Synergistic effect of interleukin 1 alpha on nontypeable Haemophilus influenzae-induced up-regulation of human beta-defensin 2 in middle ear epithelial cells
© Moon et al; licensee BioMed Central Ltd. 2006
Received: 05 August 2005
Accepted: 24 January 2006
Published: 24 January 2006
We recently showed that beta-defensins have antimicrobial activity against nontypeable Haemophilus influenzae (NTHi) and that interleukin 1 alpha (IL-1 alpha) up-regulates the transcription of beta-defensin 2 (DEFB4 according to new nomenclature of the Human Genome Organization) in human middle ear epithelial cells via a Src-dependent Raf-MEK1/2-ERK signaling pathway. Based on these observations, we investigated if human middle ear epithelial cells could release IL-1 alpha upon exposure to a lysate of NTHi and if this cytokine could have a synergistic effect on beta-defensin 2 up-regulation by the bacterial components.
The studies described herein were carried out using epithelial cell lines as well as a murine model of acute otitis media (OM). Human cytokine macroarray analysis was performed to detect the released cytokines in response to NTHi exposure. Real time quantitative PCR was done to compare the induction of IL-1 alpha or beta-defensin 2 mRNAs and to identify the signaling pathways involved. Direct activation of the beta-defensin 2 promoter was monitored using a beta-defensin 2 promoter-Luciferase construct. An IL-1 alpha blocking antibody was used to demonstrate the direct involvement of this cytokine on DEFB4 induction.
Middle ear epithelial cells released IL-1 alpha when stimulated by NTHi components and this cytokine acted in an autocrine/paracrine synergistic manner with NTHi to up-regulate beta-defensin 2. This synergistic effect of IL-1 alpha on NTHi-induced beta-defensin 2 up-regulation appeared to be mediated by the p38 MAP kinase pathway.
We demonstrate that IL-1 alpha is secreted by middle ear epithelial cells upon exposure to NTHi components and that it can synergistically act with certain of these molecules to up-regulate beta-defensin 2 via the p38 MAP kinase pathway.
Following the common cold, otitis media (OM), or inflammation of the middle ear, is the most frequent illness resulting in visits to physicians and the most common cause of hearing impairment in children . The majority of the cases of OM are caused by three pathogens: Streptococcus pneumoniae, nontypeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis [2, 3].
Bacterial adherence to mucosal surfaces is a first step in respiratory infections. NTHi, S. pneumoniae and M. catarrhalis have all been shown to adhere to human upper respiratory epithelial cells [4–10]. Li and colleagues demonstrated that NTHi binds to and activates toll-like receptor 2 (TLR2) on the surface of epithelial cells . The TLRs have been shown to be involved in the activation of many host genes, including cytokines, chemokines and antimicrobial peptides such as β-defensin 2 [12–14].
The defensins are cationic (polar) molecules with spatially separated hydrophobic and charged regions. In vitro, the defensins (at micromolar concentrations) have a broad spectrum of antimicrobial activity against bacteria, fungi, and even some enveloped viruses [15, 16]. In humans and other vertebrates, the defensins can be divided into the α- and β-defensin subfamilies on the basis of the position and bonding of six conserved cysteine residues. The α-defensins are produced by neutrophils and intestinal Paneth's cells . The β-defensins, on the other hand, are mainly produced by epithelial cells of the skin, kidneys, and trachea-bronchial lining of nearly all vertebrates [18–20]. Multiple β-defensin genes have been identified and three have been characterized at the peptide level [21–23]. β-defensin 1 is expressed constitutively by variety of cell types, while β-defensin 2 expression is highly up-regulated by exposure to inflammatory stimuli such as bacterial components or proinflammatory cytokines [24, 25].
We have recently shown that both human β-defensin 1 and 2 have bactericidal /bacteriostatic activity against NTHi . Moreover, in another study, we demonstrated that IL-1α can upregulate the transcription of β-defensin 2 in human middle ear epithelial cells, mediated by a Src-dependent Raf-MEK1/2-ERK signaling pathway . In accord with our observations, IL-1α has also shown to be a potent activator of β-defensin 2 in intestinal epithelial cells . Furthermore, the biological relevance of IL-1α as an inducer of β-defensin 2 in the tubotympanum has been demonstrated in in vivo studies that have shown IL-1α to be one of the cytokines induced in a rat model of OM .
In the present study we demonstrate that NTHi treatment of human middle ear epithelial cells results in release of IL-1α and that this cytokine and NTHi can synergistically up-regulate human β-defensin 2 (DEFB4) expression. Here, a note should be added regarding the new nomenclature of the b-defensin family of molecules http://www.gene.ucl.ac.uk/cgi-bin/nomenclature/searchgenes.pl. Human b-defensin 2 is now called DEFB4 and its mouse orthologue is called b-defensin 4 (Defb4). This change has created some confusion in the scientific community. Thus, to avoid confusion and remain consistent with the nomenclature used in our previous studies, will continue to refer to molecule under investigation as b-defensin 2.
Recombinant interferon-γ-inducible protein-10 (IP-10), regulated upon activation, normally T-expressed, and presumably secreted (RANTES), interleukin (IL)-1α, IL-6, IL-8 and macrophage inflammatory protein-1β (MIP-1β) were purchased from Sigma (St. Louis, MO). PD98059 (ERK MAP kinase inhibitor), SB203580 (p38 MAP kinase inhibitor), and SP600125 (Jun N-terminal kinase inhibitor) were purchased from Calbiochem (San Diego, CA).
Preparation of bacterial lysate
NTHi strain 12, originally a clinical isolate from the middle ear fluid of a child with acute otitis media, was used in this study . A single colony of NTHi was harvested from a chocolate agar plate, inoculated into 30 ml of brain heart infusion broth supplemented with nicotinamide adenine dinucleotide (3.5 μg/ml) and placed in a shaking incubator overnight. The supernatant was discarded after centrifugation at 10,000 × g for 10 minutes. The pellet was resuspended in 10 ml of phosphate-buffered solution (PBS) and sonicated to lyse the bacteria. The lysate was then centrifuged at 10,000 × g for 10 min and the supernatant was collected. The protein concentration of the NTHi lysate was determined using the Bicinchoninic (BCA) protein assay and was in the range of 0.15 mg/ml.
The human middle ear epithelial cell line (HMEEC), immortalized with the E6/E7 genes of human papilloma virus type 16 , was maintained in a 1:1 mixture of Dulbecco's modified Eagle's medium (DMEM) (Invitrogen, Carlsbad, CA) and bronchial epithelial basal medium (Clonetics, Walkersville, MD) supplemented with bovine pituitary extract (52 μg/ml), hydrocortisone (0.5 μg/ml), hEGF (0.5 ng/ml), epinephrine 0.5 (mg/ml), transferrin (10 μg/ml), insulin (5 μg/ml), triiodothyronine (6.5 ng/ml), retinoic acid (0.1 ng/ml), gentamycin (50 μg/ml), and amphotericin-B (50 ng/ml). Hela (human cervix epithelial) cells and A549 (human lung epithelial) cells were purchased from the ATCC (Manassas, VA), and maintained in DMEM containing 10% fetal bovine serum (Invitrogen), penicillin (100 units/ml), and streptomycin (0.1 mg/ml). For studying the effect of NTHi and IL-1α, the cells were seeded into six-well plates in triplicate, and were pretreated for one hour with or without chemical inhibitors of MAP kinase including PD98059, SB203580, and SP600125. All cells were maintained in a humidified atmosphere of 5% CO2 and 95% air.
Eighteen, 10 week-old male C57BL/6 mice were used in this study. Three mice were for each time point including two control groups: non-treated and PBS-inoculated.
All aspects of animal handling were performed according to approved IACUC guidelines. The mice were transtympanically inoculated with 10 μl of the NTHi lysate (1:10 dilution) after anesthesia with Ketamine (5 mg/100 g). Middle ear mucosal RNA was then harvested at 6, 9, 12 and 24 hours post inoculation by irrigation of the bulla with three, 3.5 μl Trizol washes (Invitrogen). Briefly, the mice were anesthetized using Ketamine (5 mg/100 g), and then decapitated. A small incision (1 cm) was made in the retroauricular area and the cortical bone of the bulla was exposed after dissection. A hole, sized 2 mm × 2 mm, was made using the sharp scalpel followed by irrigation of the bulla with Trizol. The total Trizol volume was then increased to 200 μl and RNA was precipitated per the manufacturer's instructions. The middle ear mucosa was inflamed in all NTHi-treated mice, but effusion was not seen in all groups. No sepsis or death occurred as a result of the experimental treatment.
A solid phase multiplexed protein assay in a sandwich ELISA format was performed to detect various cytokines simultaneously. Briefly, HMEEC medium was harvested 48 hours after treatment with NTHi or PBS. Pre-blotted membranes with various anti-cytokine antibodies in the BioSource Human Cytokine Set 1 Cartesian Array™ (BioSource, Camarillo, CA) were incubated with culture medium for 2 hours at room temperature after blocking nonspecific binding sites per the manufacturer's instructions. After adding a biotin-conjugated anti-cytokine antibody mixture (provided in the kit), the membrane was incubated with HRP-conjugated streptavidin per the manufacturer's instructions. Signal intensity was quantified by densitometry.
Quantitation of IL-1α
Released IL-1α was measured using Human IL-1α ELISA Kit (Endogen) according to the manufacturer's instructions. Briefly, HMEEC medium was added into anti-human IL-1α precoated 96-well plates and incubated for one hour at room temperature. After adding biotinylated anti-cytokine antibody (provided in the kit), the 96-well plate was incubated with streptavidin-HRP solution for 30 minutes. Color was developed with TMB substrate solution after washing and the absorbance was measured at 450 nm minus 550 nm. The amount of IL-1α in unknown samples was determined after calculating the standard curve of reconstituted IL-1α diluents.
Reverse transcription and real time quantitative PCR
Total RNA was extracted using the RNeasy kit (Qiagen, Valencia, Ca) and cDNA was synthesized using the TaqMan reverse transcription kit (Applied Biosystems, Foster City, CA). Taqman primers and probes for β-defensin 2 (DEFB4) (ABI assay number Hs00823638_m1 (NM_004942)), IL-1α (ABI assay number Hs00899844_m1 (NM_000575)) and cyclophilin D (ABI assay number Hs00234593_m1 (NM_005038)) were purchased from Applied Biosystems. Multiplex PCR was performed using 7500 Real Time PCR System (Applied Biosystems) and cycle threshold (CT) values were analyzed. CT values of DEFB4 or IL-1α were normalized with the internal control, and results were expressed as a fold-induction of mRNA quantity, taking the value of the non-treated group as 1.
Promoter construct of DEFB4
Reporter construct of β-defensin 2 promoter (p2.7hBD2-luc) was generated as described . Briefly, 5' flanking region (from -2625 to + 1) of β-defensin 2 (DEFB4) (AF_071216) was isolated by PCR amplification with the following primers: 5'-GAG GTA CCT CCA TCC TTT ACT GTG ATG ATG CC-3' (forward primer with Kpn1 tail), 5'-GAA AGC TTT GGC TGA TGG CTG GGA GCT TCA CCA (reverse primer with HindIII tail). The amplified product was subcloned into the multiple cloning site of the pGL3-Basic luciferase reporter plasmid (Promega, Madison, WI). The reporter construct was sequenced to verify number and orientation of inserted oligonucleotides.
Transfection and Luciferase assay
All transient transfections were carried out in triplicate using TransIT-LT1 (Panvera, Madison, WI) according to the manufacturer's instructions. Cells were seeded into six-well plates at a density of 1.5 × 105 cell/well, and were transfected with p2.7hBD2-luc plasmid upon reaching 60% confluence. The transfected cells were not selected with antibiotics. NTHi lysate or IL-1α was added to the transfected cells 40 hrs post transfection. Cells were harvested after 8 hrs, and luciferase activity was measured using a luminometer (Pharmingen, La Jolla, CA) after mixing with luciferase substrate (Promega), per the manufacturer's instructions. The results were expressed as fold increase of luciferase activity, compared to non-treated controls.
Blocking the effects of epithelial cell-derived IL-1α
Cell culture medium was collected 48 hrs after treatment with NTHi lysate. The medium was briefly centrifuged to remove the cellular debris and diluted 1:4. The diluted medium was then incubated with an anti-interleukin 1α antibody (20, 40 and 80 μg/ml) (Endogen, Woburn, MA) or with non-immunized rabbit IgG (20 μg/ml) (Sigma) for 30 min at room temperature. The antibody treated medium was then used to replace the medium on HMEEC transfected with the DEFB4 promoter construct. Cells were harvested after 8 hrs, and luciferase activity was measured as described above.
All experiments were carried out in triplicate. Results are expressed as mean ± standard deviation. Statistical analysis was performed using Student's t-test, with significance considered to be p < 0.01 or p < 0.05.
Release of cytokines by NTHi lysate treatment in the middle ear epithelial cells and their effect on β-defensin 2 expression
Upregulation of IL-1α by NTHi treatment in the middle ear epithelial cells
Synergistic effect of IL-1α on NTHi-induced β-defensin 2 upregulation
Inhibition of the effect of epithelial cell-derived β-defensin 2 inducing factor
Our results suggest that middle ear epithelial cells release IL-1α when stimulated by NTHi components and that this cytokine acts in an autocrine/paracrine synergistic manner with NTHi to up-regulate β-defensin 2. Furthermore, in contrast to IL-1α that acts via the ERK MAP kinase pathway to induce β-defensin 2 transcription, the synergistic effect of this cytokine on β-defensin 2 up-regulation by NTHi molecules appears to be mediated by the p38 MAP kinase pathway (Figure 6). Such synergism may be a way of boosting the epithelial cells' initial response to NTHi and its components.
The signaling mechanisms appear to be more complicated in the presence of both exogenous and endogenous inducers. NTHi, an exogenous inducer and TNF-α, an endogenous inducer synergize with each other to induce NF-κB activation and consequently up-regulate inflammatory mediators including IL-1β and IL-8 as well as TNF-α . NTHi first interacts with its receptors of host cells such as Toll-like receptor 2 (TLR2) , and leads to the activation of multiple signaling cascades resulting in the up-regulation of inflammatory cytokines such as TNF-α. The up-regulated TNF-α in response to NTHi synergize with NTHi to induce NF-κB via two distinct signaling pathways, the NIK-IKK-IκBα and the MEKK1-MKK3/6-p38 MAPK pathways .
Strains of NTHi, a small gram-negative bacterium, exist as commensal organisms in the human nasopharynx . Nasopharyngeal colonization of NTHi may persist for prolonged periods of time, even in the antibody-containing mucosal secretions since the bacteria undergo antigenic variation. This can occur by several molecular mechanisms such as point mutation, gene amplification, phase variation or horizontal gene transfer and homologous recombination . Although NTHi rarely causes life-threatening infections, it is nonetheless a clinically important pathogen since it causes otitis media in children and exacerbates chronic obstructive pulmonary disease in adults [35, 36]. The interactions between NTHi and the host are not well understood. These interactions determine chronic colonization with or without inflammation or disease. The interaction of NTHi antigens and specific host molecules are likely to be involved in the transition of NTHi from a commensal to a pathogenic organism. Further studies are, however, needed to elucidate these mechanisms.
Our results showed that the induction of β-defenin 2 by NTHi is not a pan-epithelial response, in that Hela and A549 cells do not highly respond to NTHi lysates, whereas HMEEC cells do. In addition, although NTHi treatment up-regulated IL-1α expression in Hela, A549 and HMEEC cells, treatment of the cells with IL-1α resulted in the up-regulation of β-defensin 2 only in A549 and HMEEC, but not in Hela cells. These results indicate that expression patterns of receptors or signaling molecules is cell-specific and thus determines the responses to extracellular stimuli. Our results are in agreement with earlier reports of the hypo-responsiveness of A549 cells to lipopolysaccharide (LPS), and of A549 and normal human bronchial epithelial cells to Gram-positive group B Streptococci [37, 38]. A deficiency in the expression of TLR2 and 4 may also explain the lack response of these cells to NTHi as well. Our experimental observation of the non-responsiveness of Hela cells to NTHi, is on the other hand different from previous observations demonstrating transcriptional up-regulation of β-defensin-2 by LPS  or activation of NF-κB by NTHi . This apparent difference, however may be explained by Mineshiba and colleagues' use of LPS and the fact that Shuto and coworkers studied the nuclear translocation of NF-κB, which may not be in itself sufficient for the transcriptional activation of β-defensin-2 in Hela cells.
Although the autolysis of NTHi has not been documented, it is likely that NTHi undergoes autolysis similar to that seen with Haemophilus influenzae type b , S. pneumoniae  or E. coli . Cytoplasmic, as well as membrane components of NTHi are thought to persist in the effusion and act as long lasting inducers of inflammation. This notion is supported by the fact that bacterial DNA is detectable in most sterile effusions , whereas endotoxin is detectable in 60% of the cases . While the molecules (possibly surface antigens) of intact NTHi have been demonstrated to induce proinflammatory cytokines in human respiratory epithelial cells , other studies have shown that the cytoplasmic fraction of lysed NTHi also contains important molecules for stimulating epithelial cells [46, 47]. The NTHi lysate used in this study was prepared by sonification of the bacteria and mimics normal pathophysiology.
Interleukin 1 is a central mediator of the inflammatory response and occurs in two forms. Although the acidic form, known as IL-1α, and the neutral form, IL-1β, only share 45% homology at the nucleic acid level, both proteins bind to the same receptor [48, 49]. Furthermore, both proteins are pleiotropic and affect processes such as inflammation, immunity and hemopoiesis. Moreover, while IL-1β is active only in its secreted form, IL-1α is active as an intracellular precursor, a membrane-associated cytokine, as well as a secreted molecule.
Our results suggest a role for IL-1α but not IL-1β in the up-regulation of β-defensin 2 transcription. These results are consistent with the observations that IL-1α and not IL-1β, released from epithelial cells infected with respiratory syncytial virus, enhanced expression of intercellular adhesion molecule-1 in pulmonary epithelial cells . Moreover, our data suggest that the induction of IL-1α production in middle ear epithelial cells and the autocrine/paracrine effect of this molecule may be one of the central events involved in the up-regulation of chemotactic factors for the recruitment of immune cells into the middle ear. It should be noted that although the concentration of IL-1α released into the culture medium was less than 100 pg/ml/106 cells, since the molecule is acting in an autocrine manner, its effective concentration is likely to be much higher locally.
In our previous studies, we demonstrated that IL-1α could up-regulate β-defensin 2 transcription via a Src-dependent MEK1/2-ERK1/2 signaling pathway . Interestingly however, the present study shows that the p38 MAP kinase, not the ERK1/2 pathway is involved in synergism of IL-1α and NTHi components. Moreover, our preliminary results suggest that the p38 MAP kinase pathway is involved in the activation of β-defensin 2 transcription by NTHi (unpublished data). We postulate that the activation of ERK and p38 MAP kinase pathways can result in a synergistic up-regulation of β-defensin 2. These results point to the complexity of the signaling pathways that control the expression of innate immune molecules such as β-defensin 2 and indicate the need for further investigation into the regulation of β-defensin 2 by NTHi and IL-1α.
We demonstrate that epithelial cell-derived IL-1α can synergistically act with NTHi components to up-regulate human β-defensin 2 (DEFB4) via the p38 MAP kinase pathway.
List of abbreviations
nontypeable Haemophilus influenzae
- MAP kinase:
mitogen-activated protein kinase
extracellular signal-regulated kinase
regulated upon activation, normally T-expressed, and presumably secreted
macrophage inflammatory protein
human middle ear epithelial cell line
We thank Dr X.X. Gu, NIDCD, NIH for providing the NTHi strains. This work was supported by a grant from the NIH, NIDCD (2 R01 DC005025-04) to DJL.
- Fria TJ, Cantekin EI, Eichler JA: Hearing acuity of children with otitis media with effusion. Arch Otolaryngol. 1985, 111 (1): 10-16.View ArticlePubMed
- Bluestone CD, Klein JO: Otitis Media in Infants and Children. 1995, Philadelphia , Saunders, 2nd edition
- Block SL: Causative pathogens, antibiotic resistance and therapeutic considerations in acute otitis media. Pediatr Infect Dis J. 1997, 16 (4): 449-456. 10.1097/00006454-199704000-00029.View ArticlePubMed
- Tong HH, Fisher LM, Kosunick GM, Demaria TF: Effect of tumor necrosis factor alpha and interleukin 1-alpha on the adherence of Streptococcus pneumoniae to chinchilla tracheal epithelium. Acta Otolaryngol. 1999, 119 (1): 78-82. 10.1080/00016489950181981.View ArticlePubMed
- Faden H, Duffy L, Foels T, Hong JJ: Adherence of nontypeable Haemophilus influenzae to respiratory epithelium of otitis-prone and normal children. Ann Otol Rhinol Laryngol. 1996, 105 (5): 367-370.View ArticlePubMed
- Zheng CH, Ahmed K, Rikitomi N, Martinez G, Nagatake T: The effects of S-carboxymethylcysteine and N-acetylcysteine on the adherence of Moraxella catarrhalis to human pharyngeal epithelial cells. Microbiol Immunol. 1999, 43 (2): 107-113.View ArticlePubMed
- Zhang JR, Tuomanen E: Molecular and cellular mechanisms for microbial entry into the CNS. J Neurovirol. 1999, 5 (6): 591-603.View ArticlePubMed
- Novotny LA, Jurcisek JA, Pichichero ME, Bakaletz LO: Epitope mapping of the outer membrane protein P5-homologous fimbrin adhesin of nontypeable Haemophilus influenzae. Infect Immun. 2000, 68 (4): 2119-2128. 10.1128/IAI.68.4.2119-2128.2000.PubMed CentralView ArticlePubMed
- Barenkamp SJ, St Geme JW: Identification of a second family of high-molecular-weight adhesion proteins expressed by non-typable Haemophilus influenzae. Mol Microbiol. 1996, 19 (6): 1215-1223.View ArticlePubMed
- Karalus RJ, Murphy TF: Purification and characterization of outer membrane protein P6, a vaccine antigen of non-typeable Haemophilus influenzae. FEMS Immunol Med Microbiol. 1999, 26 (2): 159-166.View ArticlePubMed
- Chen R, Lim JH, Jono H, Gu XX, Kim YS, Basbaum CB, Murphy TF, Li JD: Nontypeable Haemophilus influenzae lipoprotein P6 induces MUC5AC mucin transcription via TLR2-TAK1-dependent p38 MAPK-AP1 and IKKbeta-IkappaBalpha-NF-kappaB signaling pathways. Biochem Biophys Res Commun. 2004, 324 (3): 1087-1094. 10.1016/j.bbrc.2004.09.157.View ArticlePubMed
- Vora P, Youdim A, Thomas LS, Fukata M, Tesfay SY, Lukasek K, Michelsen KS, Wada A, Hirayama T, Arditi M, Abreu MT: Beta-defensin-2 expression is regulated by TLR signaling in intestinal epithelial cells. J Immunol. 2004, 173 (9): 5398-5405.View ArticlePubMed
- Dunne A, O'Neill L: Adaptor usage and Toll-like receptor signaling specificity. FEBS Lett. 2005
- Shuto T, Xu H, Wang B, Han J, Kai H, Gu XX, Murphy TF, Lim DJ, Li JD: Activation of NF-kappa B by nontypeable Hemophilus influenzae is mediated by toll-like receptor 2-TAK1-dependent NIK-IKK alpha /beta-I kappa B alpha and MKK3/6-p38 MAP kinase signaling pathways in epithelial cells. Proc Natl Acad Sci U S A. 2001, 98 (15): 8774-8779. 10.1073/pnas.151236098.PubMed CentralView ArticlePubMed
- Lehrer RI, Lichtenstein AK, Ganz T: Defensins: antimicrobial and cytotoxic peptides of mammalian cells. Annu Rev Immunol. 1993, 11: 105-128. 10.1146/annurev.iy.11.040193.000541.View ArticlePubMed
- Lehrer RI, Ganz T: Antimicrobial peptides in mammalian and insect host defence. Curr Opin Immunol. 1999, 11 (1): 23-27. 10.1016/S0952-7915(99)80005-3.View ArticlePubMed
- Jones DE, Bevins CL: Paneth cells of the human small intestine express an antimicrobial peptide gene. J Biol Chem. 1992, 267 (32): 23216-23225.PubMed
- Jia HP, Schutte BC, Schudy A, Linzmeier R, Guthmiller JM, Johnson GK, Tack BF, Mitros JP, Rosenthal A, Ganz T, McCray PBJ: Discovery of new human beta-defensins using a genomics-based approach. Gene. 2001, 263 (1-2): 211-218. 10.1016/S0378-1119(00)00569-2.View ArticlePubMed
- Linzmeier R, Ho CH, Hoang BV, Ganz T: A 450-kb contig of defensin genes on human chromosome 8p23. Gene. 1999, 233 (1-2): 205-211. 10.1016/S0378-1119(99)00136-5.View ArticlePubMed
- Mc NN, Van R, Tuchin OS, Fleiszig SM: Ocular surface epithelia express mRNA for human beta defensin-2. Exp Eye Res. 1999, 69 (5): 483-490. 10.1006/exer.1999.0722.View Article
- Garcia JR, Krause A, Schulz S, Rodriguez-Jimenez FJ, Kluver E, Adermann K, Forssmann U, Frimpong-Boateng A, Bals R, Forssmann WG: Human beta-defensin 4: a novel inducible peptide with a specific salt-sensitive spectrum of antimicrobial activity. Faseb J. 2001, 15 (10): 1819-1821.PubMed
- Schutte BC, Mitros JP, Bartlett JA, Walters JD, Jia HP, Welsh MJ, Casavant TL, McCray PBJ: Discovery of five conserved beta -defensin gene clusters using a computational search strategy. Proc Natl Acad Sci U S A. 2002, 99 (4): 2129-2133. 10.1073/pnas.042692699.PubMed CentralView ArticlePubMed
- Harder J, Bartels J, Christophers E, Schroder JM: Isolation and characterization of human beta -defensin-3, a novel human inducible peptide antibiotic. J Biol Chem. 2001, 276 (8): 5707-5713. 10.1074/jbc.M008557200.View ArticlePubMed
- Schroder JM, Harder J: Human beta-defensin-2. Int J Biochem Cell Biol. 1999, 31 (6): 645-651. 10.1016/S1357-2725(99)00013-8.View ArticlePubMed
- Singh PK, Jia HP, Wiles K, Hesselberth J, Liu L, Conway BA, Greenberg EP, Valore EV, Welsh MJ, Ganz T, Tack BF, McCray PBJ: Production of beta-defensins by human airway epithelia. Proc Natl Acad Sci U S A. 1998, 95 (25): 14961-14966. 10.1073/pnas.95.25.14961.PubMed CentralView ArticlePubMed
- Lee HY, Andalibi A, Webster P, Moon SK, Teufert K, Kang SH, Li JD, Nagura M, Ganz T, Lim DJ: Antimicrobial activity of innate immune molecules against Streptococcus pneumoniae, Moraxella catarrhalis and nontypeable Haemophilus influenzae. BMC Infect Dis. 2004, 4 (1): 12-10.1186/1471-2334-4-12.PubMed CentralView ArticlePubMed
- Moon SK, Lee HY, Li JD, Nagura M, Kang SH, Chun YM, Linthicum FH, Ganz T, Andalibi A, Lim DJ: Activation of a Src-dependent Raf-MEK1/2-ERK signaling pathway is required for IL-1alpha-induced upregulation of beta-defensin 2 in human middle ear epithelial cells. Biochim Biophys Acta. 2002, 1590 (1-3): 41-51. 10.1016/S0167-4889(02)00196-9.View ArticlePubMed
- O'Neil DA, Porter EM, Elewaut D, Anderson GM, Eckmann L, Ganz T, Kagnoff MF: Expression and regulation of the human beta-defensins hBD-1 and hBD-2 in intestinal epithelium. J Immunol. 1999, 163 (12): 6718-6724.PubMed
- Melhus A, Ryan AF: Expression of cytokine genes during pneumococcal and nontypeable Haemophilus influenzae acute otitis media in the rat. Infect Immun. 2000, 68 (7): 4024-4031. 10.1128/IAI.68.7.4024-4031.2000.PubMed CentralView ArticlePubMed
- Barenkamp SJ, Leininger E: Cloning, expression, and DNA sequence analysis of genes encoding nontypeable Haemophilus influenzae high-molecular-weight surface-exposed proteins related to filamentous hemagglutinin of Bordetella pertussis. Infect Immun. 1992, 60 (4): 1302-1313.PubMed CentralPubMed
- Chun YM, Moon SK, Lee HY, Webster P, Brackmann DE, Rhim JS, Lim DJ: Immortalization of normal adult human middle ear epithelial cells using a retrovirus containing the E6/E7 genes of human papillomavirus type 16. Ann Otol Rhinol Laryngol. 2002, 111 (6): 507-517.View ArticlePubMed
- Watanabe T, Jono H, Han J, Lim DJ, Li JD: Synergistic activation of NF-kappaB by nontypeable Haemophilus influenzae and tumor necrosis factor alpha. Proc Natl Acad Sci U S A. 2004, 101 (10): 3563-3568. 10.1073/pnas.0400557101.PubMed CentralView ArticlePubMed
- Moxon ER: The carrier state: Haemophilus influenzae. J Antimicrob Chemother. 1986, 18 Suppl A: 17-24.PubMed
- Gilsdorf JR: Antigenic diversity and gene polymorphisms in Haemophilus influenzae. Infect Immun. 1998, 66 (11): 5053-5059.PubMed CentralPubMed
- Foxwell AR, Kyd JM, Cripps AW: Nontypeable Haemophilus influenzae: pathogenesis and prevention. Microbiol Mol Biol Rev. 1998, 62 (2): 294-308.PubMed CentralPubMed
- Murphy TF: Haemophilus influenzae in chronic bronchitis. Semin Respir Infect. 2000, 15 (1): 41-51.View ArticlePubMed
- Goodrum KJ, Poulson-Dunlap J: Cytokine responses to group B streptococci induce nitric oxide production in respiratory epithelial cells. Infect Immun. 2002, 70 (1): 49-54. 10.1128/IAI.70.1.49-54.2002.PubMed CentralView ArticlePubMed
- Tsutsumi-Ishii Y, Nagaoka I: Modulation of human beta-defensin-2 transcription in pulmonary epithelial cells by lipopolysaccharide-stimulated mononuclear phagocytes via proinflammatory cytokine production. J Immunol. 2003, 170 (8): 4226-4236.View ArticlePubMed
- Mineshiba J, Myokai F, Mineshiba F, Matsuura K, Nishimura F, Takashiba S: Transcriptional regulation of beta-defensin-2 by lipopolysaccharide in cultured human cervical carcinoma (HeLa) cells. FEMS Immunol Med Microbiol. 2005, 45 (1): 37-44. 10.1016/j.femsim.2005.01.008.View ArticlePubMed
- St Geme JW, Cutter D, Barenkamp SJ: Characterization of the genetic locus encoding Haemophilus influenzae type b surface fibrils. J Bacteriol. 1996, 178 (21): 6281-6287.PubMed CentralPubMed
- Novak R, Charpentier E, Braun JS, Tuomanen E: Signal transduction by a death signal peptide: uncovering the mechanism of bacterial killing by penicillin. Mol Cell. 2000, 5 (1): 49-57. 10.1016/S1097-2765(00)80402-5.View ArticlePubMed
- Tuomanen E, Tomasz A: Induction of autolysis in nongrowing Escherichia coli. J Bacteriol. 1986, 167 (3): 1077-1080.PubMed CentralPubMed
- Kubba H, Pearson JP, Birchall JP: The aetiology of otitis media with effusion: a review. Clin Otolaryngol Allied Sci. 2000, 25 (3): 181-194. 10.1046/j.1365-2273.2000.00350.x.View ArticlePubMed
- DeMaria TF, Prior RB, Briggs BR, Lim DJ, Birck HG: Endotoxin in middle-ear effusions from patients with chronic otitis media with effusion. J Clin Microbiol. 1984, 20 (1): 15-17.PubMed CentralPubMed
- Clemans DL, Bauer RJ, Hanson JA, Hobbs MV, St Geme JW, Marrs CF, Gilsdorf JR: Induction of proinflammatory cytokines from human respiratory epithelial cells after stimulation by nontypeable Haemophilus influenzae. Infect Immun. 2000, 68 (8): 4430-4440. 10.1128/IAI.68.8.4430-4440.2000.PubMed CentralView ArticlePubMed
- Wang B, Cleary PP, Xu H, Li JD: Up-regulation of interleukin-8 by novel small cytoplasmic molecules of nontypeable Haemophilus influenzae via p38 and extracellular signal-regulated kinase pathways. Infect Immun. 2003, 71 (10): 5523-5530. 10.1128/IAI.71.10.5523-5530.2003.PubMed CentralView ArticlePubMed
- Wang B, Lim DJ, Han J, Kim YS, Basbaum CB, Li JD: Novel cytoplasmic proteins of nontypeable Haemophilus influenzae up-regulate human MUC5AC mucin transcription via a positive p38 mitogen-activated protein kinase pathway and a negative phosphoinositide 3-kinase-Akt pathway. J Biol Chem. 2002, 277 (2): 949-957. 10.1074/jbc.M107484200.View ArticlePubMed
- Dinarello CA, Savage N: Interleukin-1 and its receptor. Crit Rev Immunol. 1989, 9 (1): 1-20.PubMed
- Dinarello CA: Biology of interleukin 1. Faseb J. 1988, 2 (2): 108-115.PubMed
- Patel JA, Kunimoto M, Sim TC, Garofalo R, Eliott T, Baron S, Ruuskanen O, Chonmaitree T, Ogra PL, Schmalstieg F: Interleukin-1 alpha mediates the enhanced expression of intercellular adhesion molecule-1 in pulmonary epithelial cells infected with respiratory syncytial virus. Am J Respir Cell Mol Biol. 1995, 13 (5): 602-609.View ArticlePubMed
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/6/12/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.