The cytokine-driven regulation of secretoglobins in normal human upper airway and their expression, particularly that of uteroglobin-related protein 1, in chronic rhinosinusitis
© Lu et al; licensee BioMed Central Ltd. 2011
Received: 15 October 2010
Accepted: 8 March 2011
Published: 1 December 2011
The involvement of secretoglobins (SCGBs) other than SCGB1A1 (Clara cell 10-kDa protein, CC10) in human airway diseases remains unexplored. Among those SCGBs, SCGB3A2 (uteroglobin-related protein 1, UGRP1) is particularly interesting, given its structure and function similarities with SCGB1A1 (CC10). The aim of this study was to investigate the expression regulation of SCGBs other than SCGB1A1 (CC10) in human upper airway, and their potential involvement, particularly that of SCGB3A2 (UGRP1), in chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP) and without nasal polyps (CRSsNP).
Eight SCGB family members including SCGB3A2 (UGRP1), SCGB1C1 (ligand binding protein RYD5), SCGB1D1 (lipophilin A), SCGB1D2 (lipophilin B), SCGB1D4 (interferon-γ inducible SCGB), SCGB2A1 (mammaglobin 2), SCGB2A2 (mammaglobin 1), and SCGB3A1 (uteroglobin-related protein 2) were studied. The regulation of SCGBs mRNA expression in normal nasal mucosa by proinflammatory, Th1, and Th2 cytokines was studied through nasal explant culture. SCGBs mRNA expression levels in CRSsNP and CRSwNP patients and controls were compared. The mRNA levels were detected by means of quantitative reverse transcriptase-polymerase chain reaction. The protein expression of SCGB3A2 (UGRP1) was analyzed using immunohistochemistry.
The expression of SCGBs except SCGB1D2 (lipophilin B) could be found in upper airway and be differentially regulated by different cytokines. SCGB3A2 (UGRP1) mRNA expression was induced by Th1 cytokine, but suppressed by proinflammatory and Th2 cytokines. SCGBs mRNA expression was altered in CRS; particularly, SCGB3A2 (UGRP1) protein and mRNA expression was markedly decreased in both CRSsNP and CRSwNP and its protein levels inversely correlated with the number of total infiltrating cells, preoperative sinonasal CT scores, and postoperative endoscopy and symptom scores.
SCGBs except SCGB1D2 (lipophilin B) are expressed in human upper airway and their expression can be differentially regulated by inflammatory cytokines. SCGBs mRNA expression is altered in CRS. Reduced production of UGRP1, which is likely due, at least in part, to a local cytokine environment, may contribute to the hyper-inflammation in CRS and correlates with response to surgery.
Secretoglobin (SCGB) superfamily is a group of small, secreted, dimeric proteins [1–5]. Our knowledge of the SCGB superfamily is rapidly expanding with the discovery of many new human genes. At present, nine members of this superfamily have been identified in humans, which includes SCGB1A1 (Clara cell 10-kDa protein, CC10), SCGB1C1 (ligand binding protein RYD5, RYD5), SCGB1D1 (lipophilin A, LIPA), SCGB1D2 (lipophilin B, LIPB), SCGB1D4 (interferon-γ inducible SCGB, IIS), SCGB2A1 (mammaglobin 2, MGB2), SCGB2A2 (mammaglobin 1, MGB1), SCGB3A1 (uteroglobin-related protein 2, UGRP2), and SCGB3A2 (uteroglobin-related protein 1, UGRP1) [1–5]. Although the expression of SCGBs has generally been associated with secretory epithelia, such as in the mammary gland and prostate, there have been only few reports of their expression and regulation in human and rodent airways [1–5].
The pathophysiological functions of SCGBs are poorly understood. Limited studies indicate that some SCGBs are associated with malignancies, such as SCGB2A2 (MGB1), SCGB2A1 (MGB2), and SCGB1D1 (LIPA) [1, 2], and some are involved in immune responses, such as SCGB1A1 (CC10), SCGB1D4 (IIS), SCGB3A1 (UGRP2), and SCGB3A2 (UGRP1) [3–7]. CC10 is a prototypical member of SCGB superfamily with anti-inflammatory and immunomodulatory effects. Previous studies from us and others have implicated the diminished expression of CC10 in the pathogenesis of inflammatory upper and lower airway diseases including chronic rhinosinusitis (CRS) and asthma [5–8]. However, as to other SCGBs, whether they are also involved in airway diseases has been rarely studied.
Among SCGB family members, SCGB3A2 (UGRP1) is particularly interesting. SCGB3A2 (UGRP1) possesses significant amino acid sequence similarity to CC10 (SCGB1A1) [4, 9]. Intranasal administration of recombinant adenovirus expressing SCGB3A2 (UGRP1) suppresses the allergen-induced eosinophilic lung inflammation in a mouse model, indicating that SCGB3A2 (UGRP1) may possess a similar anti-inflammatory function as SCGB1A1 (CC10) . Genetic analysis has demonstrated that a single nucleotide polymorphism (SNP) (G/A) at -112bp of the human SCGB3A2 (UGRP1) gene promoter is associated with an increased risk of asthma in a Japanese population [10, 11]. Nevertheless, the expression and the role of SCGB3A2 (UGRP1) in human airway diseases remain largely unknown.
CRS is a complex and heterogeneous syndrome and typically classified into CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP) [12, 13]. To date, although the etiology and the pathogenesis of CRS remain a matter of vigorous debate, the imbalance between pro- and anti-inflammatory responses is believed to initiate and sustain the inflammation exacerbation in CRS [5, 7, 12, 13]. Therefore, indentifying the factors influencing this imbalance would provide new insights into the pathogenesis of CRS.
The purposes of the present study were: (1) to examine the regulation of SCGBs mRNA expression other than SCGB1A1 (CC10) in human normal nasal mucosa by inflammatory cytokines; (2) to compare the expression levels of SCGBs in normal controls and CRSwNP and CRSsNP patients; and (3) to further study the SCGB3A2 (UGRP1) protein expression and its significance in CRS.
This study was approved by the ethical committee of Tongji Medical College of Huazhong University of Science and Technology and conducted with written informed consent from patients.
1. SCGBs expression regulation in ex vivo cultured normal nasal mucosa study: This study population comprised 34 patients undergoing septal surgery and/or turbinectomy because of nasal obstruction. None had a history of persistent mucopurulent drainage, allergic rhinitis, or sinus disease. Inferior turbinate mucosal samples were used for nasal explant culture .
2. SCGBs expression in CRS study: Twenty patients with CRSsNP and 20 patients with CRSwNP who had bilateral CRS were recruited. The diagnosis of CRSsNP and CRSwNP was made according to the current European EAACI Position Paper on Rhinosinusitis and Nasal Polyps and American guideline [12, 13]. Diseased ethmoid sinus mucosa from the most hypertrophied and hyperemic regions and NP tissues from the apex region of polyps were collected during surgery. As controls, inferior turbinate mucosal samples were taken during surgery from 16 patients undergoing septoplasty and/or turbinectomy because of nasal obstruction and not having any sinus disease or allergic rhinitis. Surgical samples were processed for histology, reverse transcriptase-polymerase chain reaction (RT-PCR), and immunohistochemistry study.
In our study, subjects who had an antrochoanal polyp, cystic fibrosis, fungal sinusitis, or primary ciliary dyskinesia were excluded. None of the patients had an acute upper respiratory infection in the four weeks before the operation. The atopic status was evaluated by skin prick test to a standard panel of aeroallergens. The diagnosis of asthma and aspirin sensitivity was based on history and physician diagnosis. Oral glucocorticoid and intranasal steroid sprays were discontinued at least 3 months and 1 month before surgery, respectively. None had received antileukotrienes and immunotherapy. All patients and controls were Han Chinese from central China.
Clinical data of patients enrolled in SCGBs expression regulation study and SCGBs expression in CRS study
SCGBs expression in CRS study
SCGBs expression regulation study
Sex, male, n (%)
Age (years), mean ± SD
30.7 ± 11.4
35.5 ± 11.0
34.4 ± 12.7
31.7 ± 12.0
Patients with asthma, n (%)
Patients with positive skin prick test results, n (%)
Patients with aspirin sensitivity, n (%)
Assessment of CRS clinical severity
For CRS patients, preoperative coronal CT scans through paranasal sinuses were obtained and scored using the Lund-Mackay system, as previously described . Symptom evaluation and endoscopic examination were taken before and 12 months after the surgery. A symptom questionnaire based on a visual analog score (VAS) of 0 to 10 according to severity was used. A total VAS score was calculated based on the sum of five VAS symptom domains, including nasal blockage, headache, facial pain, alteration of sense of smell, and nasal discharge . In addition, patients were asked to rate his/her overall burden of CRS symptoms . Endoscopy physical findings were scored according to Lanza and Kennedy .
Nasal explant culture
Normal inferior turbinate mucosal tissues were obtained during surgery and immediately cut into multiple fragments of approximately 6 mm3. One was processed for histologic evaluation and others were used for tissue culture. Sections of tissue were placed on 0.4 mm-well inserts (Millipore Corp., Billerica, MA, USA) in 2 mL of Dulbecco's modified Eagle's medium/F-12 supplemented with 2 mM L-glutamine, 100 U/mL penicillin, and 100 mg/mL streptomycin (Invitrogen, Grand Island, NY, USA). The tissue was oriented with the epithelium being exposed to the air, forming an air-liquid interface to mimic the in vivo situation [6, 16, 17]. For dose response experiments, the tissues were incubated in the presence of TNF-α (1, 10, and 100 ng/ml), IL-1β (1, 10, and 100 ng/ml), INF-γ (0.1, 1, and 10 ng/ml), IL-4 (1, 10, and 100 ng/ml), or IL-13 (1, 10, and 100 ng/ml) for 12 h. These cytokines were purchased from R&D Systems (Minneapolis, MN, USA). For time course experiments, the tissues were incubated with TNF-α (20 ng/ml), IL-1β (20 ng/ml), IL-4 (20 ng/ml), IL-13 (20 ng/ml), or INF-γ (1 ng/ml) for various time durations between 4 and 24 h. The tissues were cultured at 37˚C with 5% CO2 in humidified air.
Primers used for quantitative PCR analysis of SCGB genes expression
Annealing temperature (˚C)
reverse, 5'- CATAGGCCATCGTATCCACGC-3'
forward, 5'- CGGAATTCCCCCGCGCCATGAAGCTC-3'
reverse, 5'- ACATCTAGAGCCAAACACTGTCAGG-3'.
Routine staining, SCGB3A2 (UGRP1) immunohistochemistry, and quantification
Paraffin sections (4 μm) were stained with hematoxylin and eosin. The number of inflammatory cells per high-power filed (HP) was determined by counting 10 randomly selected fields in a blinded fashion at 400 × magnification by 2 independent physician who were blind to the clinical data. The difference in counting results between 2 independent investigators was less than 10%. In case of disagreement (the two counts differed by > 10%), a consensus was reached by reviewing the specimen at a multihead microscope by our research team.
As to immunohistochemical staining of SCGB3A2 (UGRP1) protein, the sections were stained with goat anti-SCGB3A2 (UGRP1) antibody (1:100; R&D Systems). SCGB3A2 (UGRP1) was detected using the streptavidin-peroxidase complex method with a histostain-plus kit (Zhongshan Golden Bridge Biotechnology, Beijing, China) as previously described . Color development was achieved with 3', 3'-diaminobenzidine, which rendered positive cells brown. A species-matched antibody was used as a negative control. Quantitative measurement of SCGB3A2 (UGRP1) protein expression was analyzed using the HPIAS-1000 automated image analysis system as described elsewhere . Ten microscopic fields were randomly selected from each slide under × 400 magnification. Results were presented as 1/gray scores, which positively correlate with the intensity of immunoreactivity .
Results are presented as mean ± SD, or in box-and-whisker plots. Paired sets of data were compared with Mann-Whitney U-test. The Spearman test was used to determine correlations. Paired t-test was used in tissue culture data analysis. Data analyses were performed by using SPSS for Windows (SPSS Inc., Chicago, IL, USA). The level of significance was considered at a P value of less than 0.05.
The cytokine-driven regulation of SCGBs mRNA expression in normal nasal mucosa
The mRNA expression of SCGBs in sinonasal mucosa from controls and CRS patients
SCGB3A2 (UGRP1) protein expression and its correlation with inflammatory cells infiltration and clinical features in CRS
Disease severity assessment
8.40 ± 4.21
14.90 ± 5.69
4.55 ± 1.90
7.05 ± 2.04
Overall VAS scores
6.15 ± 1.39
7.15 ± 1.48
Total VAS scores
23.35 ± 5.09
23.90 ± 4.78
1.61 ± 1.33
3.05 ± 2.22
Overall VAS scores
2.33 ± 2.28
3.11 ± 1.73
Total VAS scores
5.72 ± 5.44
7.68 ± 6.29
In the present study, extending our previous finding of SCGB1A1 (CC10) [5, 6], we demonstrated the cytokine-driven expression regulation of SCGB superfamily members in human upper airways and their overall expression profile in CRS for the first time. We detected the mRNA expression of all SCGBs except SCGB1D2 (LIPB) in sinonasal mucosa. The expression of SCGB1D2 (LIPB) is also absent in normal lung tissues , suggesting that this SCGB may be not important for airway functions. We confirmed the mRNA expression of SCGB2A1 (MGB2) in nasal mucosa, which has been demonstrated by previous gene array studies [6, 18]. Our unpublished data indicate that SCGB2A1 (MGB2) is expressed by submucosal glands in sinonasal mucosa. Previous investigations have also indentified some of different SCGBs in other parts of the human respiratory tract, such as SCGB3A2 (UGRP1) and SCGB3A1 (UGRP2) in the epithelium of lung, and SCGB2A2 (MGB1) in trachea [1, 19, 20]. Our current study demonstrated that in sinonasal mucosa SCGB3A2 (UGRP1) was also mainly produced by epithelial cells. By contrast, SCGB1C1 (RYD5) and SCGB1D4 (IIS) have, to the present author's knowledge, not been demonstrated in human respiratory airway mucosa until now, although SCGB1C1 (RYD5) and SCGB1D4 (IIS) have been detected in Bowman's glands of rat olfactory mucosa and human lymphoid tissues and cells, respectively [3, 21]. The cellular locations of SCGB1C1 (RYD5) and SCGB1D4 (IIS) in sinonasal mucosa are unclear. Due to the lack of commercially available antibodies, further in situ hybridization study may be helpful in clarifying their cellular locations. The expression regulation of SCGBs has rarely been studied. In airway inflammation, proinflammatory, and Th1 and Th2 relevant cytokines play a crucial role. The increased expression of IL-1β, TNF-α, INF-γ, and IL-4 has been demonstrated in CRS, which may be involved in the inflammation perpetuation and exaggeration . Therefore, in this study, SCGBs expression regulation by these cytokines was studied in nasal mucosa. Limited studies have indicated that IL-4 and IL-13 can induce, whereas INF-γ can inhibit the expression of SCGB3A1 (UGRP2) in a mouse transformed Clara cell line ; IL-5 may suppress SCGB3A2 (UGRP1) expression in murine lung tissues in vivo ; and INF-γ can up-regulate SCGB1D4 (IIS) expression in human lymphoblast cells . In the present study, we found that SCGBs expression in human nasal mucosa could be differentially modulated by various inflammatory cytokines. On the other hand, the same cytokine could evoke distinct responses of different SCGB genes. Our results suggest that the expression of SCGBs is finely controlled by local immune responses in airways and SCGBs may be involved in cytokine-induced airway inflammation.
In present study, we found altered expression profiles of SCGBs in CRS. Since the biological functions of SCGBs are poorly understood, their roles in CRS mostly remain speculative. The unique increase of SCGB1C1 (RYD5) and decrease of SCGB3A1 (UGRP2) in CRSwNP, but not in CRSsNP, suggest that these two SCGBs may be more particularly involved in the polyp formation. Choi et al found that SCGB1D4 (IIS) can modulate lymphoblast cell migration ; therefore, the enhanced expression of SCGB1D4 (IIS) in both CRSsNP and CRSwNP may contribute to the persistent immune responses in CRS. The expression of SCGB1D1 (LIPA), SCGB2A1 (MGB2), and SCGB2A2 (MGB1) has been shown to be upregulated in human lung cancers [1, 2]. In the current study, we found that SCGB2A2 (MGB1) expression was upregulated, whereas SCGB2A1 (MGB2) expression was down-regulated in both CRSsNP and CRSwNP, which is consistent with our previous gene array data . In addition, we found that SCGB1D1 (LIPA) expression was up-regulated in CRSsNP. The aberrant expression of these three SCGBs suggests that they may be related to epithelial proliferation and tissue hyperplasia in CRS. However, obviously, further studies are needed to test these hypotheses and to elucidate the roles of SCGBs in CRS.
Among SCGBs, SCGB3A2 (UGRP1) is particularly interesting, given its structure and function similarities with SCGB1A1 (CC10) [4, 9]. SCGB3A2 (UGRP1) is highly specific for airways [4, 9]. Although the decreased expression and an anti-inflammatory role of SCGB3A2 (UGRP1) in allergic airway inflammation was observed in an animal model [4, 9], its involvement in human airway diseases is largely unknown. In this study, we found that the mRNA and protein expression of SCGB3A2 (UGRP1) was dramatically down-regulated in both CRSsNP and CRSwNP, and SCGB3A2 (UGRP1) was mainly produced by epithelial cells in sinonasal mucosa, which is similar to the expression pattern of SCGB1A1 (CC10) [5–7]. Contrast to our findings, Burbure et al found that SCGB3A2 (UGRP1) levels in sputum were increased in patients with asthma and rhinitis . However, they did not examine the SCGB3A2 (UGRP1) expression in local mucosa and the protein levels in sputum may not correlate with the expression intensity in local mucosa. As shown in our current study, SCGB3A2 (UGRP1) expression could be modulated by proinflammatory, Th1 and Th2 cytokines in nasal mucosa; therefore, the decreased expression of SCGB3A2 (UGRP1) in CRS might relate to the specific local cytokine environment in CRS [5, 25]. More importantly, we found significant negative correlations between SCGB3A2 (UGRP1) expression and total inflammatory cells infiltration and disease severity evaluated by CT scan. In the light of the potential anti-inflammatory function of SCGB3A2 (UGRP1) indicated by animal experiments, our results suggest that the loss of SCGB3A2 (UGRP1) expression may contribute to the hyper-inflammation in CRS. However, this needs to be validated by function studies in human subjects in future. Furthermore, we found that SCGB3A2 (UGRP1) levels negatively correlated with post-operative symptom and endoscopy scores. This would be of considerable clinical value. Since detecting of potential responders among candidates for surgical treatment by certain biomarkers remains a difficult task . This finding not only suggests that SCGB3A2 (UGRP1) may be a predictor of surgical response but also strengthens the involvement of SCGB3A2 (UGRP1) in the pathogenesis of CRS.
In this study, inferior turbinates were used as control, because it is difficult to obtain enough normal ethmoid mucosa samples due to ethical consideration. It is known that sinus and turbinate mucosa are both covered by the respiratory epithelium and share a number of similarities in histology and expression profiles of many common and important immune and biological molecules. Although we are not able to rule out the possibility that the differences observed between controls and CRS might be influenced by comparing these different tissue localizations, one could see clear differences between ethmoid tissue obtained from CRSsNP and CRSwNP patients.
In conclusion, this study, for the first time, shows the expression features of SCGB superfamily members in CRS and their cytokine-driven regulation in upper airways. Our results suggest the reduced production of SCGB3A2 (UGRP1), which is likely due, at least in part, to a local inflammatory environment, may contribute to the hyperinflammation in CRS and correlates with response to surgery.
Grant Support: This study was supported by the National Nature Science Foundation of China (NSFC) grants 30872847 and 81020108018, and the program for New Century Excellent Talents in University from the State Education Ministry (NCET-07-0326) to ZL, and NSFC grant 30901660 to XL.
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