- Research article
- Open Access
Chronic activation of the epithelial immune system of the fruit fly's salivary glands has a negative effect on organismal growth and induces a peculiar set of target genes
© Abdelsadik and Roeder; licensee BioMed Central Ltd. 2010
- Received: 3 November 2009
- Accepted: 26 April 2010
- Published: 26 April 2010
Epithelial and especially mucosal immunity represents the first line of defence against the plethora of potential pathogens trying to invade via the gastrointestinal tract. The salivary glands of the fruit fly are an indispensable part of the gastrointestinal tract, but their contribution to the mucosal immunity has almost completely been neglected. Our major goal was to elucidate if the fly's salivary glands are able to mount an immune response and what the major characteristics of this immune response are.
Ectopic activation of the IMD-pathway within the salivary gland cells is able to induce an immune response, indicating that the salivary glands are indeed immune competent. This reaction is characterized by the concurrent expression of numerous antimicrobial peptide genes. In addition, ectopic activation of the salivary gland's immune response induces morphological changes such as dwarfism throughout all developmental stages and a significantly decreased length of the salivary glands themselves. DNA-microarray analyses of the reaction revealed a complex pattern of up- and downregulated genes. Gene ontology analyses of regulated genes revealed a significant increase in genes associated with ribosomal and proteasomal function. On the other hand, genes coding for peptide receptors and some potassium channels are downregulated. In addition, the comparison of the transcriptional events induced following IMD-activation in the trachea and the salivary glands shows also only a small overlap, indicating that the general IMD-activated core transcriptome is rather small and that the tissue specific component of this response is dominating. Among the regulated genes, those that code for signaling associated protease activity are significantly modulated.
The salivary glands are immune-competent and they contribute to the overall intestinal immune system. Although they produce antimicrobial peptides, their overall response is highly tissue-specific. Our analysis indicates that chronic activation of the salivary gland's immune system is costly, as it induces severe reduction in growth throughout development. The IMD-regulated increase in expression levels of the fly's presenilin representatives opens the opportunity to use the salivary glands for studying the physiological and pathophysiological role of these genes in a simple but functional environment.
- Salivary Gland
- Antimicrobial Peptide
- Downregulated Gene
- Autophagic Cell Death
- Ectopic Activation
The immune system is indispensable for multicellular organisms to cope with different pathogens such as bacteria, viruses or fungi. Most animals solely rely on their innate immune system that utilizes phagocytosis, encapsulation, or antimicrobial peptides among many other strategies[1, 2]. Even in vertebrates, where it functions as a first line of defence, it is indispensable for normal life. Interest in innate immunity was revitalized by the identification of Toll-receptors in Drosophila and since then the fly has served as one of its most informative models . The phylogenetically most ancient type of innate immune systems, the epithelial immunity, has almost completely been overlooked. Epithelial cells, including those of the airways and the intestine, as the most important ones, are able to launch a protective, antimicrobial response if confronted with pathogens. Most notably, both epithelia react with expression of antimicrobial peptide genes [5, 6]. The intestinal immune system is in a special position, because it not only has to fight pathogens, but at the same time, it has to protect the endogenous microbiota. Thus, holding a homeostatic balance between tolerance and profound immune responses is the most important regulatory task of the intestinal immune system. Deregulation of this homeostatic equilibrium might end up into chronic inflammatory diseases of the epithelium, such as Crohn's disease and ulcerative colitis. In Drosophila, a wealth of information regarding the architecture of innate immune systems has accumulated over the last decade. Although most studies focussed on the systemic immune response, some information regarding epithelial immunity, especially about intestinal immunity were generated. In Drosophila, only two signalling pathways converge onto activation of NF-κB factors, the Toll- and the IMD-pathway . Now, it is common knowledge that epithelial immune responses in the fly rely on the IMD-pathway. We have shown that, at least in the airway epithelium, the inability of the Toll-pathway to function properly, is due to the lack of vital pathway members . Nevertheless, it has to be mentioned that other pathways, not directly converging onto NF-κB activation, such as the JNK- or the JAK/STAT-pathway are operative in epithelial immunity [8, 9].
In the intestinal epithelium, two major response types have been reported following pathogen challenge. These reactions are the release of antimicrobial peptides and the production of reactive oxygen species [10–13]. The intestine's function in Drosophila is to digest microbe-rich food such as decaying fruits while protecting the fly from infections. Expression of AMPs is enhanced by activation of the IMD pathway and provides a partial protection against entomopathogenic bacteria such as Pseudomonas entomophila. Another arm of the immune response that complements the IMD response of AMP genes is the production of reactive oxygen species (ROS). Apparently, this system is sufficient to cope with most pathogens[10, 11]. IMD-mediated response of AMP-genes seems to be a back up system to control ROS-response against pathogens[12, 13].
In general, the intestinal epithelium appears to be refractory towards pathogen confrontation, presumably due to the presence of inhibitory signals, either those that digest peptidoglycans as the most important pathogen associated molecular patterns (PAMPs) or those that repress IMD-mediated expression[15, 16]. Taken together, regulation of antimicrobial responses in the intestinal epithelium appears to be a complex network including activation and inhibition at different levels [17–19].
Another part of the digestive system that may have the potential to mount an immune response has largely been overlooked, the salivary glands. Salivary glands are an integral part of the intestinal tract, often enabling the uptake and transport of ingested material into the digestive tract. They are the gatekeepers of the intestinal system, being essential for various aspects of the intestine's immunity. Drosophila salivary glands consist of two major cell types: secretory cells that synthesize and secrete high levels of protein and duct cells that form the simple tubes connecting the secretory cells to the larval mouth. Salivary glands differentiate without further cell division and increase in size simply by increasing the volume of individual cells. In recent studies, salivary glands served as a model to study aspects of relevant for organogenesis and the role of various different genes in this process [20–22]. Here we show that salivary glands can mount a protective immune response that is characterized by the expression of antimicrobial peptide genes. Using ectopic expression of the pgrp-l c gene, a procedure, which has already been shown to activate innate immune responses in the fly [23, 24], we specifically activate the immune response of the salivary glands. Fly larvae experiencing a sustained activation of their salivary gland IMD-pathway show a pronounced phenotype that is characterized by reduced overall size of the organ and reduced size of the flies. In addition to various antimicrobial peptide genes, expression of numerous other genes with relevance for signalling, including proteases with signalling activities such as presenilin or signal peptide peptidase is regulated in this organ.
Targeted expression of PGRPs was shown to be sufficient for activation of the IMD-pathway, one major arm of the fly's innate immune system. It enables immune activation without any contact to pathogens in a spatially restricted manner, in those tissues that are immune competent. We used two different effector lines, enabling either production of the membrane protein PGRP-LC or of the soluble receptor PGRP-LE. Ectopic production of PGRP-LC is expected to induce a cell-autonomous immune response, whereas that of PGRP-LE is expected to induce an organ-wide or even systemic response (Fig. 1B). In initial experiments, it became apparent that ectopic expression of the pgrp-le gene in the salivary glands only induces activation also in other parts of the intestinal system (Fig. 1C), indicating that it acts as an organ-wide activator. In contrast, the primary effects of pgrp-lc expression remain restricted to the salivary glands. All following experiments were performed with the pgrp-lc construct allowing to focus on the effects of IMD-pathway activation in the salivary glands only.
Gene ontology analysis using the Fatigo program package  revealed significant peculiarties of both, the up- and downregulated genes in the larval salivary glands following activation of the IMD-pathway (Fig. 4A). GO ontology analysis in comparison with all Drosophila genes revealed that some functional groups are significantly enriched in the cohort of upregulated genes. Most significantly is the clustering of gene products associated with ribonucleoprotein complexes, the proteasome and with cation transporter activities. KEGG pathway analysis of these genes revealed a significant enrichment of the oxidative phosphorylation pathway (Fig. 4A, top, additional file 1). The cohort of downregulated genes shows a clustering of genes associated with peptide receptor activity and alkali metal ion binding (Fig 4A, bottom, additional file 1). 24 ribosomal proteins in total are among the upregulated genes in the salivary glands and 7 genes coding for proteasome subunits. Regarding the downregulated genes, peptide receptor coding genes are conspicuous. In addition to allatostatin receptors, a tachykinin-like, a SIFamide and a gonadotropin-releasing hormone receptor are downregulated (additional file 1). In the group of alkali metal ion binding, ion channels, especially potassium channels are present (such as shaker b and ether a go-go).
A more detailed analysis of cohorts of regulated genes revealed only a minor overlap with the canonical set of immune genes set up in the Lemaitre lab http://www.cnrs-gif.fr/cgm/immunity/index_gb.html (Fig. 4B, C). This comprehensive list is a compilation of genes identified in whole genome wide infection studies  and bioinformatics analysis of Drosophila genes. Only 11 genes in the upregulated and 18 genes in the downregulated cohort are classified as immune genes, meaning that just 2-5% of all regulated genes fall into this category. Based on Venn-diagram analysis, we compared the cohort of upregulated genes with those upregulated following an experimental infection with the insect pathogen Erwinia carotovora either in the trachea or the gut [9, 27](Fig. 4B). Overlaps are also not high with 15 genes in common between Salivary glands upregulated and either the tracheal or the gut infection upregulated cohorts (Fig. 4B, additional file 2).
Using a similar experimental approach, i.e. ectopic activation of the epithelial immune system through expression of the pgrp-lc gene, we identified the regulated transcriptomes in the larval airway epithelium, the trachea. For these experiments, animals with the same genetic background, which are of the same age, and were held under identical conditions, were used . The overlaps in the cohorts of regulated genes are slightly larger (22) (Fig. 4C). Thus, these experiments indicate that NF-kB dependent gene expression is highly context-dependent, meaning that different tissues activate largely different sets of genes if the IMD-pathway is activated ectopically. In addition, a total of 31 genes are shared with the set of genes identified as involved in susceptibility to gut infections  (Additional files 3 and 4. Larval salivary glands are an exquisite model for studying the molecular basis of autophagic cell death. In the experimental flies, we found no histological signs of autophagic cell death. In addition, we only found very few genes that are usually associated with autophagic cell death to be regulated (up: maf-s, rab-7. Obp-99, elf-5A, cyclophilin-1, CG10992, CG9760; down: comm3). This finding is in-line with earlier observations that NF-kB activation is not necessary for cell death of salivary glands, thus excluding confounding influences from factors related to autophagy in the salivary glands .
The salivary glands of the fly are an important part of the digestive tract and thus should contribute to the immune response of the entire organ. In addition, salivary gland function is indispensable for normal life, making it necessary to protect this organ. A partial protection is achieved through its architecture, because the salivary gland secretion moves into the intestinal system, making it hard for bacteria to overcome this constant flow. We got a first impression of the yet uncharacterized interplay between salivary glands and digestive system, while taking a look at those animals that ectopically express pgrp-le in the salivary glands only. This soluble protein, although produced in the salivary glands only, can migrate through the entire intestinal tract thus functioning as a general activator of the intestinal immune response. It shows that products of the salivary gland have in general the potential to modulate the intestinal immune system, highlighting its importance for intestinal immune homeostasis.
Salivary gland cells, similarly as most epithelial cells, are indeed able to launch an immune response if confronted with an orally applied pathogen. Our experiments demonstrate that two out of three antimicrobial peptide genes are expressed at significantly higher levels; namely, cecropin (cec) and diptericin (dipt). Nevertheless, this increase is not sufficient to be visible in promotor gfp indicator strains. Conventional oral infections are hard to perform and the response characteristics are variable, making it not trivial to identify the major response characteristics of this epithelial immune response. Alternatively, the forced IMD-activation, enables a more focused view on the major characteristics of this type of immune system. Within the salivary gland cells, the response following forced IMD-pathway activation comprises increased expression of antimicrobial peptide genes, which is generally accepted to be the "normal" reaction to this type of stimulus. This clearly shows that the larval salivary gland is an immune competent epithelium, similarly as the intestinal, the airway or the subcuticular epithelium [5–7, 29]. Regarding the set of AMP genes that showed an increased expression, the exceptional role of drosomycin (drs) is suspicious. The lack of Toll-mediated immune signaling appears to be a common feature of all epithelial immune systems characterized in the fly so far [6, 29]. Drosomycin is thought to be the major Toll-pathway dependent antimicrobial peptide; a lack of drosomycin upregulation would thus be in-line with the absence of Toll-mediated signaling in epithelial immunity. Nevertheless, it is puzzling that in the trachea, the only epithelial tissue where a similar experimental approach has been performed, Drosomycin is the major AMP that comes up following infection or ectopic IMD-pathway activation . It has to be mentioned that drosomycin expression is striking in adult salivary glands, which is congruent with earlier findings .
Chronic activation of the salivary gland's immune system comes along with costs for the animal. Reduced sizes in both, the salivary glands and of the entire organism in all its developmental stages, are the result of this activation. The reason for this remains unclear, but apparently, chronic activation impairs the function of the salivary glands, which in turn might result in a reduced capacity to take up nutrients. Therewith, this ectopic regime of epithelial immune system activation shares some commonalities with chronic inflammatory diseases of barrier epithelia . Growth retardation is also seen in children suffering from inflammatory bowel diseases . In these children, malnutrition is obviously not the sole reason for this growth retardation, but the production and regulation of proinflammatory cytokines may also be relevant for this phenotype . Induced expression of membrane tethered proteases such as Presenilin or SPP may thus be a link, as one can speculate that they trigger signaling events while freeing signaling ligands from the membrane. Nevertheless, we have no experimental data if the phenotype inducing processes are restricted to the salivary glands or if they can be attributed to e.g. an increased antimicrobial activity in the intestinal lumen, which in turn may interfere with the microbiota. Although this possibility could not be ruled out, gnotobiotic flies do not show such a significant effect on growth parameters as the one observed in our study.
Surprisingly, only a relatively small group of genes among the cohorts of up- and downregulated ones can be assigned to the set of Drosophila immune genes . Although expression of a complex set of AMP genes is induced, most other induced genes apparently have nothing to do with "conventional" immune responses. This obvious difference between a "conventional" immune response and that of an immune competent epithelium is not restricted to the fly's salivary glands, it can also be seen in another epithelium of the fly, the airways [7, 27]. Apparently, morphological changes that result from chronic immune pathway activation may be one reason for this incongruence. Very surprising is the small overlap between the cohorts of up- or down-regulated genes between the salivary glands and those seen following a natural infection in either the gut or the airways. The same is true for the comparison between IMD-activated transcription in the salivary glands and in the airways, although both experiments were performed with a very similar design. Despite the fact that in both tissues IMD-pathway activation induces an immune response, most parts of the induced response differ substantially between both organs. This indicates that IMD-dependent signaling has only a very small core response shared by all organs and that the tissue specific response is far more important in shaping the transcriptional response following IMD-pathway activation.
A classification according to the gene ontologies revealed some very interesting aspects in both cohorts of genes (up- and downregulated). Among the upregulated genes, both, the ribosome associated as well as the proteasome associated proteins are significantly enriched. Functionally, this would mean that both, the translational capacity and the targeted degradation of proteins intended to proteasomal degradation, are enhanced. KEGG pathway analysis revealed only the oxidative phosphorylation as significantly enriched pathway, which we currently do not understand. Among the cohort of downregulated genes, peptide receptors are conspicuous. A total of six peptide receptors, including all allatostatin receptors  are downregulated. In before, it has not been known that this high number of different neuropeptides have the ability to modulate the activity of salivary glands, which is up to now ascribed to biogenic amines only . Some of the genes that are not part of a conspicuous gene ontology are nevertheless of great interest. Intramembrane proteolysis is thought to be a highly relevant way in cell signaling, which can be fulfilled by only a very small number of proteases. Among them, the presenilin-like proteases are of prime importance. Presenilin proteases gained substantial interest following identification of presenilin mutants being causative for some forms of familial Alzheimer disease . They are part of the gamma-secretase complex, thus having a central role in the formation of amyloid plaques . This concerted activation of the proteases highly relevant for countless signaling systems, may be one major reason for the different transcriptomic responses that can be seen both in the trachea and the salivary gland following identical experimental stimulation protocols. Their role in the immune response of this epithelium is completely enigmatic. Nevertheless, these results offer a unique opportunity to use this natural system to study the physiological significance of them in this extremely simplified model system. The fly's salivary glands are of very simple organization, made of only two cell types. In addition, high amounts of pure material can be generated and the organ is highly amenable to specific genetic interventions of different types including RNAi-mediated gene silencing or specific and timed overexpression.
Two other genes, which are known to be associated with stress or immune responses are also upregulated in this organ, the superoxide dismutase (SOD) and the integrator of stress responses dThor. In the intestinal epithelium, the redox homeostasis appears to be one major way to fight infections while protecting the endogenous microbiota. In this context, reactive oxygen species generated by the dual oxidase Duox are apparently of prime importance. In the salivary gland, only the SOD appears to be upregulated, pointing to a role in defence of the own epithelium in response to a real or to an anticipated infection.
Salivary glands are an integral part of the gastro-intestinal tract. In the fruit fly, they are indispensable for efficient food intake. As they are blind ending tubular organs, they are particularly prone to infections. We were able to show that the fly's salivary glands are able to mount an immune response if they are confronted with pathogens. This response primarily depends on the production of antimicrobial peptides. To study this response in detail, we established an ectopic expression control system that allows activation the epithelial immune system of the salivary glands without pathogen contact. Although they produce antimicrobial peptides, their overall response appears to be specific for the salivary glands. Chronic activation of the salivary gland's immune system is costly, as it induces severe reduction in growth throughout development. This negative effect could be seen in all developmental stages. Surprisingly, a number of different genes are regulated upon ectopic activation of the IMD-pathway. Among them are proteins involved in presenelin function. Studying this molecule, which is central to Alzheimer pathology, may allow us to unravel some of the aspects of presenelin function in a simple but functional environment.
Fly strains and experimental manipulation
For the ectopic expression experiments, we used the Gal4 driver line P [Sgs3-GAL4.PD]TP1, which directs expression into the salivary glands of larvae and adults only. Ectopic activation of the immune system was achieved by crossing these flies to either UAS-pgrp-le or UAS-pgrp-lc comprising flies . UAS-pgrp-le containing flies also carry a drsP::gfp cassette (flies were generously provided by KV Andersen and S Kurata). For control experiments, we generally used the responder line (mainly UAS-pgrp-lc). Flies were raised on standard cornmeal-agar medium at 20°C.
For infection experiments, early 3rd instar larvae were confronted with the gram-negative bacterium Erwinia carotovora according to protocols used in oral infection experiments. Overnight cultures of the bacterium were centrifuged, concentrated (OD600 = 100) and mixed with banana at a ratio of 1:1. Larvae were allowed to feed for 6 h on these bacteria, subsequently, they were allowed to feed for another 6 h on normal medium and the salivary glands were prepared out of the animals and used for further experiments. Using this material, we performed qRT-PCR analyses for drosomycin, cecropin and diptericin (at least using 3 independent experiments).
Manually extraction for the salivary glands of the 3rd larvae instars followed by total RNA extracted using RNAmagic solution from (Bio-Budget technologies GmbH, Krefeld, Germany). cDNA-synthesis was performed using CapFinder as described. Amplification of the cDNA was performed for 26 cycles taking advantage of a long and accurate PCR system. The integrity and quality of the amplificate was checked by gel electrophoresis. This material was used for RT-PCR experiments, qRT-PCR experiments and the production of labeled hybridization probes for DNA-microarray analysis. cDNA used for downstream applications shouldn't have any contamination of the fat bodies and thus was used only, if amplification with oligonucleotides matching the fat body specific gene P6 was not successful. Quantitative RT-PCR was performed with a Lightcycler (Roche Diagnostics, Ingelheim, Germany) using the Takara SYBR Green Real-time PCR kit (Takara Bio Inc, Japan). Probe sets were normalized against the housekeeping gene Rpl 32. At least three independent experiments were performed in duplicate.
Microarray experiments were essentially performed as described before. In brief, equal amounts of amplified and purified cDNA were subjected to T7-based cRNA synthesis. The synthesis was performed with the T7 MEGAscript kit (Ambion, Applera, Darmstadt, Germany) supplemented with aaUTPs (Ambion, Applera, Darmstadt, Germany) for the labeling of the cRNA. Following purification, approximately 10 μg of aminoallyl modified-cRNA was coupled to succinimidyl modified-Cy3 und -Cy5 dyes (GE Healthcare, Freiburg, Germany) in the presence of 50% DMSO and 0.05 M NaHCO3 (pH 9.0) . Coupling reaction was carried out for two hours in the dark followed by purification and precipitation of the labeled cRNA. After assessment of the labeled cRNA approximately 2-3 μg (or 150pmol) of Cy3 and Cy5 labeled probe were used for hybridization. Hybridisation was carried out at 42°C overnight. After hybridization, slides were washed twice with 1 × SSC, 0.1% Triton-X-100 at 60°C for 15 minutes and with 0.1 × SSC, 0.1% Triton-X-100 at 37°C for 15 min. Subsequently, they were washed with 0.1 × SSC for 30 seconds at room temperature and rinsed with water before dried.
Microarray analysis and bioinformatics
Gene expression analysis was performed using the Drosophila OLIGO 14k_version1 gene chip (Canadian Drosophila Microarray Center, University of Toronto, Canada). The slides were scanned with the GenePixTM4000B scanner (Axon Instruments, Molecular Devices, Munich, Germany). For spot finding and generating preliminary result files the raw scanned image files were analyzed using GenePixPro version 6.0 whereas data normalization, quality assurance and control, filtering and clustering were carried out with GeneTraffic (Iobion, Agilent, Waldbronn, Germany) and statistical analysis with the SAM-program package. In search of functional composition of genes significantly affected upon infection and ectopic expression we used the bioinformatics web tool FatiGO.
The DNA-microarray experiments have been deposited in the GEO-database (accession number: GSE20938).
We would like to acknowledge financial support of the Deutsche Forschungsgemeinschaft. This work is an integral part of the SFB Transregio 22 (Teilprojekt A7) and the Cluster of Excellence "Inflammation@interfaces". In addition, we would like to thank Shoichiro Kurata (Tohoku University, Japan), Kathryn V. Anderson (Sloan Kettering Institute, New York, USA) and the Bloomington Drosophila Stock Center (Indiana University, Bloomington, USA) for fly strains. AA received a personal grant of the egyptian government.
- Silverman N, Paquette N: Immunology. The right resident bugs. Science (New York, NY). 2008, 319 (5864): 734-735.View ArticleGoogle Scholar
- Leclerc V, Reichhart JM: The immune response of Drosophila melanogaster. Immunological reviews. 2004, 198: 59-71. 10.1111/j.0105-2896.2004.0130.x.PubMedView ArticleGoogle Scholar
- Lemaitre B, Nicolas E, Michaut L, Reichhart JM, Hoffmann JA: The dorsoventral regulatory gene cassette spatzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell. 1996, 86 (6): 973-983. 10.1016/S0092-8674(00)80172-5.PubMedView ArticleGoogle Scholar
- Lemaitre B, Hoffmann J: The host defense of Drosophila melanogaster. Annual review of immunology. 2007, 25: 697-743. 10.1146/annurev.immunol.25.022106.141615.PubMedView ArticleGoogle Scholar
- Ferrandon D, Jung AC, Criqui M, Lemaitre B, Uttenweiler-Joseph S, Michaut L, Reichhart J, Hoffmann JA: A drosomycin-GFP reporter transgene reveals a local immune response in Drosophila that is not dependent on the Toll pathway. The EMBO journal. 1998, 17 (5): 1217-1227. 10.1093/emboj/17.5.1217.PubMed CentralPubMedView ArticleGoogle Scholar
- Tzou P, Ohresser S, Ferrandon D, Capovilla M, Reichhart JM, Lemaitre B, Hoffmann JA, Imler JL: Tissue-specific inducible expression of antimicrobial peptide genes in Drosophila surface epithelia. Immunity. 2000, 13 (5): 737-748. 10.1016/S1074-7613(00)00072-8.PubMedView ArticleGoogle Scholar
- Wagner C, Isermann K, Fehrenbach H, Roeder T: Molecular architecture of the fruit fly's airway epithelial immune system. BMC genomics. 2008, 9: 446-10.1186/1471-2164-9-446.PubMed CentralPubMedView ArticleGoogle Scholar
- Cronin SJ, Nehme NT, Limmer S, Liegeois S, Pospisilik JA, Schramek D, Leibbrandt A, Simoes Rde M, Gruber S, Puc U: Genome-wide RNAi screen identifies genes involved in intestinal pathogenic bacterial infection. Science (New York, NY). 2009, 325 (5938): 340-343.View ArticleGoogle Scholar
- Buchon N, Broderick NA, Poidevin M, Pradervand S, Lemaitre B: Drosophila intestinal response to bacterial infection: activation of host defense and stem cell proliferation. Cell host & microbe. 2009, 5 (2): 200-211. 10.1016/j.chom.2009.01.003.View ArticleGoogle Scholar
- Ha EM, Oh CT, Bae YS, Lee WJ: A direct role for dual oxidase in Drosophila gut immunity. Science (New York, NY). 2005, 310 (5749): 847-850.View ArticleGoogle Scholar
- Ha EM, Oh CT, Ryu JH, Bae YS, Kang SW, Jang IH, Brey PT, Lee WJ: An antioxidant system required for host protection against gut infection in Drosophila. Developmental cell. 2005, 8 (1): 125-132. 10.1016/j.devcel.2004.11.007.PubMedView ArticleGoogle Scholar
- Liehl P, Blight M, Vodovar N, Boccard F, Lemaitre B: Prevalence of local immune response against oral infection in a Drosophila/Pseudomonas infection model. PLoS pathogens. 2006, 2 (6): e56-10.1371/journal.ppat.0020056.PubMed CentralPubMedView ArticleGoogle Scholar
- Ryu JH, Ha EM, Oh CT, Seol JH, Brey PT, Jin I, Lee DG, Kim J, Lee D, Lee WJ: An essential complementary role of NF-kappaB pathway to microbicidal oxidants in Drosophila gut immunity. The EMBO journal. 2006, 25 (15): 3693-3701. 10.1038/sj.emboj.7601233.PubMed CentralPubMedView ArticleGoogle Scholar
- Vodovar N, Vinals M, Liehl P, Basset A, Degrouard J, Spellman P, Boccard F, Lemaitre B: Drosophila host defense after oral infection by an entomopathogenic Pseudomonas species. Proceedings of the National Academy of Sciences of the United States of America. 2005, 102 (32): 11414-11419. 10.1073/pnas.0502240102.PubMed CentralPubMedView ArticleGoogle Scholar
- Bischoff V, Vignal C, Duvic B, Boneca IG, Hoffmann JA, Royet J: Downregulation of the Drosophila immune response by peptidoglycan-recognition proteins SC1 and SC2. PLoS pathogens. 2006, 2 (2): e14-10.1371/journal.ppat.0020014.PubMed CentralPubMedView ArticleGoogle Scholar
- Zaidman-Remy A, Herve M, Poidevin M, Pili-Floury S, Kim MS, Blanot D, Oh BH, Ueda R, Mengin-Lecreulx D, Lemaitre B: The Drosophila amidase PGRP-LB modulates the immune response to bacterial infection. Immunity. 2006, 24 (4): 463-473. 10.1016/j.immuni.2006.02.012.PubMedView ArticleGoogle Scholar
- Lhocine N, Ribeiro PS, Buchon N, Wepf A, Wilson R, Tenev T, Lemaitre B, Gstaiger M, Meier P, Leulier F: PIMS modulates immune tolerance by negatively regulating Drosophila innate immune signaling. Cell host & microbe. 2008, 4 (2): 147-158. 10.1016/j.chom.2008.07.004.View ArticleGoogle Scholar
- Pal S, Wu L: Guts and glory: balancing microbes and the immune response. Developmental cell. 2005, 8 (1): 1-2.PubMedGoogle Scholar
- Lee WJ: Bacterial-modulated signaling pathways in gut homeostasis. Science signaling. 2008, 1 (21): pe24-10.1126/stke.121pe24.PubMedView ArticleGoogle Scholar
- Andrew DJ: Regulation and formation of the Drosophila salivary glands. Annals of the New York Academy of Sciences. 1998, 842: 55-69. 10.1111/j.1749-6632.1998.tb09632.x.PubMedView ArticleGoogle Scholar
- Andrew DJ, Henderson KD, Seshaiah P: Salivary gland development in Drosophila melanogaster. Mechanisms of development. 2000, 92 (1): 5-17. 10.1016/S0925-4773(99)00321-4.PubMedView ArticleGoogle Scholar
- Isaac DD, Andrew DJ: Tubulogenesis in Drosophila: a requirement for the trachealess gene product. Genes & development. 1996, 10 (1): 103-117. 10.1101/gad.10.1.103.View ArticleGoogle Scholar
- Roeder T, Isermann K, Kabesch M: Drosophila in asthma research. American journal of respiratory and critical care medicine. 2009, 179 (11): 979-983. 10.1164/rccm.200811-1777PP.PubMedView ArticleGoogle Scholar
- Takehana A, Katsuyama T, Yano T, Oshima Y, Takada H, Aigaki T, Kurata S: Overexpression of a pattern-recognition receptor, peptidoglycan-recognition protein-LE, activates imd/relish-mediated antibacterial defense and the prophenoloxidase cascade in Drosophila larvae. Proceedings of the National Academy of Sciences of the United States of America. 2002, 99 (21): 13705-13710. 10.1073/pnas.212301199.PubMed CentralPubMedView ArticleGoogle Scholar
- Al-Shahrour F, Minguez P, Tarraga J, Medina I, Alloza E, Montaner D, Dopazo J: FatiGO +: a functional profiling tool for genomic data. Integration of functional annotation, regulatory motifs and interaction data with microarray experiments. Nucleic acids research. 2007, W91-96. 10.1093/nar/gkm260. 35 Web ServerGoogle Scholar
- De Gregorio E, Spellman PT, Rubin GM, Lemaitre B: Genome-wide analysis of the Drosophila immune response by using oligonucleotide microarrays. Proceedings of the National Academy of Sciences of the United States of America. 2001, 98 (22): 12590-12595. 10.1073/pnas.221458698.PubMed CentralPubMedView ArticleGoogle Scholar
- Wagner C, Isermann K, Roeder T: Infection induces a survival program and local remodeling in the airway epithelium of the fly. Faseb J. 2009, 23 (7): 2045-2054. 10.1096/fj.08-114223.PubMedView ArticleGoogle Scholar
- Lehmann M, Jiang C, Ip YT, Thummel CS: AP-1, but not NF-kappa B, is required for efficient steroid-triggered cell death in Drosophila. Cell death and differentiation. 2002, 9 (5): 581-590. 10.1038/sj.cdd.4401003.PubMedView ArticleGoogle Scholar
- Onfelt Tingvall T, Roos E, Engstrom Y: The imd gene is required for local Cecropin expression in Drosophila barrier epithelia. EMBO reports. 2001, 2 (3): 239-243. 10.1093/embo-reports/kve048.PubMed CentralPubMedView ArticleGoogle Scholar
- Cezard JP, Touati G, Alberti C, Hugot JP, Brinon C, Czernichow P: Growth in paediatric Crohn's disease. Hormone research. 2002, 58 (Suppl 1): 11-15. 10.1159/000064759.PubMedView ArticleGoogle Scholar
- Walters TD, Griffiths AM: Mechanisms of growth impairment in pediatric Crohn's disease. Nat Rev Gastroenterol Hepatol. 2009, 6 (9): 513-523. 10.1038/nrgastro.2009.124.PubMedView ArticleGoogle Scholar
- Kreienkamp HJ, Larusson HJ, Witte I, Roeder T, Birgul N, Honck HH, Harder S, Ellinghausen G, Buck F, Richter D: Functional annotation of two orphan G-protein-coupled receptors, Drostar1 and -2, from Drosophila melanogaster and their ligands by reverse pharmacology. The Journal of biological chemistry. 2002, 277 (42): 39937-39943. 10.1074/jbc.M206931200.PubMedView ArticleGoogle Scholar
- Baumann O, Dames P, Kuhnel D, Walz B: Distribution of serotonergic and dopaminergic nerve fibers in the salivary gland complex of the cockroach Periplaneta americana. BMC physiology. 2002, 2: 9-10.1186/1472-6793-2-9.PubMed CentralPubMedView ArticleGoogle Scholar
- Link CD: Invertebrate models of Alzheimer's disease. Genes, brain, and behavior. 2005, 4 (3): 147-156. 10.1111/j.1601-183X.2004.00105.x.PubMedView ArticleGoogle Scholar
- Takasugi N, Tomita T, Hayashi I, Tsuruoka M, Niimura M, Takahashi Y, Thinakaran G, Iwatsubo T: The role of presenilin cofactors in the gamma-secretase complex. Nature. 2003, 422 (6930): 438-441. 10.1038/nature01506.PubMedView ArticleGoogle Scholar
- Franz O, Bruchhaus I, Roeder T: Verification of differential gene transcription using virtual northern blotting. Nucleic acids research. 1999, 27 (11): e3-10.1093/nar/27.11.e3.PubMed CentralPubMedView ArticleGoogle Scholar
- t'Hoen PA, de Kort F, van Ommen GJ, den Dunnen JT: Fluorescent labelling of cRNA for microarray applications. Nucleic acids research. 2003, 31 (5): e20-10.1093/nar/gng020.View ArticleGoogle 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.