- Open Access
Smoking-mediated up-regulation of GAD67 expression in the human airway epithelium
© The Author(s) 2010
Received: 18 December 2009
Accepted: 29 October 2010
Published: 29 October 2010
The production of gamma-amino butyric acid (GABA) is dependent on glutamate decarboxylases (GAD65 and GAD67), the enzymes that catalyze the decarboxylation of glutamate to GABA. Based on studies suggesting a role of the airway epithelial GABAergic system in asthma-related mucus overproduction, we hypothesized that cigarette smoking, another disorder associated with increased mucus production, may modulate GABAergic system-related gene expression levels in the airway epithelium.
We assessed expression of the GABAergic system in human airway epithelium obtained using bronchoscopy to sample the epithelium and microarrays to evaluate gene expression. RT-PCR was used to confirm gene expression of GABAergic system gene in large and small airway epithelium from heathy nonsmokers and healthy smokers. The differences in the GABAergic system gene was further confirmed by TaqMan, immunohistochemistry and Western analysis.
The data demonstrate there is a complete GABAergic system expressed in the large and small human airway epithelium, including glutamate decarboxylase, GABA receptors, transporters and catabolism enzymes. Interestingly, of the entire GABAergic system, smoking modified only the expression of GAD67, with marked up-regulation of GAD67 gene expression in both large (4.1-fold increase, p < 0.01) and small airway epithelium of healthy smokers (6.3-fold increase, p < 0.01). At the protein level, Western analysis confirmed the increased expression of GAD67 in airway epithelium of healthy smokers compared to healthy nonsmokers (p < 0.05). There was a significant positive correlation between GAD67 and MUC5AC gene expression in both large and small airway epithelium (p < 0.01), implying a link between GAD67 and mucin overproduction in association with smoking.
In the context that GAD67 is the rate limiting enzyme in GABA synthesis, the correlation of GAD67 gene expression with MUC5AC expressions suggests that the up-regulation of airway epithelium expression of GAD67 may contribute to the increase in mucus production observed in association with cigarette smoking.
Gamma-aminobutyric acid (GABA) is a multifunctional mediator that functions as a neurotransmitter in the central nervous system and a trophic factor during nervous system development, affecting proliferation, differentiation and cell death [1–3]. GABA is synthesized from glutamate, and catalyzed by GAD65 and GAD67, glutamic acid decarboxylase [1–3]. In the CNS, transporters, receptors and catabolic enzymes work in a coordinated fashion to control the availability of GABA [1–3]. It is now recognized that GABA also functions in a variety of organs outside of the CNS [1, 3, 4]. In the lung, a series of recent studies suggest that the GABAergic signaling system plays a role in the control of asthma-related airway constriction and mucin secretion [5–9].
In the context that goblet cell hyperplasia and mucin overproduction is also associated with cigarette smoking [10–12], we hypothesized that components of the GABAergic system may also be altered in the airway epithelium of cigarette smokers. To assess this hypothesis, we examined our microarray database of large and small airway gene expression of healthy nonsmokers and healthy smokers to determine if the GABAergic system was expressed. This was verified by PCR analysis. The data demonstrate there is expression of genes for a complete GABAergic system in the airway epithelium. Interestingly, the expression of GAD67 was markedly modified by smoking, with increased expression in healthy smokers compared to healthy nonsmokers at the mRNA and protein levels. In the context that mucus overproduction is commonly associated with cigarette smoking, GAD67 may be a pharmacologic target for the treatment of smoking-related disorders.
Healthy nonsmokers and healthy smokers were recruited using local print media. The study population was evaluated at the Department of Genetic Medicine Clinical Research Facility under the auspices of the Weill Cornell NIH Clinical and Translational Science Center with approval by the Weill Cornell Medical College Institutional Review Board. Written informed consent was obtained from each volunteer before enrollment in the study. Individuals were determined to be phenotypically normal on the basis of clinical history and physical examination, routine blood screening tests, urinalysis, chest X-ray, ECG and pulmonary function testing. Current smoking status was confirmed by history, venous carboxyhemoglobin levels and urinalysis for levels of nicotine and its derivative cotinine. All individuals were asked not to smoke for at least 12 hr prior to bronchoscopy.
Collection of Airway Epithelial Cells
Epithelial cells from the large and small airways were collected using flexible bronchoscopy. After achieving mild sedation and anesthesia of the vocal cords, a flexible bronchoscope (Pentax, EB-1530T3) was advanced to the desired bronchus. Large airway epithelial samples were collected by gentle brushing of the 3rd to 4th order bronchi and small airway samples were collected from 10th to 12th order bronchi using methods previously described . The large and small airway epithelial cells were subsequently collected separately in 5 ml of LHC8 medium (GIBO, Grand Island, NY). An aliquot of this was used for cytology and differential cell count and the remainder was processed immediately for RNA extraction. Total cell counts were obtained using a hemocytometer, whereas differential cell counts were determined on sedimented cells prepared by centrifugation (Cytospin 11, Shandon Instruments, Pittsburgh, PA) and stained with DiffQuik (Baxter Healthcare, Miami, FL).
RNA Extraction and Microarray Processing
The HG-U133 Plus 2.0 microarray (Affymetrix, Santa Clara, CA), which includes probes for more than 47,000 transcripts genome-wide, was used to evaluate gene expression. Total RNA was extracted using a modified version of the TRIzol method (Invitrogen, Carlsbad, CA), in which RNA is purified directly from the aqueous phase (RNeasy MinElute RNA purification kit, Qiagen, Valencia, CA). RNA samples were stored in RNA Secure (Ambion, Austin, TX) at -80°C. RNA integrity was determined by running an aliquot of each RNA sample on an Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA). The concentration was determined using a NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE). Double-stranded cDNA was synthesized from 1 to 2 μg total RNA using the GeneChip One-Cycle cDNA Synthesis Kit, followed by cleanup with GeneChip Sample Cleanup Module, in vitro transcription (IVT) reaction using the GeneChip IVT Labeling Kit, and cleanup and quantification of the biotin-labeled cDNA yield by spectrophotometry. All kits were from Affymetrix (Santa Clara, CA). All HG-U133 Plus 2.0 microarrays were processed according to Affymetrix protocols, hardware and software, including being processed by the Affymetrix fluidics station 450 and hybridization oven 640, and scanned with an Affymetrix Gene Array Scanner 3000 7G. Overall microarray quality was verified by the following criteria: (1) RNA Integrity Number (RIN) ≥7.0; (2) 3'/5' ratio for GAPDH ≤3; and (3) scaling factor ≤10.0.
Microarray Data Analysis
Captured images were analyzed using Microarray Suite version 5.0 (MAS 5.0) algorithm (Affymetrix) as previously described [13–15]. The data were normalized using GeneSpring version 7.0 software (Agilent Technologies, Palo Alto, CA) as follows: (1) per array, by dividing raw data by the 50th percentile of all measurements; and (2) per gene, by dividing the raw data by the median expression level for all the genes across all arrays in a dataset.
To confirm the expression of the genes in the GABAergic system, total RNA from large airway epithelium and small airway epithelium was prepared as described above. Total RNA from whole human brain (Clontech, Mountain View, CA) was used as a positive control. RNA was reverse transcribed by TaqMan Reverse Transcription Regents (ABI, Foster City, CA). Routine PCR was performed using Platinum PCR Supermix (Invitrogen, Carlsbad, CA) at indicated temperatures and times (Additional file 1, Table S1).
TaqMan RT-PCR Confirmation of Microarray Expression Levels
To quantify relative mRNA levels of GAD67, TaqMan real-time RT-PCR was performed on a random sample of large and small airway samples of 10 healthy nonsmokers and 12 healthy smokers that had been used for the HG-U133 Plus 2.0 microarray analyses. First, cDNA was synthesized from 2 μg RNA in a 100 μl reaction volume, using the Reverse Transcriptase Reaction Kit (Applied Biosystems), with random hexamers as primers. Dilutions of 1:10 and 1:100 were made from each sample and triplicate wells were run for each dilution. TaqMan PCR reactions were carried out using pre-made kits from Applied Biosystems and 2 μl of cDNA was used in each 25 μl reaction volume. β-actin was used as the endogenous control, and relative expression levels were determined using the ΔΔCt method (Applied Biosystems). The β-actin probe was labeled with VIC and the probe for GAD67 with FAM. The PCR reactions were run in an Applied Biosystems Sequence Detection System 7500.
Localization of GAD67 Expression in Human Airway Epithelium
To determine the airway epithelial localization of GAD67 expression, bronchial biopsies were obtained by flexible bronchoscopy from the large airway epithelium of 10 healthy nonsmokers and 10 healthy smokers . Immunohistochemistry was carried out on these paraffin-embedded endobronchial biopsies. Sections were deparaffinized and rehydrated through a series of xylenes and alcohol. To enhance staining, an antigen retrieval step was carried out by boiling the sections at 100°C, 20 min in citrate buffer solution (Labvision, Fremont, CA), followed by cooling at 23°C, 20 min. Endogenous peroxidase activity was quenched using 0.3% H2O2, and blocking was performed with normal goat serum to reduce background staining. Samples were incubated with the mouse monoclonal anti-GAD67 antibody (1 μg/μl at 1/25 dilution, Millipore, Billerica, MA), 16 hr, 4°C. Cytospin slides of 293 cells transfected with pcDNA3.1-GAD67, and pcDNA3.1 plasmids were used as controls. Vectastain Elite ABC kit (Vector Laboratories, Burlingame, CA) and 3-amino-9-ethylcarbazole (AEC) substrate kit (Dako, Carpinteria, CA) were used to detect antibody binding, and the sections were counterstained with hematoxylin (Sigma-Aldrich, St. Louis, MO), and mounted using GVA mounting medium (Zymed, San Francisco, CA). Brightfield microscopy was performed using a Nikon Microphot microscope and images were captured with an Olympus DP70 CCD camera.
Western analysis was used to quantitatively assess GAD67 protein expression in small airway epithelium from healthy nonsmokers and healthy smokers. Brushed small airway epithelial cells were obtained as described above. Initially, the cells were centrifuged at 600 g, 5 min, 4°C. The whole cells were lysed with red cell lysis buffer (Sigma-Aldrich), followed by whole cell lysis buffer (ACK lysing buffer, Invitrogen), and then protease inhibitor (Cell Lytic Mammalian Tissue Lysis/Extraction reagent, Sigma-Aldrich) was added to the sample. The sample was centrifuged at 10,000 g and the protein-containing supernatant was collected. The protein concentrations were assessed using a bicinchoninic acid (BCA) protein concentration kit (Pierce, Rockford, IL). Equal concentration of protein (20 μg), mixed with SDS Sample Loading Buffer (Bio-Rad, Hercules, CA) and reducing agent, was loaded on Tris-glycine gels (Bio-Rad). Protein electrophoresis was carried out at 100 V, 2 hr, 23°C. Sample proteins were transferred (25 V, 1 hr, 4°C) to a 0.45 μm PVDF membrane (Invitrogen) using Tris-glycine transfer buffer (Bio-Rad). After transfer the membranes were blocked with 5% milk in PBS for 1 hr, 23°C. The membranes were incubated with primary mouse monoclonal anti-GAD67 antibody (Millipore, Billerica, MA) at 1:2000 dilution, 2 hr, 4°C. Protein extracted from pcDNA 3.1-GAD67 transfected 293 cells was used as a positive control. Detection was performed using horseradish peroxidase-conjugated anti-mouse antibody (1:10,000 dilution, Santa Cruz Biotechnology, Santa Cruz, CA) and the Enhanced Chemiluminescent reagent (ECL) system (GE, Healthcare, Pittsburgh, PA) using Hyperfilm ECL (GE Healthcare). The membrane was subsequently stripped and reincubated with horseradish peroxidase-conjugated anti-β-actin antibody (Santa Cruz Biotechnology) as a control for equal protein concentration. To assess the Western analyses quantitatively, the film was digitally imaged, maintaining exposure within the linear range of detection. The contrast was inverted, the pixel intensity of each band determined, and the background pixel intensity for a negative area of the film of identical size subtracted using MetaMorph image analysis software (Universal Imaging, Downingtown, PA).
For MUC5AC staining in large airway and small airway epithelium, brush cells cytospin slides were stained with mouse anti-human MUC5AC antibody (Vector, Burlingame, CA) and detected by Cy3 labeled goat anti-mouse antibody (Jackson, West Grove, PA). Nuclei were counterstained with DAPI (Invitrogen, Carlsbad, CA). Based on the microarray data, we defined "high GAD67" or "high MUC5AC" gene expression as ≥median + 1 standard deviation and low GAD67 or low MUC5AC gene expression as ≤median - 1 standard deviation. Based on this criteria, 3 healthy smokers with high GAD67 and high MUC5AC gene expression and 3 healthy smokers with low GAD67 and low MUC5AC gene expression were assessed for MUC5AC protein expression by immunofluorescence staining.
HG-U133 Plus 2.0 microarrays were analyzed using GeneSpring software. Average expression values for GAD67 in large and small airway samples (HG-U133 Plus 2.0) were calculated from normalized expression levels for nonsmokers and healthy smokers. Statistical comparisons for microarray data were calculated using GeneSpring software and associated two-tailed Students t-test. Benjamini-Hochberg correction was applied to limit the false discovery rate. Statistical comparisons for categorical data were achieved using Chi-squared test. Correlations were performed using Pearson correlation. All other statistical comparisons were calculated using a two-tailed (Welsh) t-test.
Web Deposition of Data
All data has been deposited in the Gene Expression Omnibus (GEO) site (http://www.ncbi.nlm.nih.gov/geo), curated by the National Center for Bioinformatics. Accession number for the data is GSE17905.
Study Population of Airway Epithelial Samples 1
41 ± 8
44 ± 7
42 ± 11
43 ± 7
Smoking history (pack-yr)
28 ± 17
Urine nicotine (ng/ml)
746 ± 904
Urine cotinine (ng/ml)
973 ± 690
1246 ± 974
0.64 ± 0.93
0.4 ± 0.8
1.8 ± 1.9
106 ± 13
110 ± 11
107 ± 14
109 ± 13
107 ± 17
110 ± 12
106 ± 15
107 ± 14
82 ± 5
81 ± 5
82 ± 6
80 ± 5
100 ± 14
103 ± 11
101 ± 16
95 ± 11
99 ± 15
94 ± 11
Total number × 106
7.0 ± 3
7.0 ± 3.3
6.3 ± 2.9
7.2 ± 3.0
99.7 ± 0.6
99.8 ± 0.5
99.3 ± 1.1
99.1 ± 1.3
0.3 ± 0.6
0.2 ± 0.5
0.7 ± 1.1
0.8 ± 1.3
Differential cell count (%)
53.6 ± 6.6
47.8 ± 13.7
74.3 ± 7.4
65.7 ± 12.5
10 ± 4.4
10 ± 4.1
6.6 ± 3.5
9.1 ± 4.5
22.4 ± 3.4
25.9 ± 9.9
11.1 ± 5.3
12.7 ± 6.7
14.1 ± 5.2
16.5 ± 8.9
7.3 ± 3.2
11.8 ± 6.7
Sampling of Airway Epithelium
Airway epithelial cells were obtained by fiberoptic bronchoscopy and brushing of the large (3rd to 4th order) and small (10th to 12th order) airways. The number of cells recovered ranged from 6.3 to 7.2 × 106 (Table 1). The percent epithelial cells recovered was, on average, 99% in all groups. The various categories of airway epithelial cells were, as expected, from the large and small airways [13, 15].
Expression of GABAergic System-related Genes in the Airway Epithelium
Expression of GABAergic System Genes in Large Airway and Small Airway Epithelium of Healthy Smokers Compared to Healthy Nonsmokers1
Small airway (smoker/nonsmoker)2
Probe set ID
p value 3
P call (%) 4
p value 3
P call (%) 4
glutamate decarboxylase 2
glutamate decarboxylase 1
2.07 × 10-5
2.33 × 10-11
gamma-aminobutyric acid (GABA) A receptor, alpha 1
gamma-aminobutyric acid (GABA) A receptor, alpha 2
gamma-aminobutyric acid (GABA) A receptor, alpha 3
gamma-aminobutyric acid (GABA) A receptor, alpha 4
gamma-aminobutyric acid (GABA) A receptor, alpha 5
gamma-aminobutyric acid (GABA) A receptor, alpha 6
gamma-aminobutyric acid (GABA) A receptor, beta 1
gamma-aminobutyric acid (GABA) A receptor, beta 2
gamma-aminobutyric acid (GABA) A receptor, beta 3
gamma-aminobutyric acid (GABA) A receptor, gamma 1
gamma-aminobutyric acid (GABA) A receptor, gamma 2
gamma-aminobutyric acid (GABA) A receptor, gamma 3
gamma-aminobutyric acid (GABA) A receptor, epsilon
gamma-aminobutyric acid (GABA) receptor, theta
gamma-aminobutyric acid (GABA) A receptor, delta
gamma-aminobutyric acid (GABA) A receptor, pi
gamma-aminobutyric acid (GABA) receptor, rho 1
gamma-aminobutyric acid (GABA) receptor, rho 2
gamma-aminobutyric acid (GABA) receptor, rho 3
gamma-aminobutyric acid (GABA) B receptor, 1
1.79 × 10-4
gamma-aminobutyric acid (GABA) B receptor, 2
solute carrier family 6 (neurotransmitter transporter, GABA), member 1
solute carrier family 6 (neurotransmitter transporter, GABA), member 13
solute carrier family 6 (neurotransmitter transporter, GABA), member 11
solute carrier family 6 (neurotransmitter transporter, betaine/GABA), member 12
solute carrier family 32 (GABA vesicular transporter), member 1
7.25 × 10-2
5.41 × 10-3
aldehyde dehydrogenase 5 family, member A1
Independent of smoking status, the only GABA synthesis enzymes expressed in the large airway epithelium and small airway epithelium was GAD67. In regard to transporters, there was no GAT-3 and VGAT expression in human large and small airway epithelium. For the GABA metabolism-related genes, both GABAT and ALDH5A1 were expressed in the large and small airway epithelium. In summary, each functional group of the GABA system has genes expressed in airway epithelium, forming a complete GABAergic system. RT-PCR confirmed that a complete GABAergic system was expressed in the airway epithelium (Figure 2C).
Up-regulation of GAD67 in Large and Small Airway Epithelium of Healthy Smokers
Immunohistochemical Assessment of GAD67 Expression
Western Analysis of GAD67 Protein Expression
Association Between GAD67 and MUC5AC Gene Expression in Smokers
Cigarette smoking is associated with mucus hypersecretion by the airway epithelium [10–12]. While the control of mucus secretion is complex, a role of the GABAergic system has been suggested to mediate, in part, the hypersecretion of mucus associated with asthma [6–9, 17]. In the context that cigarette smoking is also associated with mucus hypersecretion, in the present study we asked the question: Does smoking alter the gene expression pattern of GABAergic system genes in the respiratory epithelium? Assessment of our database of airway epithelial gene expression generated by microarrays showed that, while many of the GABAergic system genes are expressed in the human large and small airway epithelium, cigarette smoking is associated with changes in gene expression only of GAD67, a gene controlling the synthesis of GABA . A striking increase in gene expression levels of GAD67 was observed in the large and small airway epithelium of healthy smokers compared to healthy nonsmokers, a finding confirmed at the mRNA level by TaqMan PCR; and at the protein level qualitatively by immunohistochemistry, and quantitatively by Western analysis. There was a positive correlation between GAD67 gene expression and MUC5AC at the mRNA level in both small and large airway epithelium, as well as by MUC5AC staining, suggesting a link between mucus overproduction and GAD67 overexpression in association with smoking.
GABA is the major inhibitory neurotransmitter in the mammalian central nervous system [2, 3]. In the mammalian brain, GABA is synthesized primarily from glutamate in a reaction that is catalyzed by 2 glutamic acid decarboxylase enzymes, GAD65 and GAD67, coded by different genes [1–3]. GABA is then loaded into synaptic vesicles by a vesicular neurotransmitter transporter (VGAT) and liberated from nerve terminals by calcium-dependent exocytosis. Nonvesicular forms of GABA secretion (e.g., by reverse transporter action) have also been described and are likely important during development . After being released from presynaptic nerve terminals, GABA exerts its physiological effects through ionotropic GABA-A receptors and metabotropic GABA-B receptors . The GABAergic neurotransmission is terminated by rapid uptake of the neurotransmitter from the synaptic cleft into neurons and glial cells by specific high-affinity GABA transporters . There are 4 distinct genes encoding membrane GABA transporters, GAT-1, GAT-2, GAT-3, and BGT-1 . Subsequently, GABA is metabolized by a transamination reaction that is catalyzed by GABA transaminase (GABA-T). Succinic semialdehyde dehydrogenase (ALDH5A1), which helps entry of the GABA carbon skeleton into the tricarboxylic acid cycle, is the final enzyme of GABA catabolism . GABAergic system genes are present not only in the brain, but also in other organs, including liver, kidney, pancreas, testis, oviduct, adrenal, and lung [3, 4].
GABAergic System in the Lung
In the lung, immunohistochemistry studies of the guinea pig trachea has identified GABA in airway epithelium, chondrocytes and connective tissue near smooth muscle . GAD65/67 mRNA has been detected in human and mouse airway epithelium at the mRNA level by RT-PCR and at the protein level by Western analysis and immunohistochemistry [7, 22]. GABA and GAD 65/67 are also expressed in mouse pulmonary neuroendocrine cells . Of the 19 GABA-A receptor subunits identified in the mammalian genome, subunits alpha1, pi and delta have been detected in human airway epithelium by Western analysis, subunits beta 2/beta 3 in mouse airway epithelium by immunohistochemistry, and alpha 2, gamma 3, beta 1 and pi in rat airway epithelium by immunohistochemistry . Some GABA-A receptor subunits have also been identified in alveolar epithelial cells . There are different expression patterns of some of the GABA-A receptor subunits during rat lung development . Of the GABA-B receptors, both GABBR1 and GABBR2 subunits mRNA have been detected in human airway epithelium and both subunits have been identified by Western analysis and immunohistochemistry in guinea pig trachea . Using specific agonists, GABA-B receptors coupling to G proteins in general and its specific coupling to the G protein was shown in a human airway epithelial cell line . To our knowledge, there has been no prior assessment of expression of GABA transporters or of GABA catabolism enzymes in the human airway epithelium.
In the present study, we categorized the expression of GABAergic system genes into 4 groups based on their GABA-related function: synthesis, receptor, transport and metabolism. The analysis demonstrated a complete GABAergic system exists in the human large and small airway epithelium, although there are differences compared to the central nervous system. Interestingly, in the human airway epithelium there is no VGAT expression, suggesting GABA is released from airway epithelial cells in a vesicle independent fashion . Consistent with our data, high pressure liquid chromatography demonstrated that GABA could be produced in the guinea pig trachea epithelium , and a functional GABA transporter has been demonstrated in cultured human airway epithelial cells .
Modification of GAD67 Expression by Smoking
Recent studies suggest the GABAergic system may have a role in oxidative stress protection in neuron-related cells and airway mucus production [7, 28, 29]. Our data demonstrate that, while many of the GABAergic system genes are expressed in the human large and small airway epithelium, only GAD67 is modified by cigarette smoking, with a marked increase in gene expression levels of GAD67 in the large and small airway epithelium of healthy smokers compared with healthy nonsmokers, and with a positive correlation between GAD67 and MUC5AC, the major airway mucus-related gene . Considering the important role of ion channels in airway surface water balance [30, 31], further studies could be directed to explore the effect of GABAergic system changes affected by smoking on the liquid microenvironment of airway epithelium.
The mechanisms responsible for GAD67 gene expression up-regulation by cigarette smoking remain to be elucidated. It is known that nicotine, by activating nicotinic acetylcholine receptors located on cortical or hippocampal GABAergic interneurons, can up-regulate GAD67 expression via an epigenetic mechanism . Inhibitors of DNA methyltransferases and histone deactylases induce GAD67 expression [33, 34]. In contrast to this observation, nicotine suppresses protein levels of GAD isozymes (mainly GAD65) and GABA in pancreatic ductal adenocarcinoma tissue . Interestingly, nuclear factor-kappa B activation through oxidative stress can up-regulate GAD67 expression , and the early growth response factor 1-related pathway also mediates GAD67 up-regulation . Glucocorticoid hormones can modulate GAD expression by transcriptional activation of the GAD67 promoter . Finally, GAD can also be regulated at the post-translational level by protein phosphorylation, palmitoylation and cleavage . Together, these findings suggest that cigarette smoking may have a complicated effect on GAD activity.
GABAergic System and Mucus Overproduction
A variety of observations link the GABAergic system to mucus overproduction. Studies by Xiang et al  demonstrated that GABA promotes the proliferation of airway epithelial cells, an effect that was suppressed by a GABA-A receptor antagonist, whereas activation of GABA-A receptors depolarized airway epithelial cells. After exposure to GABA for 6 days, cultured human airway epithelium demonstrated more mucus staining. Moreover, ovalbumin-induced airway goblet cell hyperplasia and mucus overproduction could be blocked with a GABA-A receptor antagonist in vivo. Studies from the same group also showed that IL-4Rα is required for allergen-induced up-regulation of GABAergic system in airway epithelium, which might have a role in goblet cell metaplasia following acute house dust mite exposure .
Fu et al  showed that incubation of rhesus macaque bronchial epithelial cells with nicotine for 48 hr significantly increased mucin mRNA levels. Interestingly, the effect of nicotine was blocked both by the nicotinic antagonists and by the GABA-A receptor antagonists. This suggests that the sequential activation of nicotinic signaling followed by GABAergic signaling is necessary for nicotine to stimulate bronchial epithelial mucus production, and that nicotine-induced mucin overproduction is, in part, dependent on GABA-A receptor signaling in bronchial epithelial cells. Ly6/neurotoxin 1 (Lynx1), the founding member of a family of mammalian prototoxins, modulates nicotinic acetylcholine receptors in vitro by altering agonist sensitivity and desensitization kinetics . Results from Lynx1 knockdown experiments suggested that Lynx1 acts as a negative modulator of nicotine-mediated activation of GABAergic signaling . Interestingly, when BALB/c mice were exposed to secondhand smoke, there was an excellent correlation between increased GABA-A receptor staining and lung mucous cell metaplasia .
Based on the observations in the present study, there may be a therapeutic advantage to use GAD67 as a pharmacologic target for smoking-related disorders in the lung. However, while mucus overproduction is commonly associated with smoking and many COPD patients have mucus production, there is variability in the extent of mucus production among smokers and smoking-related disorders , any therapy focused on mucus overproduction would have to be tailored to the individual.
There is a complete GABAergic system in human large and small airway epithelium. Marked up-regulation of GAD67 by cigarette smoking is associated with MUC5AC overexpression. In the context of these observations, the GABAergic system is a promising pharmacological target for inhibiting airway mucus overproduction.
We thank N Mohamed for help in preparing this manuscript. These studies were supported, in part, by R01 HL074326; P50 HL084936; and UL1-RR024996.
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