Y chromosome loss is associated with age-related male patients with abdominal aortic aneurysms
Authors Tang D, Han Y, Lun Y, Jiang H, Xin S, Duan Z, Zhang J
Received 19 January 2019
Accepted for publication 15 April 2019
Published 23 July 2019 Volume 2019:14 Pages 1227—1241
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 3
Editor who approved publication: Dr Zhi-Ying Wu
Dianjun Tang,*,1,2 Yanshuo Han,*,3 Yu Lun,1 Han Jiang,1 Shijie Xin,1 Zhiquan Duan,1 Jian Zhang1
1Department of Vascular Surgery, The First Hospital of China Medical University, Key Laboratory of Pathogenesis, Prevention and Therapeutics of Aortic Aneurysm Liaoning Province, Shenyang, People’s Republic of China; 2Department of Vascular Surgery, The Second Hospital of Shandong University, Jinan, People’s Republic of China; 3Department of General Surgery, Shengjing Hospital of China Medical University, Shenyang, People’s Republic of China
*These authors contributed equally to this work
Purpose: Abdominal aortic aneurysm (AAA) demonstrates many features of autoimmune diseases. Y chromosome, sex-determining region of the Y chromosome (SRY) gene, androgen receptor (AR) gene, and androgen appear as potential candidates for influence of the male immune function. This study investigated Y chromosome numbers, SRY gene, AR gene, and androgen levels in male AAAs. We also investigated the correlation between Y chromosome loss (LOY) ratio, SRY expression, androgen levels, and age.
Patients and methods: We investigated LOY by fluorescence in situ hybridization (FISH) in 37 AAAs and compared with 12 patients with abdominal aortic atherosclerotic occlusive disease (AOD) and 91 healthy controls (HC). We investigated SRY and AR expression at mRNA level by real-time PCR in peripheral T lymphocytes in AAA compared with AOD and HC, and AR protein levels by immunohistochemistry (IHC) in AAA. LOY, SRY expression, androgen levels, and age were examined for correlations using the Spearman’s rank correlation coefficient.
Results: LOY ratio in peripheral T lymphocytes was significantly higher in the AAA group compared with the HC (9.11% vs 5.56%, P<0.001) and AOD groups (9.11% vs 6.42%, P=0.029). The SRY mRNA expression in peripheral T lymphocytes was 4.7-fold lower expressed in the AAA group than in the HC group (P<0.001). Free plasma testosterone levels were lower in the AAA group compared with the HC group (P=0.036), whereas sex hormone-binding globulin levels were higher (P=0.020). LOY ratio and expression of SRY mRNA level increased with age in the AAA group (R=0.402 and, R=0.366, respectively). A significant correlation between AR mRNA level (R=0.692) and aortic diameter was detected. Simultaneously, in AAA tissue, the rate of LOY increased with age (R=0.547) and also positively associated with LOY in peripheral blood T lymphocytes (R=0.661).
Conclusion: This study identified a prominent Y chromosome loss in male AAAs, which is correlated to age, lower level of SRY expression and free testosterone, providing a new clue for the mechanisms of AAA.
Keywords: abdominal aortic aneurysm, age-related, Y chromosome, sex-determining region of the Y chromosome (SRY), testosterone
Abdominal aortic aneurysm (AAA) is a major cause of morbidity and mortality in western countries,1,2 the incidence and prevalence of which in China have increased significantly during the last two decades.3 Despite surgical advances, the recent interest in developing new therapies for treating small asymptomatic, nonoperation-indicated AAA has led to greater efforts to investigate and define its cellular and molecular nature. Increasing evidence suggests that the immune response contributes to the development of aneurysmal diseases, and AAAs demonstrate many features of autoimmune diseases, including genetic predisposition, organ specificity, and chronic inflammation.4,5 It is well documented that infiltrating T cells are essentially always present in AAA lesions, and AAA is likely a specific autoimmune T-cell disease.6 Besides, a striking gender difference exhibited in AAA patients revealed a male: female ratio of up to 4:1, and male sex is one of the strongest risk factors for AAA.7 Pathogenetic hypotheses include possible roles for androgen, environmental triggers, and genetic susceptibility.
The genetic influence on AAA initially focused on the relevance of autosomal genes, and possible susceptibility gene(s) have been identified in rare cases of AAAs with familial tendencies.8,9 However, most AAAs are sporadic, and no relevant genetic factors have yet been identified in these cases. Sex chromosomes have been recently investigated in terms of loss of mosaicism, reactivation, and haploinsufficiency in numerous autoimmune diseases and cancers, and other diseases demonstrating sexual dimorphism.10–14 The Y chromosome contains many genes related to sex determination, hormone generation, and fertility, but also harbors several X homologs, which might exert relevant roles in immune function.15 The sex-determining region of the Y chromosome (SRY) gene includes a high-mobility group domain, a conserved motif present in many DNA-binding proteins, which could be involved in the regulation of multiple functions such as postnatal steroidogenesis and spermatogenesis.16
A recent large population-based study of Australian men showed that patients with AAA had lower free and total testosterone levels than men without AAA.17 Furthermore, levels of free testosterone were inversely correlated with AAA, suggesting that decreased levels of testosterone were associated with aortic dilation. These results challenge previous ideas that androgens play a pathogenetic role in vascular physiology and pathophysiology and promote the development of AAA,17,18 indicating the need for more studies examining the role of the male sex chromosome in AAA.
In this study, we investigated Y chromosome numbers in T lymphocytes and aneurysmal tissue in men with AAA. We also detected mRNA expression of SRY and androgen levels anf investigated the correlation between SRY, AR expression, and age.
Materials and methods
AAA population selection
Between January 2009 and December 2018, a total of 364 AAA patients registered in China Medical University aneurysm Biobank (CMUaB) and China Medical University aneurysm blood Biobank (CMUabB) were selected to this study, which were obtained from the Department of Vascular Surgery of the First Hospital of China Medical University (CMU) and Department of General Surgery of Shengjing Hospital of CMU. The AAA tissue specimen, peripheral blood samples, and corresponding clinical data were collected from these patients consecutively, after aneurymal open surgery (OSR). Simultaneously, peripheral blood samples and related clinical data were extracted within these patients consecutively, after endovascular repair (EVAR).
Inclusion criteria for AAA patients in this study were: 1) male patients with an infrarenal abdominal aorta diameter above 30 mm or larger than 1.5–2 times the diameter of the abdominal aorta in their normal segment diagnosed by three-dimensional computed tomography angiography (3D-CTA);19 2) availability of corresponding patient history and clinical data, including history of ruptured, history of coronary and peripheral artery disease, medication history, and the presence of risk factors of atherosclerosis, such as smoking habits, hypertension, diabetes mellitus, or hyperlipidemia. Exclusive criterion: male AAA patients with Ehlers–Danlos syndrome, Marfan syndrome, and other known vascular disorders were excluded. None of the patients had any evidence or medical history of other autoimmune diseases.
AAA tissue specimen
126 patients from CMUaB were examined by an experienced vascular surgeon within 2 days before and after the OSR. Until December 2018, nine patients not willingly and openly reveal their inpatients of information via publication, whether their clinical data, aneurymal tissue, or blood sample. Finally, aneurysm specimens from 96 male patients were eligible for further analyses. Here, AAA tissue specimen (n=17) and corresponding peripheral blood samples (n=17) were obtained who underwent OSR. All samples were harvested at the most dilated place of aortaventralis, by which tissues in vitro were washed in PBS (Boster, Wuhan, China), opened transversely, and fixed in 4% paraformaldehyde (Beijing Chemical Works, Beijing, China) for 24 hrs. The samples were then embedded in paraffin and sectioned transversely at 2–3 µm continuously to make parallel sections. Immunofluorescence was stained by anti-CD3 monoclonal antibody (BD Biosciences, San José, CA, USA) to identify T lymphocytes on one section for cell type analysis and localization and the other was prepared for fluorescence in situ hybridization (FISH).
AAA peripheral blood samples
A total of 338 patients from CMUabB were examined by an experienced vascular surgeon within 2 days before and after the EVAR. Until December 2018, 29 patients discarded reveal their inpatients' information, eg, clinical data, blood laboratory results, and blood sample. Finally, aneurysm specimens from 254 male AAA patients were eligible for further analyses. The androgen level in serum sample, total RNA extraction and chromosome preparations in peripheral blood mononuclear cell (PBMC) we need to performed, both serum and PMBC samples were obtained successfully in 20 male AAA patients who underwent EVAR shown in Figure 1. Blood was obtained preoperatively from patients and controls between 5 and 6 o’clock in the early morning in 10-mL anticoagulant tubes, with three tubes per sample.
Normal control population selection
The normal control group comprised age-matched healthy control males (HCs) (n=91, 50–84 years old, aorta diameter 16.9–25.8 mm), selected from a healthy population who received annual regular physical examinations. HCs had a relatively healthy peripheral vascular system determined by ultrasonography, and there was no evidence or medical history of aneurysm, abdominal aortic atherosclerotic occlusive disease (AOD), or other vascular disorders. Other exclusion criteria were cancer, infection, and any other immune-mediated disease. We collected clinical data, blood laboratory results, and blood samples from the HC group as controls.
AOD population selection
Because AAA patients also had prominent atherosclerosis, we selected a second control group of age-matched men with infrarenal AOD from our hospital (n=12, 49–79 years, aorta diameter 14.8–25.6 mm), with no medical history of aneurysmal disease, other vascular disorders, connective tissue disorders, or known autoimmune diseases. AOD was diagnosed by enhanced CT scanning or 3D-CTA. This group was used to control for any potential involvement of atherosclerosis in the possible autoimmune mechanisms, especially in early lesions. We collected clinical data, blood laboratory results, and blood samples from the AOD group as another control.
Ethics approval and consent to participate
Written informed consent was obtained from AAA patients, AOD patients, and controls in the study, before tissue and blood sampling. This study was performed according to the Guidelines of the World Medical Association Declaration of Helsinki and was approved by the local ethics committee of the China Medical University. The selection process of the corresponding patients is summarized in Figure 1.
Peripheral blood mononuclear cell (PBMC) extraction and T-cell preparation
PBMCs were extracted by Ficoll-sodium diatrizoate (Ficoll-Hypaque, Haoyang TBD, Co, Tianjin, China) density-gradient centrifugation. After several washing steps with PBS, PBMCs were allowed to adhere to the plastic for 2 hrs at 37°C to deplete monocytes. Floating cells were collected and expression of CD3 in fresh peripheral blood lymphocytes was evaluated by flow cytometry (FACSCalibur; BD Biosciences) using PerCP-conjugated anti-CD3 monoclonal antibody (BD Biosciences) to identify the population of T lymphocytes. Each sample contained >90% CD3+ T lymphocytes at the time of assessment (Figure 2).
Figure 2 Purity of isolated T cells as determined by flow cytometry in blood samples of AAA (A), AOD (B), and HC (C).Abbreviations: AOD, aortic atherosclerotic occlusive disease; HC, healthy controls; AAA, abdominal aortic aneurysm.
Serum was prepared after centrifuge of blood and stored at −80°C until assayed. Total serum levels of testosterone, dehydroepiandrosterone (DHS), and sex hormone-binding globulin (SHBG) were determined by chemiluminescent immunoassays using Immulite 2000 total testosterone, Immulite 2000 DHEA-SO4, and Immulite 2000 SHBG assays (Siemens Healthcare Diagnostics Products Limited, Llanberis, UK) on an Immulite 2000 analyzer (Siemens Healthcare Diagnostics, Flanders, USA). Free testosterone was determined by chemiluminescent immunoassay using free testosterone in vitro diagnostic kits (Snibe, Shenzhen, China) on a Maglumi 4000 analyzer (Snibe). The working ranges for total testosterone, DHS, SHBG, and free testosterone were 0.7–55 nmol/L, 0.41–27 µmol/L, ≤180 nmol/L, and 0.50–150.0 pg/mL, respectively. The sensitivities were 0.5 nmol/L, 0.08 µmol/L, 0.02 nmol/L, and 0.5 pg/mL, respectively, and the reference values were 6.27–26.28 nmol/L, 2.17–15.20 µmol/L, 13.00–71.00 nmol/L, and 55.05–183.50 pmol/L, respectively, according to the Institute of Endocrinology, the First Affiliated Hospital of China Medical University.
Chromosome preparations and FISH analysis
T lymphocytes were separated from peripheral blood (AAA, n=37; AOD, n=12; HC, n=91) and prepared as follows. Cytology Pepsin Solution (Zytovision, Bremen, Germany) was applied to the cytology specimens and incubated for 5 mins at 37°C in a humidity chamber. The slides were then incubated in 1% wash buffer Tris-HCl buffer solution (TBS) 1% formaldehyde solution, and again in 1× wash buffer TBS (Zytovision) for 5 mins each, dehydrated in 70%, 90%, and 100% ethanols for 1 min each, and then air dried. Ten microliters of CENX/Yq12 dual-color probe (Zytovision) was pipetted onto each individual sample, covered with a coverslip (22 mm×22 mm), and sealed with rubber cement (Zytovision). The slides were denatured at 72±1°C for 2 mins on a hot plate, transferred to a humidity chamber (Abbott, Chicago, USA), and hybridized overnight at 37°C. The cement and coverslip were removed the following day using Cytology Stringency Wash Buffer SSC (Zytovision) for 2 minss at 72±1°C for 1 min at room temperature. Thirty microliters of DAPI (Zytovision) was then pipetted onto the slides, covered with a coverslip (24 mm×60 mm), avoiding trapped bubbles, and incubated in the dark for 15 mins.
T lymphocytes of AAA tissue specimen (n=17) were prepared as follows. Cytology Pepsin Solution (Zytovision) was applied to the cytology specimens and incubated for 10 mins at 37°C in a humidity chamber, followed by incubation in 1× wash buffer TBS, 1% formaldehyde solution, and 1× wash buffer TBS (Zytovision) for 5 mins each; dehydrated in 70%, 90%, and 100% ethanols for 1 min each, and then air dried. Ten microliters of CENX/Yq12 dual-color probe (Zytovision) was pipetted onto each individual sample, covered with a coverslip (22 mm ×22 mm), and sealed with rubber cement (Zytovision). The slides were denatured at 83±1°C for 2 min on a hot plate, transferred to a humidity chamber (Abbott), and hybridized overnight at 37°C. The rubber cement and coverslip were removed carefully the following day using Cytology Stringency Wash Buffer SSC (Zytovision) for 2 mins at 72±1°C for 1 min at room temperature. Thirty microliters of DAPI (Zytovision) was then pipetted onto the slides, covered with a coverslip (24 mm×60 mm) avoiding trapped bubbles, and incubated in the dark for 15 mins.
All samples were analyzed under an Olympus Bx51 microscope equipped with DAPI and Fluorescein isothiocyanate-Tetramethyl isothiocyanate (FITC-TRITC) epifluorescence optics and a digital camera by two independent observers, who were blinded to the patient’s characteristics. Hybridization signals were captured using a CytoVision system (Leica Biosystems, Nussloch, Germany). At least 500 nuclei were scored for each sample, and the Y chromosome loss rate was expressed as a percentage (%) of the total number of nuclei counted.
RNA extraction and real-time PCR
To study SRY and androgen receptor (AR), total RNA was isolated from peripheral T lymphocytes (AAA, n=32; AOD, n=12; HC, n=54) using Trizol reagent (Invitrogen, Carlsbad, CA, USA), according to the manufacturer’s protocol. RNA quality and quantity were assessed by NanoDrop ND-1000 (Thermo Fisher Scientific, Waltham, MA, USA) analysis of 260/280 ratios. High-quality RNA samples were obtained with an A260/A280 ratio >1.8. RNA was treated with DNase I (Takara, Dalian, China) before reverse transcription to eliminate contaminating genomic DNA. Total RNA was reverse transcribed with reverse transcriptase (PrimeScript RT Reagent Kit; Takara) and oligo-dT primer, according to the manufacturer’s instructions. Real-time fluorescent quantitative PCR was performed using SYBR-green I Premix Ex Taq (Takara) using the Thermo 9700 Real-Time PCR System (Thermo Fisher), following the manufacturer’s instructions, with ddH2O as a negative control. The primers for glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were 5ʹ-CCACCCATGGCAAATTCCCATGGCA-3ʹ (sense) and 5ʹ-TCTAGACGGCAGGTCAGGTCCACC-3ʹ (anti-sense), which was used as an endogenous control. The primers for SRY were 5ʹ-CGCATTCATCGTGTGGTCT-3ʹ (sense) and 5ʹ-GCCATTTTTCGGCTTCAGTA-3ʹ (anti-sense), primers for AR were 5ʹ-GCAGGAAGCAGTATCCGAAG-3ʹ (sense) and 5ʹ-TTGGCGTTGTCAGAAATGG-3ʹ (anti-sense). Thermal cycle parameters were: 95°C for 30 s for 1 cycle, then 95°C for 5 s, and 60°C for 30 s for 40 cycles. All PCR assays were carried out in duplicate, and data were analyzed with the Thermo 9700 Real-Time PCR System (Thermo Fisher) using the comparative threshold cycle (2−ΔΔCT) method.
Histological, immunohistochemistry (IHC), and immunofluorescence analysis
The AAA fragments were prepared as aforesaid and samples were embedded in paraffin to obtain transverse sections. Serial sections were cut at 2–3 μm and prepared for H&E, immunochemical, and immunofluorescence staining.
Histological evaluation: The quality of each slide was assessed twice independently as follows: no staining (-), weak positive staining (±), scattered positive staining (+), majority positive staining (++), and strong overall positive staining (+++). These score analyses were performed for all cells within the vessel wall and for all specimens. In addition, for interrelated quality evaluation between the abovementioned quality evaluation following scoring was used: +/++ and ++/+++.
IHC analysis: The sections were treated with 3% hydrogen peroxide/methanol (Mai Xin_Bio, Fuzhou, China), followed by incubating with rabbit monoclonal antibody against AR (ab133273,1:100; Abcam, Cambridge, UK) or mouse monoclonal antibody against CD3 (sc-20047, 1:500; Santa Cruz Biotechnology, Shanghai, China) in 2% BSA PBS overnight at 4°C. After being washed with PBS, the sections were incubated with anti-rabbit/mouse IgG-HRP antibody (Boster) for 0.5 hrs at 37°C. Finally, 3,3ʹ-diaminobenzidine (DAB) (Mai Xin_Bio) was used as a chromogen for 10 mins until the brown yellow color appeared. Four visual fields were randomly selected on each slide. Light microscopic results were graded semiquantitatively from 0 (to the corresponding no staining change) to +3 (to the corresponding strong staining change: +++). This histopathological grading was performed for endothelial cells, inflammatory infiltrate, and macrophages in the AAA tissue samples.
Immunofluorescence analysis: The sections were treated with 3% hydrogen peroxide/methanol (Mai Xin_Bio), followed by incubating with rabbit monoclonal antibody against AR (ab133273,1:100; Abcam) or mouse monoclonal antibody against CD3 (sc-20047, 1:500; Santa Cruz Biotechnology) in 2% BSA PBS overnight at 4°C. After being washed with PBS, the sections were incubated with FITC-labelled secondary anti-rabbit/mouse IgG-HRP antibody (Boster) for 0.5 hrs at room temperature in 0.5% BSA/PBS. Coverslips were mounted in Prolong Gold with (DAPI) (Zytovision), then pipetted onto the slides, covered with a coverslip (24 mm×60 mm), avoiding trapped bubbles, and incubated in the dark for 15 mins. All samples were analyzed under an Olympus Bx51 microscope equipped with DAPI and FITC-TRITC epifluorescence optics and a digital camera.
Data were tested by the Shapiro–Wilk’s test and followed a normal distribution. Independent t-test was used for comparisons of normally distributed data and Mann–Whitney U test for not normally distributed data. Pearson’s Chi-square test and Fischer’s exact test were used for normally and not normally distributed categorical variables, respectively. For correlational analyses, correlations between continuous variables were analyzed first through Pearson’s correlation coefficient for normally distributed values or through Spearman’s rank correlation coefficient for nonparametric samples. The correlations between plasma TES, androstenedione (AND), SHBG, DHS, free plasma testosterone (F-TES), diameter, LOY%, and mRNA of SRY were analyzed through partial correlation analysis adjusted by age. Statistical comparisons were performed using SPSS 20.0 (IBM, Chicago, IL, USA). Statistical significance was defined as P<0.05.
Characterization of AAA and AOD patients analysis
The experimental study group included 37 male patients (17 underwent OSR, 20 underwent EVAR) of infrarenal AAA. The youngest AAA subject was 49 years and the oldest 81 years old. Regarding the comparison of the study groups (AAA group vs AOD group vs HC group) as shown in Table 1, no significant differences were observed in age, hypertension, and other indices (all P-value >0.05). As respected, the mean maximum diameter of AAA was 56.6±15.3 mm which was significantly higher than AOD and HC group.
Table 1 Clinical features in patients with AAA, AOD, and healthy controls
As reported, tobacco smoking was a possible risk factor for Y chromosome loss.20 Therefore, a corresponding number of smoking individuals have been selected in control groups to eliminate the possible interference. The individuals were selected to ensure that there was no significant difference in the rate of smokers and smoking index (pack-years) in AAA, AOD, and HC groups (also in Table 1). Smoker was defined in this study as continuous smoking for more than half a year and at least 10 cigarettes per day (WHO1997).
Incidence of LOY and SRY expression in AAA peripheral T lymphocytes
A total of 70,000 interphase nuclei from peripheral T lymphocyte of the 37 male AAA patients, 12 male AOD patients, and 91 male donors were analyzed by in situ hybridization for X and Y hypoploidy, respectively (Figure 3). Y chromosome loss in peripheral T lymphocytes detected by FISH was significantly higher in the AAA group compared with the HC (9.11±3.96% vs 5.56±3.50%, P<0.001) and AOD groups (9.11±3.96% vs 6.42±1.93%, P=0.029). There was no significant difference in Y chromosome loss between AOD groups and HC groups (P=0.253) (Figure 4A). Furthermore, we investigate the correlation between the rate of Y chromosome loss correlate and other baseline factors in AAAs. After logistic regression analysis, there were no significant correlations between LOY and comorbidity such as hypertension, diabetes mellitus, coronary artery disease, and smoking history in patients with AAA (Table S1).
The SRY mRNA expression in peripheral T lymphocytes was 4.7-fold lower expressed in the AAA group than in the HC group (P<0.001). Moreover, SRY mRNA expression in peripheral T lymphocytes was significantly lower in AOD group than in HC group (0.19±0.12 vs 3.94±2.68, P<0.001), but there was no significant difference between the AAA and AOD group (P=0.328) in Figure 4B.
Plasma sex hormone level and androgen receptor level in AAA patients and controls
F-TES levels were lower in the AAA group compared with the HC group (P=0.036), whereas SHBG levels were higher (P=0.020). There was no significant difference between the AAA and HC groups in terms of total testosterone (TEST), DHS, and AND level (Table 2). However, there was no significant difference in the expression of androgen receptor (AR) mRNA level between the AAA group and HC group (P=0.083), AOD group (P=0.140) in Figure 4C.
Table 2 Plasma sex hormone level in AAA patients and controls
Correlations between peripheral LOY and age-related AAA or sex hormone level
In Table 3, peripheral LOY ratio and expression of SRY mRNA level were examined for correlations using the Spearman’s rank correlation coefficient due to the heterogeneous distribution of the experimental data. As respected, the result demonstrated that peripheral LOY ratio was positive significantly correlated with expression of SRY mRNA level (R=0.709, P<0.001) adjusted by age. Second, we analyzed the rate of LOY in peripheral T lymphocytes in relation to continuous age. Y chromosome loss and expression of SRY mRNA level increased with age in the AAA group (R=0.402, P=0.014 and R=0.366, P=0.039S, respectively). In addition, plasma SHBG level correlated significantly with SRY mRNA level (R=0.433, P=0.039) and continuous age in AAA patients (R=0.456, P=0.007). A significant correlation between AR mRNA level (R=0.692, P<0.001) and aortic diameter was detected adjusted by age.
Table 3 Partial correlation analysis of the peripheral T lymphocytes LOY ratio, mRNA expression of SRY and AR, plasma sex hormone level within AAA using partial correlation coefficient
Incidence of LOY and correlations within AR protein level in AAA tissue
To assess the extension of the individual histopathological features in AAA wall (n=17), a semiquantitative histological characterization of all AAA tissue samples was performed (Table 4). There was no significant difference in Y chromosome loss between AAA peripheral blood T lymphocytes and AAA tissues (9.14±3.93% for peripheral T lymphocytes vs 8.08±2.42% for AAA tissue, P=0.460). Regarding the AR protein level, using IHC and immunofluorescence, inflammation cells were strongly positive for AR expression, particularly in T lymphocytes (Figure 5). Furthermore, the semiquantitative histological characterization and the results of LOY ratio were analyzed again by calculating correlation coefficient in order to explore any relationships between aneurymal LOY ratio and AR protein level within AAA tissue. There is no significant correlation between LOY ratio and AR protein level (R=0.052, P=0.844). Interestingly, in AAA tissue, the rate of LOY increased with age (R=0.547, P=0.023) and also positively associated with LOY in peripheral blood T lymphocytes (R=0.661, P=0.004) (Table 5).
Table 4 Overview of the LOY ratio and classification of semiquantitative IHC analysis in AAA tissue (n=17)
Table 5 Correlation analysis of the LOY ratio, mRNA expression of AR in AAA tissue, and peripheral T lymphocytes LOY and peripheral blood parameters using Spearman rank correlation coefficient
The results of the present study provide the first evidence for an association between Y chromosome loss in T lymphocytes and AAA in male patients. Previous studies demonstrated an increased incidence of X monosomy in PBMC of female patients,11,21 and Y chromosome loss in PBMC was investigated in male patients with autoimmune thyroiditis and primary biliary cirrhosis.15,22 Sex chromosome loss is not an exclusively female phenomenon, but it is also associated with disease in the male population. Y chromosome appears as a potential candidate for influence of the immune function in men. Y chromosome loss has been shown to increase with age,23,24 but our findings indicated that the degree of Y chromosome loss in AAA patients exceeded that in HCs, similar to the situation for X chromosome loss in female primary biliary cirrhosis patient populations.11
The reasons for Y chromosome loss remain unknown, though the rate of cellular turnover and a potential increase in Y-loss susceptibility with aging may be involved.6,22 Y chromosome loss has been associated with phenotype in several malignant diseases and has been suggested as a marker predicting response to therapy.24–27 The intrinsic pathophysiologic mechanism is largely unclear. However, loss of one X chromosome could potentially lead to haploinsufficiency of X-linked loci, escaping X chromosome inactivation processes,21,28 and Y chromosome loss may similarly result in an imbalance of alleles shared with the X chromosome.
The Y chromosome mainly harbors genes involved in male sexual development and spermatogenesis.16 However, a number of X chromosome homologs potentially relevant to immune function have recently been identified in pseudoautosomal regions, including the IL-9 receptor (IL-9R) and IL-3 receptor subunit alpha (IL-3RA, CD123) (www.genecards.org). IL-9R is expressed by a series of T lymphocytes, including Th2 cells, Th17, and T-regs,29 and imbalances in this gene might thus affect the suppressive potential of the T-cell compartment. We previously identified deficient Treg function in patients with AAAs,30 which could partly be explained by the present findings. Moreover, the IL-9R gene has also been suggested to be associated with the development of some autoimmune conditions such as asthma.31 IL-3RA is an important marker during maturation of myeloid dendritic cells, which have recently been shown to play an important role in maintaining autoimmune tolerance.32 However, the influence of loss of this gene to on immunoregulation remains to be determined.
The SRY locus is an evolutionarily conserved locus on the mammalian Y chromosome responsible for testis determination and development.33 SRY encodes a transcription factor that acts by binding to and activating the testis-specific enhancer of the related gene SOX9.34 SOX9 is tightly associated with Sertoli cell development.35–37 It is also expressed in postnatal testicular Leydig cells, targeting the proteins involved in steroidogenesis,38 and has been considered to regulate testosterone production.39 We found that SRY expression was significantly decreased as a result of Y chromosome loss in T lymphocytes of AAA patients compared with control groups, which may contribute to the lower total and free testosterone levels in men with AAA identified in the current and previous studies.17
Lower free or total testosterone levels have been associated with higher overall and cardiovascular mortalities in middle-aged and older men. It has previously been linked with atherosclerotic plaque formation. One possible mechanism may be that testosterone depletion may predispose to AAA through loss of the beneficial effects of testosterone on endothelial function, and adverse influences on circulating lipids and vascular inflammation.17,40–42 Emerging evidence43 suggests that testosterone protects against the development of autoimmune conditions such as arthritis and lung disease in male SKG mice, and removal of testosterone increased both lung and joint diseases in male mice. This mechanism may involve the ability of testosterone to modulate the development of antibodies against citrullinated proteins. Occurrence of AAA in female patients is probably involved in a different pathway in which androgen does not take a major role. Accumulating data indicate the protective effect of estrogen in the mechanism of vascular disease including aneurysms.44,45 However, it would be expected that after aging this effect has been largely weakened due to a lower level of female hormone. This may explain the increased occurrence of AAA in aged women.
Our observations establish that, in addition to the immune effects of Y chromosome loss, which may contribute autoimmune injury in AAA, lower SRY expression may downregulate testosterone production, thus weakening its protective role and further contributing to the formation and development of AAA.
There are limitations to this study such as the limited sample size, lack of healthy aorta tissue, and lack of vivo experiment. First, our study comprises a relatively small sample size. As in all studies, especially those with a small sample size, both beta errors (due to small cohorts) and alpha errors (due to multiplicity of comparisons) should be considered. Second, the present study illustrates a correlation between the Y chromosome loss and age-related AAA; temporal relations between LOY and the age within AAA cannot be discerned. Still, as it is the first of its kind in humans, the data do provide important information. The lack of appropriate aortic wall tissue from controls limited the protein expression analysis. Third, this research mainly exploded the difference between AAA, AOD, and HC in LOY. Therefore, the residual blood samples could not be obtained abundantly from these AAA patients or control group, which is insufficient to perform the expression of SRY and AR at mRNA level or protein level after the FISH study. Additional studies are also needed to clarify the relationship between exogenous androgen treatment and the dilation of aortic aneurysm. Even with these potential limitations, our study results are good, providing a new clue for the mechanisms of AAA.
In conclusion, this study demonstrated a significant increase of Y chromosome loss in peripheral T lymphocytes and aneurysm sac wall tissue in male patients with AAAs, accompanied by decreased SRY expression in peripheral T lymphocytes and lower F-TES. Y chromosome loss ratio and expression of SRY mRNA level increased with age in AAA peripheral T lymphocytes. Furthermore, in AAA tissue, the rate of LOY increased with age and also positively associated with LOY in peripheral blood T lymphocytes. These findings indicate a novel clue in AAA mechanisms, and possibly a novel target for personalized treatment of this disease.
This work was supported by National Nature Science Foundation of China (Grant No. 304717076 and 81600370), Nature Science Foundation of Liaoning Province, China (Grant No. 2014021028), and Basic research program of Liaoning provincial institutions of 550 higher learning 2017 (LZDK201701), and China Postdoctoral Science Foundation (Grant No. 2018M640270).
The authors report no conflicts of interest in this work.
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Table S1 The adjusted logistic regression analysis of peripheral T lymphocytes LOY ratio and association with AAA clinical comorbidity
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