Expression and function of human hemokinin-1 in human and guinea pig airways
© Grassin-Delyle et al. 2010
Received: 16 April 2010
Accepted: 7 October 2010
Published: 7 October 2010
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© Grassin-Delyle et al. 2010
Received: 16 April 2010
Accepted: 7 October 2010
Published: 7 October 2010
Human hemokinin-1 (hHK-1) and endokinins are peptides of the tachykinin family encoded by the TAC4 gene. TAC4 and hHK-1 expression as well as effects of hHK-1 in the lung and airways remain however unknown and were explored in this study.
RT-PCR analysis was performed on human bronchi to assess expression of tachykinin and tachykinin receptors genes. Enzyme immunoassay was used to quantify hHK-1, and effects of hHK-1 and endokinins on contraction of human and guinea pig airways were then evaluated, as well as the role of hHK-1 on cytokines production by human lung parenchyma or bronchi explants and by lung macrophages.
In human bronchi, expression of the genes that encode for hHK-1, tachykinin NK1-and NK2-receptors was demonstrated. hHK-1 protein was found in supernatants from explants of human bronchi, lung parenchyma and lung macrophages. Exogenous hHK-1 caused a contractile response in human bronchi mainly through the activation of NK2-receptors, which blockade unmasked a NK1-receptor involvement, subject to a rapid desensitization. In the guinea pig trachea, hHK-1 caused a concentration-dependant contraction mainly mediated through the activation of NK1-receptors. Endokinin A/B exerted similar effects to hHK-1 on both human bronchi and guinea pig trachea, whereas endokinins C and D were inactive. hHK-1 had no impact on the production of cytokines by explants of human bronchi or lung parenchyma, or by human lung macrophages.
We demonstrate endogenous expression of TAC4 in human bronchi, the encoded peptide hHK-1 being expressed and involved in contraction of human and guinea pig airways.
The mammalian tachykinins are a family of structurally related peptides which are derived from three distinct genes. TAC1 encodes for substance P (SP) and neurokinin A (NKA) through alternative splicing, while TAC3 encodes for neurokinin B (NKB) [1, 2]. TAC4 was identified recently in lymphoid B haematopoietic cells of the mouse bone marrow and encodes for hemokinin-1 (HK-1) . The same peptide is encoded by the rat TAC4  and is consequently named rat/mouse hemokinin-1 (r/mHK-1). In human, TAC4 encodes for hemokinin-1 (hHK-1), but its sequence is different from its murine counterpart. A more detailed analysis of the TAC4 gene in humans showed that it is spliced into four alternative transcripts (α, ß, γ and δ) that give rise to four different peptides which have been named endokinins, endokinin A (EKA), B (EKB), C (EKC) and D (EKD). Extensive TAC4 expression has been shown in a number of murine tissues including brain, spleen, stomach, skin, breast, bone marrow, thymus, prostate, uterus, skeletal muscle, lymph node, eyes, as well as in lung . In human, TAC4 expression has been observed in several tissues including brain, cerebellum, thymus, prostate, testis, uterus, adrenal gland, fetal liver and spleen for αTAC4; heart, liver adrenal gland, bone marrow, prostate and testis for βTAC4, whereas γ-and δTAC4 where ubiquitously expressed, with the most prolific expression in the adrenal gland and placenta [4–6]. TAC4 expression in human lung was reported in multi-tissue cDNA expression panels, but without distinction of the different anatomical entities (bronchi, parenchyma...) [4, 6].
The biological action of tachykinins are mediated by at least three different transmembrane G-protein coupled receptors, namely NK1, NK2 and NK3 receptors which are stimulated preferentially, but not exclusively by SP, NKA and NKB, respectively [7–9]. r/mHK-1 has similar affinity to SP at the human NK1 receptor [4, 6, 10–12], while hHK-1 binds to the human NK1 receptor with a 14-fold lower affinity than SP . Human HK-1 also binds to the human NK2 and NK3 receptors, with an affinity about 200-250-fold lower than for NK1 receptors [4, 10, 13].
HK-1 is involved in a variety of biological effects. Many studies have focused on its actions on immunological regulation and inflammation. Indeed, r/mHK-1 was initially found to be an important growth and survival factor for mouse early B-cells [3, 14–16] and can play a role in murine T-cell development . With respect to smooth muscle preparations, r/mHK-1 was found to cause a relaxation of the porcine coronary arteries  but to induce a contraction of the isolated rat urinary bladder , mouse and human uterus [18, 19]. hHK-1 was also able to induce coronary vasodilatation followed with coronary vasorelaxation in the isolated guinea pig heart . Numerous reports have focused on the involvement of the nonadrenergic noncholinergic system in the regulation of airway tone, demonstrating contractile properties for SP and NKA in human bronchi [21–25] and guinea pig airways [23, 26]. Tachykinins released from the sensory unmyelinated C-fibers can cause the contraction of airway smooth muscle, an increase in vascular permeability, glandular secretion, and in cholinergic neurotransmission . Tachykinins have been also involved in the recruitment and the activation of inflammatory cells such as mast cells , eosinophils , neutrophils [30, 31], lymphocytes , monocytes and macrophages . Tachykinins are also produced by immune and inflammatory cells airway smooth muscle cells, endothelial and epithelial cells, and fibroblasts [3, 14, 34–36]. This non neuronal production may be involved in the pulmonary effects of tachykinins. These peptides can induce bronchoconstriction in man, asthmatics being more sensitive than normal subjects, in agreement with the in vitro enhanced sensitivity and maximal response to tachykinins of human bronchi pretreated with serum from patients with atopic asthma . However, in contrast to the characterization of SP-or NKA-mediated effects, little is known about the expression of hHK-1 and the contractile and inflammatory effects of this peptide in human airways. Thus, the aims of the present study were to determine the presence of tachykinins, tachykinin receptors and tachykinins degrading enzyme neutral endopeptidase (NEP) mRNAs, and hHK-1 protein in human bronchial tissues, and to characterize the effects of hHK-1, EKA/B (common C-terminal decapeptide of EKA and EKB [6, 38]), EKC and EKD in human and guinea-pig isolated airways. Finally, effects of hHK-1 on the production of cytokines by explants of human bronchi or lung parenchyma and by human lung macrophages were assessed in comparison to those of SP. We report for the first time the endogenous expression of TAC4 and hHK-1 in human bronchi, together with a role of hHK-1 and endokinins in the contraction of human and guinea pig airways.
Human bronchial tissues were removed from 47 patients undergoing surgical resection at Foch Hospital (Suresnes, France) or Val d'or Clinic (Saint Cloud, France) for lung cancer (31 men and 16 women; age = 64 ± 9 years). Just after resection, segments of human bronchi with an inner diameter (ID) of 1 to 3 mm were taken as far as possible from the malignant lesion. Male Hartley guinea pigs (Charles River, L'Arbresle, France) weighing 300 to 350 g were sacrificed by cervical dislocation, and tracheas and proximal bronchi were removed. After the removal of adhering lung parenchyma and connective tissues, rings from human bronchi (5-7 mm long, 0.5-1 mm ID) and guinea pig trachea (3 mm long, 3 mm ID) or proximal airways (3 mm long, 1 mm ID) were prepared. 8 to 24 segments of human bronchi were obtained from each patient, whereas 8 trachea segments and 2 to 3 main bronchi segments were obtained from each guinea pig. For RT-PCR analysis, human bronchi were isolated within 1 hour after resection, immediately disrupted and homogenized in TRIzol reagent (Invitrogen) with a Potter Elvehjem homogenizer, and homogenates were kept frozen at -80°C until mRNA extraction. Experiments with human lung tissues were approved by the Regional Ethics Committee for Biomedical Research and animals were used as recommended by animal care guidelines.
Total RNA was extracted from human bronchi (n = 4) using TRIzol reagent. After a DNase step (DNase I, Invitrogen), total RNA (1 μg) was reverse-transcribed using a High Capacity RNA-to-cDNA Synthesis Kit (Applied Biosystems, Les Ulis, France). The resulting product (cDNA) was used as template in endpoint or real-time PCR. Amplification was performed from 20 ng cDNA with Power SYBR Green PCR Master Mix (Applied Biosystems) in a MiniOpticon Real-Time PCR Detection System (Bio-Rad, Marnes-la-Coquette, France). Thermal cycling conditions were designed as follows: initial denaturation at 95°C for 10 min, followed by 40 cycles at 95°C for 15 sec and 60°C for 1 min. Total reaction volume was 25 μL with 300 nM of each reverse and forward primer. The primers used for tachykinins and their receptors were designed against sequences common to all described isoforms and were synthesized by Eurogentec (Angers, France). The primer pairs used for PCR were as follows: 5'-AAAGGGCTCCGGCAGTTC-3' and 5'-TGCAGAAGAAATAGGAGCCAATG-3' for TAC1; 5'-GAAGTCATGCATGTCACGTTTCTC-3' and 5'-GACTCTTCAAAAGCCACTCATCTCT-3' for TAC3; 5'-TACGGCGAAGCTGTGCATT-3' and 5'-TCACACAAGGCCCACACTGA-3' for TAC4; 5'-GTAGGGCAGGAGGAAGAAGATGT-3' and 5'-CAAGGTGGTCAAAATGATGATTGT-3' for TACR1; 5'-GAGGCCGATGACGCTGTAG-3' and 5'-CAAGACGCTCCTCCTGTACCA-3' for TACR2; 5'-ATATACCTGTCCACCGCAATGG-3' and 5'-CGCTTCCAGAACTTCTTTCCTATC-3' for TACR3. Expected amplicon sizes were 91, 110, 90, 85, 84 and 80 bp respectively. For NEP, primer pair was 5'-GGAGCTGGTCTCGGGAATG-3' and 5'-AGCCTCTCGGTCCTTGTCCT-3'  (amplicon expected size: 219 bp). To control for the recovery of intact cellular RNA and for the uniform efficiency of each reverse transcription reaction, a hypoxanthine phosphoribosyltransferase (HPRT) fragment was amplified by real-time RT-PCR (primer pair: 5'-TAATCCAGCAGGTCAGCAAAG-3' and 5'-CTGAGGATTTGGAAAGGGTGT-3'; expected size: 157 bp) on the same plate as that with tachykinins or tachykinins receptors cDNAs. The absence of secondary, non-specific amplification products in our experiments was assessed by analyzing melting curves and by separating PCR reaction products on agarose gel. The identity of each PCR product was established by DNA sequence analysis. With each sample, control samples without the RT step or with water instead of cDNA template were amplified to ensure there was no genomic DNA contamination and that all reagents were free of target sequence contamination. For each tachykinin and tachykinin receptor gene, a positive control sample of human fetal brain total mRNA (Ozyme, Saint Quentin en Yvelines, France) was also included in each run.
Human bronchial rings and guinea pig tracheal and bronchial rings were suspended on hooks in 5 mL organ bath containing a modified Krebs-Henseleit solution (NaCl 119, KCl 4.7, CaCl2 2.5, KH2PO4 1.2, NaHCO3 25 and glucose 11.7 mM), maintained at 37°C and oxygenated with 95% O2 and 5% CO2. An initial tension of 2 g was applied to tissues, according to previously described protocols [21, 26]. Changes of tension were measured isometrically with Gould strain gauges (UF1; Piodem, Canterburry, Kent, UK); and were recorded and post-processed with IOX and Datanalyst softwares (Emka Technologies France, Paris). During the initial stabilization period (30 min), tissues were washed every 10 minutes with Krebs-Henseleit solution. Phosphoramidon was used to inhibit enzymatic degradation of tachykinins by NEP [21, 40]. Phosphoramidon (10-6 M) was added in organ bath with or without NK1-, NK2- or NK3-receptor antagonists (SR 140333, SR 48968 and SR 142801, 10-7 M) after the first stabilization period. Antagonist concentrations were chosen based on their reported affinities for human tachykinin receptors [41–43] and on their ability to antagonize HK-1-induced responses at similar concentrations in other models [10, 13, 44]. Tissues were then equilibrated 1 hour and concentration-response curves to tachykinins and related peptides were established by applying cumulative concentrations of peptides at 5 to 10 min intervals in semi-logarithmic increments, or by applying a single concentration of peptide. Only one concentration-response curve to tachykinins was recorded in each strip, and each experiment was performed in duplicate. Maximal response was determined by a final addition of acetylcholine hydrochloride (ACh, 3 mM). Contractile responses to tachykinins and related compounds were expressed as percentage of that induced by ACh. The pD2 (defined as the negative log of the molar drug concentration that caused 50% of maximal effect) were calculated from the log concentration-effect curves. When the pD2 value was not assessable (maximal effect (Emax) not reached), it was replaced by the -log EC20 (defined as the negative log of the drug concentration that caused 20% of maximal contraction with ACh). All values in the text and in the figures are expressed as arithmetic mean ± standard error of the mean (s.e.m) of duplicate experiments on tissues from the given (n) number of individuals or animals.
Explants of lung parenchyma and bronchi were prepared according to Mitsuta et al. . Briefly, small bronchi (1 mm ID) removed from 4 patients and lung parenchyma from 6 patients were cut under sterile conditions into small fragments and rinsed once in RPMI 1640 supplemented with antibiotics (100 μg/mL streptomycin and 100 U/mL penicillin) and 2 mM L-glutamine. Explants were then conserved overnight at +4°C in RPMI supplemented medium. Fragments (≈ 50 mg) were pre-incubated in 12-well (bronchi) or 6-well (parenchyma) culture plates for 1 hour (37°C, 5% CO2) in the presence of phosphoramidon (10-6 M) in 2.5 mL (bronchi) or 5 mL (parenchyma) of RPMI supplemented medium, before hHK-1 or SP (both 10-9 to 10-5 M) was applied.
Lung macrophages from 6 patients were isolated and cultured as previously described  and exposed to either hHK-1 or SP (both 10-9 to 10-5 M) after a 1-hour pre-incubation with phosphoramidon (10-6 M). After a 24 hour incubation of bronchi and parenchyma explants or lung macrophages, supernatants were collected, centrifuged and frozen at -80°C until subsequent cytokine quantification.
Cytokines production (TNF-α, IL-6, IL-8, MIP-1α, MCP-1, ENA-78, GRO-α, MIG, and MIF) was assessed by measuring their concentrations in the culture supernatants with enzyme-linked immunosorbent assays (ELISA, Duoset Development System), according to the manufacturer's instructions (R&D Systems Europe, Lille, France). hHK-1 concentrations were determined with enzyme immunoassay (EIA) according to the manufacturer's instructions (Bachem, Weil am Rhein, Germany). Specifications of this EIA indicate absence of cross-reactivity with SP, NKA or NKB, and appropriate negative (RPMI alone) and positive (RPMI spiked with hHK-1) controls were included in the assay. Supernatants were diluted as appropriate and the optical density was determined at 450 nm with an MRX II microplate reader from Dynex Technologies (Saint-Cloud, France). Concentrations were expressed as pg per 100 mg tissue (bronchi and parenchyma explants) or pg per million cells (lung macrophages). The detection limits of these assays were 8 pg/ml for MIP-1α, 9 pg/ml for IL-6, 16 pg/ml for TNF-α, MCP-1 and ENA-78, 32 pg/ml for IL-8, GRO-α and MIF, and 62 pg/ml for MIG.
Substance P (RPKPQQFFGLM-NH2), [Sar9,Met(O2)11] substance P (selective for NK1 receptors), neurokinin A (HKTDSFVGLM-NH2), [β-Ala8]-NKA (4-10) (selective for NK2 receptors), neurokinin B (DMHDFFVGLM-NH2) were provided from Bachem and human hemokinin-1 (TGKASQFFGLM-NH2) from NeoMPS (Strasbourg, France). Custom synthesized endokinin A/B, endokinin C and endokinin D were supplied from Phoenix Pharma (Belmont, California, USA), SR 140333 ((S)1-(2-[3-(3,4-dichlorophenyl)-1-(3-isopropoxyphenylacetyl)piperidin-3-yl] ethyl)-4-phenyl-1-azoniabicyclo [2.2.2]octane chloride), SR 48968 ((S)-N-methyl-N-[4-acetylamino-4-phenylpiperidino-2-(3,4-dichlorophenyl) butyl]benzamide) and SR 142801 ((S)-(N)-(1-(3-(1-benzoyl-3-(3,4-dichlorophenyl)piperidin-3-yl)propyl)-4-phenylpiperidin-4-yl)-N-methylacetamide) were kindly provided by Dr Emonds-Alt (Sanofi Research Center, Montpellier, France) and dissolved in ethanol. Phosphoramidon (N-(α-L-rhamnopyranosyloxyhydroxyphosphinyl)-L-leucyl-L-tryptophan), penicillin/streptomycin stabilized solution, L-glutamine and acetylcholine hydrochloride were obtained from Sigma (Saint Louis, MO, United States); RPMI 1640 medium from Eurobio Biotechnology (Les Ulis, France). All tachykinins except NKB were dissolved in sterile distilled water and kept in aliquots at -20°C until used. Solutions of NKB were prepared in 20% dimethylsulfoxide and then diluted in distilled water. Maximal final concentrations of dimethylsulfoxide achieved in organ baths were found to have no effect on resting bronchial tone and on acetylcholine-induced responses.
GraphPad Prism software (version 5.01 for Windows, GraphPad Software®, San Diego California, United States) was used to determine pD2 and Emax and to perform a statistical analysis of the results, using ANOVA followed with Bonferroni post-tests. A p value lower than 0.05 (p < 0.05) was considered to be significant.
In addition to TAC4 mRNA expression, hHK-1 protein was found in the supernatants of bronchial explants (1.40 ± 0.31 pg/100 mg (n = 11)), parenchyma explants (1.15 ± 0.29 pg/100 mg (n = 11)) and lung macrophages (1.85 ± 0.89 pg/106 cells (n = 6)) cultured for 24 hours in the presence of phosphoramidon.
The NK2 receptor antagonist SR 48968 (10-7 M), completely abolished the contractile effects of cumulative additions of hHK-1 on human isolated bronchi, whereas the NK1 receptor antagonist SR 140333 (10-7 M) only exerted a small but not statistically significant reduction of hHK-1-induced contraction at the lowest concentrations (10-8 M-10-7 M) (fig. 2A). Finally, the NK3 receptor antagonist SR 142801 (10-7 M) did not alter the concentration-response curve to hHK-1.
Functional potencies and maximal effects of human hemokinin-1 and various tachykinin peptides on guinea-pig trachea.
Emax (% of Ach 3 mM)
6.4 ± 0.03
73 ± 5
6.7 ± 0.1
84 ± 2
7.5 ± 0.1
76 ± 2
8.1 ± 0.1
95 ± 2
8.3 ± 0.6
80 ± 5
hHK-1 and SP up to 10-5 M had no impact on TNF-α, IL-8 and MIP-1α production by bronchial explants (n = 4). Similarly, both peptides did not alter TNF-α, IL-6, MIP-1α, MCP-1, ENA-78, GRO-α, MIG, and MIF production by lung parenchyma (n = 6 different preparations) and TNF-α, IL-6, MIF, MIG and MIP-1α production by lung macrophages (n = 3 to 6 different preparations) (data not shown). LPS caused a clear-cut increase of these cytokines in all preparations.
In the present study we have demonstrated the expression of TAC4 transcript and protein in human bronchi and shown that hHK-1 and EKA/B exert a contractile effect in human and guinea pig airways. In human isolated bronchi, the response is mediated mainly through NK2 receptor stimulation, the NK1 receptor-mediated effect being unmasked in the presence of SR 48968 and subject to rapid desensitization. In guinea pig trachea and main bronchi, the response is mediated mainly through NK1 receptor stimulation and to a minor extent through NK2 receptors. The N-terminally extended form of human hHK-1, EKA/B, exerts similar effects to hHK-1 on both human bronchi and guinea pig airways, whereas EKC and EKD, peptides also derived from TAC4, did not induce functional responses. Finally, we have shown that hHK-1 did not alter cytokine production by human bronchi or parenchyma explants, or by human lung macrophages.
Our study shows that the TAC4 gene encoding for hHK-1 is constitutively present and expressed in human airways. Only a few numbers of studies have been devoted to the presence of TAC4 in human tissues, particularly in lung, and none of them has previously reported expression of hHK-1 protein. Indeed, TAC4 expression was not found in the mouse lung by northern blot analysis , but was demonstrated by semi-quantitative PCR in murine lung (mouse, gerbil) [4, 5]. In human, a wide expression of TAC4 has been reported with a strong expression in tissues such as heart, skeletal muscle, skin, thyroid, spinal cord, placenta, adrenal gland, spermatozoa and blood circulating cells and a weaker expression in whole lung, kidney, testis and liver [4, 6, 39, 47]. In contrast to TAC4, we have shown that TAC1, which encodes for SP and NKA, was not detected under our experimental conditions and that TAC3 was observed in only one of four samples. In a previous study, Pinto et al. showed in a human total mRNA master panel (BD Biosciences Clontech) that TAC1 and TAC3 mRNAs were undetectable in the lung, but they observed a low expression of these transcripts in samples of human bronchi obtained from patients who had undergone lobectomy or pneumectomy for lung carcinoma, a high expression being observed in pulmonary arteries . Concerning the genes that encode for tachykinin receptors, we have identified the mRNA expression of TACR1 (NK1 receptor) and TACR2 (NK2 receptor), in agreement with Pinto et al. and in agreement with previous immunohistochemical evidences of NK1 and NK2 receptor expressions in human bronchial smooth muscle, bronchial glands and bronchial vessels [48, 49]. We did not find TACR3 (NK3 receptor) expression whereas Pinto et al. identified this transcript in all assayed tissues . These discrepancies in the results of tachykinin transcript expression could be related to differences either within human samples or to differences in expression patterns of tachykinin genes along the respiratory tract since we used smaller bronchi than in the work of Pinto et al. and since differences in the response to tachykinins have been reported according to the size of human bronchi . It should be noted that we found TAC4 transcript and hHK-1 protein expressions in human bronchi similar in size (1 to 3 mm) to the bronchi used for the functional studies, substantiating a role for hHK-1 in the regulation of airway tone. Finally, our results showing NEP mRNA expression are also consistent with previous studies reporting a strong expression of NEP in human bronchi .
In human isolated bronchi pre-treated with phosphoramidon, hHK-1 exerts a contractile effect which was abolished by the NK2 receptor antagonist SR 48968, while the NK1 receptor antagonist SR 140333 only weakly reduced the effects of hHK-1 at low concentrations. In human bronchi, hHK-1 appears 800-fold less potent than NKA. This result is in agreement with previous data obtained on NK2 receptors either with CHO cells  or rabbit pulmonary artery .
A rapid functional desensitization of NK1 receptors has been reported with SP and specific NK1 receptor agonists in different tissues [51, 52] including airways . In addition, HK-1 has been reported to induce a desensitization of NK1 receptors in human embryonic kidney cells , rabbit jugular veins , U251 MG astrocytoma cells  and scratching behavior in rats . We also observed desensitization of NK1 receptors in human bronchi, since the magnitude of the contractile response caused by the second application of the NK1-receptor specific agonist was lower than after the first addition, even with a 10-fold higher concentration. Such a desensitization can be due to receptor internalization, which is a common phenomenon for NK1 receptor signaling  and has already been described with hHK-1 on astrocytoma cells . We have demonstrated a cross-desensitization between hHK-1 and [Sar9, Met (O2)11] SP substantiating NK1-receptor activation and desensitization by hHK-1. In addition, since a first exposure to [Sar9, Met (O2)11] SP was able to desensitize the NK1 receptor, preventing a second response to this specific NK1-receptor agonist, but was unable to prevent the response to hHK-1, these cross-desensitization experiments further substantiate the NK2-receptor mediated component of the contractile response to hHK-1. As expected in the single addition protocol, the contractile effect of [Sar9,Met(O2)11] SP was abolished by the NK1 receptor antagonist SR 140333 and unmodified by the NK2 receptor antagonist SR 48968. In contrast, the effect of hHK-1 was not inhibited by SR 140333 or SR 48968 when used alone, but was abolished by concomitant addition of the two antagonists, demonstrating that hHK-1 contracts bronchi through NK1- and NK2 receptors. However, it can also be suggested that [Sar9,Met(O2)11] SP and SP on the one hand, and hHK-1 on the other hand, may bind to different sites of the NK1 receptor and interact in a different manner with receptor antagonists [5, 56].
In contrast with the results in human bronchi, SP and the specific NK1-receptor agonist produced maximal responses similar to those of NKA and hHK-1 in guinea pig airways providing evidence of the higher involvement of NK1 receptors in this animal species than in humans as already reported [23, 40]. In support of this notion, hHK-1 exerted a contractile effect mainly through NK1 receptor stimulation since this effect was abolished by the NK1 receptor antagonist SR 140333, but was only weakly reduced in the presence of the NK2 receptor antagonist SR 48968. However, the NK2 receptors play a predominant role in guinea pig airways contraction since NKA is approximately 10-fold more potent than SP [23, 40]. The weak effect of SR 48968 against hHK-1 induced bronchoconstriction in the guinea pig airways is likely explained by the higher affinity of hHK-1 for NK1- than for NK2 receptors in a preparation fully responsive to NK1-mediated response [4, 10, 13]. It is noteworthy that the potency of hHK-1 in the guinea pig airways was lower than that reported for r/mHK-1 in specific NK1-receptor animal tissues such as rabbit jugular vein , rat urinary bladder  and pig coronary artery .
In our study of cytokines production, we were not able to reproduce the weak TNF-α production that was observed in SP-stimulated human alveolar macrophages from healthy subjects . This result may be related to the underlying disease or the smoking status of the patients that were all ex-smokers in our study since SP-induced TNF-α release is more pronounced in smokers . SP-induced release of inflammatory mediators by human monocytes/macrophages still remains controversial and may have been related to the presence of endotoxin at low levels [58–61]. In addition to the lung macrophages, explants of lung parenchyma and bronchi did not produce pro-inflammatory cytokines in response to hHK-1 or SP, suggesting that hHK-1 may not be involved in lung inflammatory pathways through the release of these cytokines. However, hHK-1 may exert other inflammatory effects as already described for SP or NKA (reviewed in ).
SP expression has been reported in the human respiratory tract  and is increased in airways , bronchoalveolar or nasal lavages , sputum  or plasma  from asthmatics. It has been demonstrated that the antibodies used in such studies were directed against the C-terminal portion of SP, which is shared by hHK-1, leading to cross-reactivity with hHK-1 . Immunoreactivity attributed to SP expression in human lungs may therefore be also related to hHK-1 expression. The use of specific assays for hHK-1 is required to evaluate the respective expression of SP and hHK-1 in the respiratory tracts of healthy subjects and in patients with asthma.
In conclusion, our results provide evidence for a constitutive expression of TAC4 and hHK-1 in human bronchi. Our findings indicate that hHK-1 could induce contraction of human bronchi and guinea pig airways. This hHK-1-induced contraction could be mainly attributed to NK2 receptors in humans and to NK1 receptors in guinea pig. The absence cytokine release from lung explants and macrophages suggests that hHK-1 does not participate in airways inflammation by inducing the release of the pattern of cytokines measured in the present study. hHK-1 is therefore involved in the tachykinin-driven contractile response of human airways, but further studies are needed for a better understanding of hHK-1 involvement in airway diseases such as asthma.
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