAD and AMI also reached statistical significance () suggesting the specificity of this marker for AAD (Figure 1). We further analyzed the correlation between Lumican levels with time from onset of symptoms to admission. As shown in Figure 2, a correlation was seen in AAD group (, ) but not in AMI group (, ), further confirming the specificity of Lumican as a marker for AAD.
iTRAQ analysis is recently been used as a potentially more effective biomarker discovery method than traditional proteomic methods. The high reproducibility optimizes this technique for embarking on “fishing-expeditions” as an initial screening for potential useful biomarkers [6–8]. As a means of internal validation, the iTRAQ method was compared with CRP biochemical assay and Myo immunoassay. In our study there were no significant differences in the serum levels determined by the different methods. Thus, the iTRAQ method we employed appears in this preliminary analysis to be suitable for the detection of relevant proteins.
To identify differentially expressed proteins, in many studies, the cut-off points were set at 20% to 50% average variance [7, 9, 10]. However, such approaches may result in finding markers with low specificity [2, 3]. We therefore appropriated to increase the cut-off point at 100% variance in serum levels of candidate proteins between AAD patients and normal subjects. Thus, only twofold changes below or above normal controls were considered significant. In our study, total of 155 proteins had a relative difference between AAD patients and healthy volunteers. Therefore, with higher specificity, these candidate proteins are more likely to be potential biomarkers for AAD.
In the group of significantly increased proteins, there were numerous acute phase reactants, such as Beta-2-microglobulin (P61769), which could be indicative of an increased inflammatory response among AAD patients. CRP (P02741), a protein found to be elevated in patients who presented with symptoms or rupture of AAD and abdominal aortic aneurysm, was also identified using iTRAQ [11, 12]. CRP is a nonspecific biomarker associated with AAD and a predictor for long-term adverse events , and it can be used to monitor evolution of false lumen thrombosis . Unfortunately, CRP is also produced in coronary plaques , acute myocardial infarction , and so forth. The elevations of these acute phase reactants represent a generalized reaction to vascular injury, and as such, they are nonspecific biomarkers. In addition, many proteins identified are associated with blood coagulation and fibrinolytic system. Among which, ten had increased serum levels (e.g., P00450-Ceruloplasmin, P02751-Fibronectin, P00738-Haptoglobin…), and twelve had decreased serum levels (e.g., P02671-Fibrinogen alpha chain, P00751-Complement factor B, P00734-Prothrombin…). The pathophysiological mechanism for the appearance of these proteins may be explained by the release of tissue factors from the dissected aortic wall then the activation of the extrinsic coagulation system [17–19]. In addition, platelets can be activated by injuries to the vessel wall, activation of the coagulation cascade, or by activating factors released from stimulated endothelial cells and platelets (e.g., ADP, thromboxane, von Willebrand Factor). It also has been found that platelet functions were affected secondary to acute massive consumption coagulopathy in the false lumen in AAD patient [20, 21].
In the past few years, extracellular matrix (ECM) components of vessel walls such as elastin have been shown to be elevated in aortic dissections; however, such increases were less than twofold . Our study found 9 extracellular matrix component proteins with greater than twofold differences, among these are Carboxypeptidase (P22792), Lumican (P51884), Fibronectin (P02751), Ceruloplasmin (P00450), and Thrombospondin-1 (TSP-1, P07996). Fibronectin is a polymorphic and multifunctional glycoprotein that plays wide-ranging roles in tissue injury [22–25]. TSP-1, which is an extracellular protein that participates in cell-to-cell and cell-to-matrix communication, can stimulate or inhibit the migration of vascular smooth muscle cells or endothelial cells. It has been known as a plasma marker of peripheral arterial disease .
Lumican is distributed in interstitial collagenous matrices throughout the body. In coronary arteries ischemic lesion, it is overexpressed by vascular smooth muscle cells (VSMCs)  and also synthesized in aortic smooth muscle cells . In iTRAQ analysis, serum Lumican levels in patients with AAD were 1.29-fold and 3.63-fold higher than in patients with AMI and normal controls, respectively. It is interesting to note that with iTRAQ analysis, the level of difference between AAD and AMI for Lumican is less than that of Fibronectin (Table 2), yet the initial validation using ELISA method showed that only Lumican was significantly increased in AAD and AMI samples. While there may be variety reasons to explain the variations of the findings between the two methods, it highlights the importance of validation in biomarker studies. The finding that Lumican expression correlated with the time from onset to admission only in AAD but not in AMI sample further confirmed the specificity of this protein in association with AAD.
Proteomic approach provides an exciting platform to identify clinically useful protein biomarkers. As an initial step our study identified potential candidate protein biomarkers in the serum of AAD patients with the iTRAQ technique. However, the ultimate development of biomarkers which provide sufficient sensitivity or specificity for the diagnosis of AAD will require multiple validations and clinical testing, which may include nonprotein markers. Nevertheless our findings provide preliminary list of candidate biomarkers that should be further validated, either alone or in combination.
In this paper, we found that iTRAQ technique is a suitable approach for the detection of the new potential protein markers in the serum of AAD patients. Using iTRAQ approach, our study identified that Lumican may be a potentially interesting new serum marker of AAD, and upon further validation this marker may assist the clinical diagnosis of AAD.
This study was supported by Shanghai Committee of Science and Technology (114119a9000). The authors also thank the Department of Chemistry and the Institute of Biomedical Science, Fudan University, Peoples Republic of China, for providing support for the project.
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