- Open Access
Augmentation of Pulmonary Epithelial Cell IL-8 Expression and Permeability by Pre-B-cell Colony Enhancing Factor
- Hailong Li†1, 2,
- Peng Liu†1, 2,
- Javier Cepeda1, 2,
- Deyu Fang2, 3,
- R Blaine Easley4,
- Brett A Simon4, 5,
- Li Qin Zhang1, 2 and
- Shui Qing Ye1, 2Email author
© Li et al; licensee BioMed Central Ltd. 2008
- Received: 13 April 2008
- Accepted: 22 September 2008
- Published: 22 September 2008
Previous studies in our lab have identified Pre-B-cell colony enhancing factor (PBEF) as a novel biomarker in acute lung injury (ALI). The molecular mechanism of PBEF involvement in the pathogenesis of ALI is still incompletely understood. This study examined the role of PBEF in regulating pulmonary alveolar epithelial cell IL-8 expression and permeability.
Human pulmonary alveolar epithelial cells (cell line and primary cells) were transfected with human PBEF cDNA or PBEF siRNA and then cultured in the presence or absence of TNFα. PBEF and IL-8 expression were analyzed by RT-PCR and Western blotting. In addition, changes in pulmonary alveolar epithelial and artery endothelial cell barrier regulation with altered PBEF expression was evaluated by an in vitro cell permeability assay.
Our results demonstrated that, in human pulmonary alveolar epithelial cells, the overexpression of PBEF significantly augmented basal and TNFα-stimulated IL-8 secretion by more than 5 to 10-fold and increased cell permeability by >30%; the knockdown of PBEF expression with siRNA significantly inhibited basal and TNFα-stimulated IL-8 secretion by 70% and IL-8 mRNA levels by 74%. Further, the knockdown of PBEF expression also significantly attenuated TNFα-induced cell permeability by 43%. Similar result was observed in human pulmonary artery endothelial cells.
These results suggest that PBEF may play a vital role in basal and TNFα-mediated pulmonary inflammation and pulmonary epithelial barrier dysfunction via its regulation of other inflammatory cytokines such as IL-8, which could in part explain the role of PBEF in the susceptibility and pathogenesis of ALI. These results lend further support to the potential of PBEF to serve as a diagnostic and therapeutic target to ALI.
- A549 Cell
- Acute Lung Injury
- Acute Respiratory Distress Syndrome
- Cell Permeability
- Small Airway Epithelial Cell
Acute lung injury (ALI) is characterized by pulmonary inflammation, non-cardiogenic edema, and severe systemic hypoxemia. Acute respiratory distress syndrome (ARDS) is the severe form of ALI [1, 2]. One of the earliest manifestations of ALI is a diffuse intense inflammatory process and damage to both endothelial and epithelial cell barriers, resulting in marked extravasation of vascular fluid into the alveolar airspace . A number of inflammatory cytokines including tumor necrosis factor-alpha (TNFα) and interleukin 8 (IL-8) can induce or aggravate the inflammation of endothelial and epithelial cells, leading to this barrier dysfunctions . The mortality and morbidity of ALI/ARDS remain high since the etiology and molecular pathogenesis are still incompletely understood.
Our previous study, based on extensive microarray gene expression profiling in canine, murine, and human ALI, revealed pre-B-cell-colony-enhancing factor (PBEF) as a significantly upregulated gene . Analysis of single nucleotide polymorphisms (SNPs) in the PBEF gene proximal promoter region indicated that a GC haplotype had a higher risk of ALI while a TT haplotype may have a lower risk of ALI . Our findings were confirmed and extended by Bajwa et al , who showed that the PBEF T-1001G variant allele and related haplotype are associated with increased odds of developing ARDS and increased hazard of intensive care unit mortality among at-risk patients. In contrast, the C-1543T variant allele and related haplotype are associated with decreased odds of ARDS among patients with septic shock and better outcomes among patients with ARDS. In a mechanistic study, we found that PBEF is critically involved in thrombin-induced lung endothelial cell barrier dysregulation .
The objective of this study was to further elucidate the role of PBEF in pulmonary epithelial cell inflammation and barrier regulation since impaired alveolar epithelial fluid transport is also a characteristic feature in patients with ALI and has been associated with increased morbidity and mortality . Using A549 human pulmonary alveolar epithelial cells and primary bronchial airway epithelial cells, we assessed the effect of PBEF knockdown with PBEF-specific silencing RNA (siRNA) and the effect of PBEF overexpression on TNFα-mediated IL-8 production and on cellular barrier function. Effect of the altered PBEF expression on basal or TNFα stimulated primary human pulmonary artery endothelial cells permeability was also examined to indirectly validate the similar results in the A549 cell line. Study of the role of PBEF in TNFα-mediated pulmonary cell IL-8 production and resultant barrier dysfunctions may help elucidate the molecular mechanisms underlying the role of PBEF in the susceptibility and pathogenesis of ALI.
Rabbit anti-human IL-8 polyclonal antibody (Cat. No. sc-7922, Santa Cruz, California, USA) and mouse anti-human β-actin monoclonal antibody (Cat. No. A1978) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Rabbit anti-human PBEF polyclonal antibody was from Bethyl Laboratories, Inc. (Cat. No. A300-372A, Montgomery, TX, USA). Total mouse lung RNA was from Stratagene (Cat. No. 736511, La Jolla, CA, USA). Recombinant human TNFα (Cat. No. 210-TA) was from R&D Systems Inc. (Minneapolis, MN, USA). Superscript III Reverse Transcriptase (Cat. No. 18080044), Platinum Taq DNA polymerase (Cat. No. 10966018) was from Invitrogen (Carlsbad, CA, USA). Tricine was purchased from the Sigma-Aldrich (Cat. No. T0377, St. Louis, MO, USA). Sources of other key reagents are specified in the relevant text.
Human A549 cells, a lung carcinomatous type II alveolar epithelial cell line, were obtained from ATCC (Cat. No. CCL-185™, Manassas, VA) and maintained in a Dulbecco's Modified Eagle's Medium supplemented with 10% fetal bovine serum, 2 mM glutamine, and penicillin/streptomycin. Primary human lung small airway epithelial cells (Cat. No. CC-2547) were obtained from Lonza (Walkersville, MD, USA) and maintained in a small airway epithelial cell basal medium (Cat. No. CC-3119) with Supplement & Growth factors (Cat. No. CC-4124). Primary human pulmonary artery endothelial cells (HPAEC, Cat. No. CC-2530) were obtained from Cambrex Bio Science Inc. (Walkersville, MD, USA) and maintained in EGM™-2 Endothelial Cell Medium-2 (Cat. No. CC-4176). All cells were cultured at 37°C in a humidified atmosphere of 5% CO2, 95% air. Cells from each primary flask were detached with 0.05% trypsin, resuspended in fresh culture medium, and seeded into 6-well plates for Western blot and RT-PCR analysis or seeded into the culture inserts for in vitro cell permeability assays.
Transfection of PBEF siRNA into human A549 cells, primary human lung small airway epithelial cells and primary HPAEC
PBEF stealth siRNA was designed based on the human PBEF cDNA reference sequence (NM_005746.1) using the BLOCK-iT™ RNAi Designer (Invitrogen, Carlsbad, CA, USA). Using GFP-labeled non-specific siRNA, we first optimized the conditions for human A549 cells transfection and achieved >90% transfection efficiency using the Lipofectamine 2000 reagent (Invitrogen, Carlsbad, CA, USA). To transfect PBEF stealth siRNA into human A549 cells, cells were seeded for 24 h in the regular growth medium (without antibiotics) so that they would be 80–90% confluent at the time of transfection. For each transfection in 24-well plates, 50 pmol PBEF stealth siRNA was diluted in 50 μl Opti-MEM I without serum and gently mixed with 1 μl Lipofectamine 2000 diluted in the 50 μl Opti-MEM I (Invitrogen, Cat. 31985-062). After incubation for 15 min at room temperature, PBEF stealth siRNA and Lipofectamine 2000 complexes were added to each well. Cell culture plates were gently mixed by rocking back and forth. The amount of PBEF stealth siRNA and Lipofectamine 2000 were adjusted according to the different sizes of cell culture plates. Transfected cells were further incubated at 37°C for 24–48 h until treatment with TNFα before intended assays were carried out. Primary human lung small airway epithelial cells were similarly transfected. Transfection of PBEF siRNA into HPAEC was performed as previously described by Ye et al .
Preparation and expression of the PBEF-overexpressing construct pCAGGS-hPBEF
A human PBEF (hPBEF) coding cDNA was amplified from A549 cell total RNA by RT-PCR using the following primer pair designed according to the reference human PBEF mRNA sequence (NM_005746.2): forward primer, 5'-TTAGAATTC GCCACC ATGCCTGCGGCAGAAGCC-3'and reverse primer, 5'-TTAGAATTC TTAATGGTGATGGTGATGATG CAAATGATGTGCTGCTTCCAGTTC-3'. The regular bold letters indicate the optimized Kozac sequence. The bold italic letter part is His tag sequence. The underlined sequences are EcoRI adaptors. The amplified human PBEF cDNA was digested with EcoRI and subcloned into the unique EcoRI site of pCAGGS vector, which was provided by Dr. Deyu Fang (Department of Molecular Microbiology and Immunology, University of Missouri-Columbia). After the cloning, pCAGGS-hPBEF was sequence-verified. In this construct, human PBEF expression was driven by a chicken beta-actin/rabbit beta-globin hybrid promoter (AG) with an enhancer from the human cytomegalovirus immediate early promoter (CMV-IE). Overexpression of PBEF in A549 cells and HPAEC was carried out by a transient transfection of pCAGGS-hPBEF. Briefly, one day before transfection, A549 cells or HPAEC were plated in 6-well plate at 5 × 105 cells/well in 2 ml of growth medium without antibiotics. On the day of transfection, cells were at 95% confluence. For each well, 4 μg plasmid DNA was transfected using Lipofectamine 2000 according to the suppliers' instruction. Cell medium and cell lysate proteins were harvested at 48, 72 and 96 hours after the transfection for western blotting analyses of IL-8, PBEF and β-actin protein levels in A549 cells. pCAGGS-hPBEF or pCAGGS transfected HPAEC were used only for the assessment of cell permeability.
Isolation of RNA and RT-PCR analysis
Primers and products sizes
Western blot analysis was performed following the protocol of Bio-Rad Company. Briefly, after washing with PBS, cells were lysed with 500 μl of cell lysis buffer containing 10 mM Tris (pH 7.4), 1% Triton X-100, 0.5% Nonidet P-40, 150 mM NaCl, 1 mM EDTA, 0.2 mM EGTA, 0.2 mM vanadate, 0.2 mM PMSF, and 0.5% protease inhibitor cocktail. Total cell lysates were cleared by centrifugation and boiled with the same amount of 4× SDS sample buffer for 5 min. Total protein of cell lysates was quantified using the BCA Protein Assay Kit (Pierce Biotechnology, Inc., Rockford, IL, USA). An equal amount of total protein from each sample was then subjected to 16.5% Tris/tricine polyacrylamide gel electrophoresis. The separated proteins were transferred to PVDF membranes by electrotransfer. The blots were subsequently blocked with 5% bovine serum albumin in PBS containing 0.1% Tween 20 (TBS-T) at room temperature for 1 h and then incubated at 4°C overnight with primary antibodies of interest. After washing three times for 10 min with TBS-T, the membrane was incubated with horseradish-peroxidase-linked secondary antibodies of interest at room temperature for 1 h. The blots were then visualized with the ECL Western blot detection system (Cat. No. RPN2106, Amersham Bosciences, Buckinghamshire, UK). The same membrane was re-probed with an anti-human β-actin antibody. β-actin was used as an internal control. Band density on Western blot images was used as a measure of assayed protein level. The band image was acquired using an Alpha Imager and analyzed by the AlphaEase™ Stand Alone Software.
In Vitro Cell Permeability Assay
In Vitro Cell Permeability Assay was carried out according to the protocol of the CHEMICON in vitro Vascular Permeability Assay kit (Cat. No. ECM640, Millipore, Billerica, MA, USA). Briefly, cells were seeded to the culture inserts of permeability chambers (1.0 × 106 cells/ml) that were coated with collagen. Then, cells were incubated in 37°C and 5% until a monolayer was formed. After TNFα (Cat. No. 636-R1, R&D systems, Minneapolis, MN, USA) was added, cells were incubated for another 18 hours at 37°C and 5% CO2 in the tissue culture incubator. Finally, 150 μl of FITC-Dextran was added to each insert for 5 min at room temperature, and then 100 μl of the solution in the bottom chamber was transferred to a 96-well plate. The plate was read in a TriStar Multimode Reader (LB 941, Berthold Technologies GnbH & Co. KG, Bad Wildbad, Germany) at wavelengths of 485 and 530 nm. Reagent control wells were treated with basal medium and growth medium only. Blank inserts without cells plated were also included as controls.
Statistical analyses were performed using SigmaStat (ver 3.5, Systat Software, Inc., San Jose, CA, USA). Results are expressed as mean ± standard deviation (SD) of four samples from at least two independent experiments. Stimulated samples were compared with controls by unpaired Student's t test. P < 0.05 was considered statistically significant.
Dose-response and time-course of TNFα induced IL-8 protein expression in A549 cells
Dose-response and time-course of TNFα induced PBEF protein expression in A549 cells
TNFα induction of IL-8 and PBEF expression at their mRNA levels in A549 cells
Knockdown of PBEF protein and mRNA expression by PBEF stealth siRNA in A549 cells
PBEF silencing attenuated TNFα-induced increases in IL-8 secretion and IL-8 mRNA expression within A549 cells
PBEF silencing attenuated TNFα-induced increases in IL-8 secretion and PBEF protein expression in lung primary small airway epithelial cells
To further confirm the above results, we also investigated PBEF effects on TNFα-induced IL-8 secretion in primary human lung small airway epithelial cells. In Figure 5 (panels E and F), PBEF silencing is shown to decrease IL-8 secretion in TNFα-stimulated conditions (siRNA vs. control: 10609.50 ± 4086.65 vs. 28801.42 ± 1235.48, n = 4, p < 0.01). In contrast, scRNA demonstrated no difference from control. These results indicate that PBEF is also involved in IL-8 expression and secretion in TNFα induced conditions in primary human lung small airway epithelial cells.
PBEF over-expression augmented IL-8 secretion from A549 cells
PBEF expression affected cell permeability in A549 cells and human pulmonary artery endothelial cells (HPAEC)
Our findings demonstrate that the modulation of PBEF expression resulted in parallel changes in TNFα-mediated IL-8 production and secretion as well as alveolar epithelial cell permeability. These results provide new insight into the role of PBEF in the inflammatory pathways and functional abnormalities associated with ALI.
There is considerable experimental and clinical evidence that pro-inflammatory cytokines play a major role in the pathogenesis of ALI/ARDS from inflammatory causes, such as sepsis, pneumonia, aspiration, and shock , as well as from mechanical stress [9–11]. The landmark ARDSnet clinical trial found that a lung-protective ventilatory strategy reduces mortality by 22% in patients with ALI, a result that in part may be ascribed to the marked reduction in the concentration of pro-inflammatory cytokines released into the airspaces of the injured lung [12, 8]. TNFα and IL-8 are among important early mediators of ALI . It has been shown that TNFα is present in increased amounts in the bronchoalveolar lavage fluid (BALF) of patients with ARDS , in the serum during the onset of sepsis-induced lung injury , and acutely increases in both serum and BALF when changing from a lung protective to non-protective ventilation strategy . Increasing TNFα biological activity has been demonstrated over the first week of ARDS and there are direct relationships between the molar ratio of TNFα/soluble TNF-receptor in the BALF and severity of ALI (lung compliance and severity of hypoxemia) . The role of TNFα in pulmonary pathophysiology has been well studied, and includes induction of cellular inflammatory reactions, enhancement of oxidative stress, and increased expression of various proinflammatory molecules .
Among the TNFα induced pro-inflammatory cytokines, IL-8 is regarded as one of the most important mediators in the pathogenesis of ARDS. In BALF, IL-8 levels were significantly increased in patients with ARDS and correlated with the development of ARDS in at-risk patients [16, 17]. IL-8 has been identified as one of biomarkers of ALI/ARDS mortality . In fact, IL-8 was first purified and molecularly cloned as a neutrophil chemotactic factor from lipopolysaccharide-stimulated human mononuclear cell supernatants . Since then, studies of models of acute inflammation have established IL-8 as a key mediator in neutrophil mediated acute inflammation . In acid aspiration- and endotoxemia-induced ARDS in rabbits, IL-8 is produced in the lungs [21, 22]. In both models, the abrogation of IL-8 activity reduces neutrophil infiltration as well as tissue damage. It was demonstrated that TNFα mediated IL-8 production can suppress neutrophil apoptosis  and thus potentially prolong neutrophil migration into the lungs and damage to lung tissues, including alveolar epithelial barrier function .
Our data in this study indicate that TNFα significantly induces PBEF expression at both the mRNA and protein levels in A549 cells (Figures 2, 3, 4, 5), suggesting that PBEF may be an intermediate target of TNFα involved in the inflammatory process during the pathogenesis of ALI. The knockdown of PBEF expression by PBEF siRNA significantly blunted TNFα-stimulated IL-8 secretion and its production in A549 cells (Figures 6, 7), and PBEF-overexpression augmented IL-8 secretion from A549 cell (Figure 7). These results support the concept that PBEF may be an inflammatory signal transducer of TNFα or other inflammatory stimuli to regulate the synthesis of IL-8 or other inflammatory cytokines. These conclusions can be corroborated by evidence in non-lung tissue studies. PBEF silencing has been shown to prevent the suppression of neutrophil apoptosis caused by TNFα, IL-8 and other mediators . In addition, PBEF gene expression is up-regulated in severely infected fetal membranes . Inflammatory stimuli in fetal membranes inducing NF-κB and AP-1 have been shown to up-regulate PBEF . The recombinant human PBEF treatment of amnion-like epithelial cells and fetal membrane explants significantly increased IL-6 and IL-8 expression . Considered together, PBEF could play a critical role as an inflammatory cytokine during the pathogenesis of ALI.
Both endothelial and epithelial injuries were observed in earlier ultrastructural studies of the lung in patients dying with ALI secondary to sepsis [29, 30]. Increased vascular permeability and endothelial injury contribute to the profound pathophysiological derangements in ALI [31, 32]. If the alveolar epithelium is also damaged, the change in both endothelial and epithelial permeability could lead to major alveolar flooding with high-molecular-weight proteins, with prolonged changes in gas exchange, altered compliance and a much higher likelihood of disordered repair . Normally, the lung alveolar epithelium forms an extremely tight barrier that restricts the movement of proteins and liquid from the interstitium into the alveolar spaces. In ALI, impaired alveolar epithelial function in the lungs is a marker of poor outcome in ALI . A number of inflammatory cytokines, including TNFα and IL-8, can induce or aggravate the inflammation of endothelial and epithelial cells, leading to their barrier dysfunctions . In this study we have demonstrated (Figure 7) that the TNFα stimulated increased in A549 cell permeability is significantly attenuated by the knockdown of PBEF expression by PBEF siRNA. Overexpression of PBEF increased A549 cell permeability in both basal and TNFα induced conditions. These results suggest that PBEF may have an important role in epithelial cell barrier regulation. A549 cells are an alveolar Type II tumor epithelial cell line. While the type II epithelial cell only covers 7% of the alveolar surface area, it constitutes 67% of the epithelial cell number within the alveoli , pointing to its biochemical importance. The permeability increase of A549 cells in the TNFα-stimulated condition involves both paracellular permeability, with gap formation visualized by actin cytoskeleton staining, and basement membrane permeability . Since A549 cells usually do not form a regular monolayer, we went to examine whether a similar effect can be observed in a primary HPAEC, which forms a typical monolayer. Indeed, we found that PBEF expression similarly affected the HPAEC permeability (Figure 7).
While an overexpression of PBEF results in an increased basal permeability, knocking down PBEF expression failed to alter the basal permeability both in A549 cells and HPAEC. It is possible that in our study, transfection of pCAGGS-PBEF engendered at least 3 fold higher PBEF protein expression, but transfection of PBEF siRNA only resulted in about 60% decrease of PBEF level, which might explain the subdued effect of the latter in the basal level. TNFα mediated effect may be partly due to its induction of IL-8 production. IL-8 has been demonstrated to induce actin fiber rearrangement and intercellular gap formation in endothelial cells . IL-8 could have a similar effect on epithelial barrier function. Our previous study found that reductions in PBEF protein expression significantly attenuated endothelial barrier dysfunction induced by the potent edemagenic agent, thrombin, reflected by reductions in transendothelial electric resistance . Furthermore, reductions in PBEF protein expression blunted thrombin-mediated increases in Ca2+ entry, polymerized actin formation, and myosin light chain phosphorylation , events critical to the thrombin-mediated permeability response . Whether similar mechanisms account for the attenuating effects of PBEF knockdown on TNFα-induced epithelial and endothelial cell barrier dysfunction remains to be elucidated in future studies.
In summary, this study demonstrated that TNFα significantly induced PBEF and IL-8 expression at both the mRNA and protein levels in A549 cells. PBEF-overexpression augmented IL-8 secretion and epithelial cell permeability in A549 cells, and the knockdown of PBEF expression by PBEF siRNA significantly blunted TNFα-stimulated IL-8 secretion and mRNA production and attenuated TNFα-induced cell permeability of A549 cells. Since inflammation and increased permeability is a hallmark of the pathogenesis of ALI, these results suggest that PBEF may play a critical role as an inflammatory cytokine in the dysregulation of alveolar epithelial cell barriers in the pathogenesis of ALI. These results lend further support to the potential of PBEF to serve as a diagnostic and therapeutic target in future studies of lung injury.
This work was in part supported by NHLBI/NIH Grants 1R01HL080042-01A1 (Ye, S.Q.) and HL073994 (Simon, B.A.), a Foundation for Anesthesia Education and Research Mentored Research Training Grant (Easley, R.B.), and the University of Missouri start-up fund (Ye, S.Q.).
- Wheeler AP, Bernard GR: Acute lung injury and the acute respiratory distress syndrome: a clinical review. Lancet. 2007, 1553-64. 10.1016/S0140-6736(07)60604-7. 9572Google Scholar
- Calfee CS, Matthay MA: Nonventilatory treatments for acute lung injury and ARDS. Chest. 2007, 131 (3): 913-920. 10.1378/chest.06-1743.PubMedPubMed CentralView ArticleGoogle Scholar
- Matthay MA, Zimmerman GA, Esmon C, Bhattacharya J, Coller B, Doerschuk CM, Floros J, Gimbrone MA, Hoffman E, Hubmayr RD: Future research directions in acute lung injury: summary of a National Heart, Lung, and Blood Institute working group. Am J Respir Crit Care Med. 2003, 167: 1027-1035. 10.1164/rccm.200208-966WS.PubMedView ArticleGoogle Scholar
- Frank JA, Parsons PE, Matthay MA: Pathogenetic significance of biological markers of ventilator-associated lung injury in experimental and clinical studies. Chest. 2006, 130 (6): 1906-14. 10.1378/chest.130.6.1906.PubMedPubMed CentralView ArticleGoogle Scholar
- Ye SQ, Simon B, Maloney JP, Zambelli-Weiner A, Gao L, Grant A, Easley RB, McVerry B, Tuder RM, Standiford T, Brower R, Barnes K, Garcia JG: Pre-B-cell colony-enhancing factor as a potential novel biomarker in acute lung injury. Am J Respir Crit Care Med. 2005, 171 (4): 361-370. 10.1164/rccm.200404-563OC.PubMedView ArticleGoogle Scholar
- Bajwa EK, Yu CL, Gong MN, Thompson BT, Christiani DC: Pre-B-cell colony-enhancing factor gene polymorphisms and risk of acute respiratory distress syndrome. Crit Care Med. 2007, 35: 1290-1295. 10.1097/01.CCM.0000260243.22758.4F.PubMedView ArticleGoogle Scholar
- Ye SQ, Zhang LQ, Adyshev D, Usatyuk PV, Garcia AN, Lavoie TL, Verin AD, Natarajan V, Garcia JG: Pre-B-cell-colony-enhancing factor is critically involved in thrombin-induced lung endothelial cell barrier dysregulation. Microvasc Res. 2005, 70 (3): 142-51. 10.1016/j.mvr.2005.08.003.PubMedView ArticleGoogle Scholar
- Parsons PE, Matthay MA, Ware LB, Eisner MD, National Heart, Lung, Blood Institute Acute Respiratory Distress Syndrome Clinical Trials Network: Elevated plasma levels of soluble TNF receptors are associated with morbidity and mortality in patients with acute lung injury. Am J Physiol Lung Cell Mol Physiol. 2005, 288 (3): L426-31. 10.1152/ajplung.00302.2004.PubMedView ArticleGoogle Scholar
- Stüber F, Wrigge H, Schroeder S, Wetegrove S, Zinserling J, Hoeft A, Putensen C: Kinetic and reversibility of mechanical ventilation-associated pulmonary and systemic inflammatory response in patients with acute lung injury. Intensive Care Med. 2002, 28 (7): 834-41. 10.1007/s00134-002-1321-7.PubMedView ArticleGoogle Scholar
- Parsons PE, Eisner MD, Thompson BT, Matthay MA, Ancukiewicz M, Bernard GR: Lower tidal volume ventilation and plasma cytokine markers of inflammation in patients with acute lung injury. Crit Care Med. 2005, 33: 1-6. 10.1097/01.CCM.0000149854.61192.DC.PubMedView ArticleGoogle Scholar
- Ranieri VM, Suter PM, Tortorella C, De Tullio R, Dayer JM, Brienza A, Bruno F, Slutsky AS: Effect of mechanical ventilation on inflammatory mediators in patients with acute respiratory distress syndrome: a randomized controlled trial. JAMA. 1999, 282 (1): 54-61. 10.1001/jama.282.1.54.PubMedView ArticleGoogle Scholar
- Parsons PE, Eisner MD, Thompson BT, Matthay MA, Ancukiewicz M, Bernard GR, Wheeler AP, NHLBI Acute Respiratory Distress Syndrome Clinical Trials Network: Lower tidal volume ventilation and plasma cytokine markers of inflammation in patients with acute lung injury. Crit Care Med. 2005, 33 (1): 1-6. 10.1097/01.CCM.0000149854.61192.DC.PubMedView ArticleGoogle Scholar
- Park WY, Goodman RB, Steinberg KP, Ruzinski JT, Radella F, Park DR, Pugin J, Skerrett SJ, Hudson LD, Martin TR: Cytokine balance in the lungs of patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2001, 164: 1896-1903.PubMedView ArticleGoogle Scholar
- Korcheva V, Wong J, Lindauer M, Jacoby DB, Iordanov MS, Magun B: Role of apoptotic signaling pathways in regulation of inflammatory responses to ricin in primary murine macrophages. Mol Immunol. 2007, 44 (10): 2761-71. 10.1016/j.molimm.2006.10.025.PubMedPubMed CentralView ArticleGoogle Scholar
- Mukhopadhyay S, Hoidal JR, Mukherjee TK: Intravenous administration of activated protein C in Pseudomonas-induced lung injury: impact on lung fluid balance and the inflammatory response. Respir Res. 2006, 11 (7): 125-10.1186/1465-9921-7-125.View ArticleGoogle Scholar
- Adams JM, Hauser CJ, Livingston DH, Lavery RF, Fekete Z, Deitch EA: Early trauma polymorphonuclear neutrophil responses to chemokines are associated with development of sepsis, pneumonia, and organ failure. J Trauma. 2001, 51: 452-456.PubMedView ArticleGoogle Scholar
- Hudson LD: Causes of the adult respiratory di stress syndrome – clinical recognition. Clin Chest Med. 1982, 3: 195-212.PubMedGoogle Scholar
- Ware LB: Prognostic determinants of acute respiratory distress syndrome in adults: impact on clinical trial design. Crit Care Med. 2005, 33 (3 Suppl): 217-222. 10.1097/01.CCM.0000155788.39101.7E.View ArticleGoogle Scholar
- Matsushima K, Morishita K, Yoshimura T, Lavu S, Kobayashi Y, Lew W, Appella E, Kung HF, Leonard EJ, Oppenheim JJ: Molecular cloning of a human monocyte-derived neutrophil chemotactic factor (MDNCF) and the induction of MDNCF mRNA by interleukin 1 and tumor necrosis factor. J Exp Med. 1988, 167 (6): 1883-93. 10.1084/jem.167.6.1883.PubMedView ArticleGoogle Scholar
- Mukaida N: Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases. Am J Physiol Lung Cell Mol Physiol. 2003, 284 (4): L566-L577.PubMedView ArticleGoogle Scholar
- Folkesson HG, Matthay MA, Hebert CA, Broaddus VC: Acid aspiration-induced lung injury in rabbits is mediated by interleukin-8-dependent mechanisms. J Clin Invest. 1995, 96: 107-116. 10.1172/JCI118009.PubMedPubMed CentralView ArticleGoogle Scholar
- Yokoi K, Mukaida N, Harada A, Watanabe Y, Matsushima K: Prevention of endotoxemia-induced acute respiratory distress syndrome-like lung injury in rabbits by a monoclonal antibody to IL-8. Lab Invest. 1997, 76: 375-384.PubMedGoogle Scholar
- Dunican AL, Leuenroth SJ, Grutkoski P, Ayala A, Simms HH: TNFalpha-induced suppression of PMN apoptosis is mediated through interleukin-8 production. Shock. 2000, 14: 284-288.PubMedView ArticleGoogle Scholar
- Modelska K, Pittet JF, Folkesson HG, Courtney V, Matthay MA: Acid-induced lung injury. Protective effect of anti-interleukin-8 pretreatment on alveolar epithelial barrier function in rabbits. Am J Respir Crit Care Med. 1999, 160: 1450-1456.PubMedView ArticleGoogle Scholar
- Jia SH, Li Y, Parodo J, Kapus A, Fan L, Rotstein OD, Marshall JC: Pre-B cell colony-enhancing factor inhibits neutrophil apoptosis in experimental inflammation and clinical sepsis. J Clin Invest. 2004, 113 (9): 1318-27.PubMedPubMed CentralView ArticleGoogle Scholar
- Ognjanovic S, Bao S, Yamamoto SY, Garibay-Tupas J, Samal B, Bryant-Greenwood GD: Genomic organization of the gene coding for human pre-B-cell colony enhancing factor and expression in human fetal membranes. J Mol Endocrinol. 2001, 26: 107-117. 10.1677/jme.0.0260107.PubMedView ArticleGoogle Scholar
- Kendal CE, Bryant-Greenwood GD: Pre-B-cell colony-enhancing factor (PBEF/Visfatin) gene expression is modulated by NF-kappaB and AP-1 in human amniotic epithelial cells. Placenta. 2007, 28 (4): 305-14. 10.1016/j.placenta.2006.03.011.PubMedView ArticleGoogle Scholar
- Ognjanovic S, Bryant-Greenwood GD: Pre-B-cell colony-enhancing factor, a novel cytokine of human fetal membranes. Am J Obstet Gynecol. 2002, 187 (4): 1051-1058. 10.1067/mob.2002.126295.PubMedView ArticleGoogle Scholar
- Bachofen A, Weibel ER: Alterations of the gas exchange apparatus in adult respiratory insufficiency associated with septicemia. Am Rev Respir Dis. 1977, 116: 589-615.PubMedView ArticleGoogle Scholar
- Bachofen M, Weibel ER: Structural alterations of lung parenchyma in the adult respiratory distress syndrome. Clin Chest Med. 1982, 3: 35-56.PubMedGoogle Scholar
- Bachofen H, Bachofen M, Weibel ER: Ultrastructural aspects of pulmonary edema. J Thorac Imaging. 1988, 3 (3): 1-7. 10.1097/00005382-198807000-00005.PubMedView ArticleGoogle Scholar
- Dudek SM, Garcia JG: Cytoskeletal regulation of pulmonary vascular permeability. J Appl Physiol. 2001, 91 (4): 1487-500.PubMedGoogle Scholar
- Liener UC, Brückner UB, Knöferl MW, Steinbach G, Kinzl L, Gebhard F: Chemokine activation within 24 hours after blunt accident trauma. Shock. 2000, 17 (3): 169-172. 10.1097/00024382-200203000-00002.View ArticleGoogle Scholar
- Parsons PE, Eisner MD, Thompson BT, Matthay MA, Ancukiewicz M, Bernard GR: Lower tidal volume ventilation and plasma cytokine markers of inflammation in patients with acute lung injury. Crit Care Med. 2005, 33: 1-6. 10.1097/01.CCM.0000149854.61192.DC.PubMedView ArticleGoogle Scholar
- Thomas R, Martin NH, Morio N, Gustavo MB: Apoptosis and epithelial injury in the lungs. The Proceedings of the American Thoracic Society. 2005, 2: 214-220. 10.1513/pats.200504-031AC.View ArticleGoogle Scholar
- Leone AK, Chun JA, Koehler CL, Caranto J, King JM: Effect of proinflammatory cytokines, tumor necrosis factor-alpha and interferon-gamma on epithelial barrier function and matrix metalloproteinase-9 in Madin Darby canine kidney cells. Cell Physiol Biochem. 2007, 19 (1–4): 99-112. 10.1159/000099198.PubMedView ArticleGoogle Scholar
- Crapo JD, Barry BE, Gehr P: Cell number and cell characteristics of the normal human lung. Am Rev Respir Dis. 1982, 126: 332-337.PubMedGoogle Scholar
- Lacherade JC, Van LA, Planus E, Escudier E, D'Ortho MP, Lafuma C, Harf A, Delclaux C: Evaluation of basement membrane degradation during TNF-alpha-induced increase in epithelial permeability. Am J Physiol Lung Cell Mol Physiol. 2001, 281 (1): L134-143.PubMedGoogle Scholar
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.