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A CONSERVED SIGNALING PATHWAY: The Drosophila Toll-Dorsal Pathway
Abstract
▪ Abstract The Toll-Dorsal pathway in Drosophila and the interleukin-1 receptor (IL-1R)-NF-κB pathway in mammals are homologous signal transduction pathways that mediate several different biological responses. In Drosophila, genetic analysis of dorsal-ventral patterning of the embryo has defined the series of genes that mediate the Toll-Dorsal pathway. Binding of extracellular ligand activates the transmembrane receptor Toll, which requires the novel protein Tube to activate the cytoplasmic serine/threonine kinase Pelle. Pelle activity controls the degradation of the Cactus protein, which is present in a cytoplasmic complex with the Dorsal protein. Once Cactus is degraded in response to signal, Dorsal is free to move into the nucleus where it regulates transcription of specific target genes. The Toll, tube, pelle, cactus, and dorsal genes also appear to be involved in Drosophila immune response. Because the IL-1R-NF-κB pathway plays a role in vertebrate innate immunity and because plant homologues of the Toll-Dorsal pathway are important in plant disease resistance, it is likely that this pathway arose before the divergence of plants and animals as a defense against pathogens.
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“With the exception of Weckle, this intracellular signaling module is well conserved in vertebrates in which the homologs are involved in regulation of the immune response”
From Graded dorsal and differential gene regulation in the Drosophila embryo. (2009) · cites this paper as Belvin and Anderson 1996
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Research works printed but not linked: 106
- 10.1128/MCB.15.3.1294 · DOI
- 10.1016/0092-8674(85)90274-0 · DOI · Paper page
- 10.1038/311223a0 · DOI
- Anderson KV, Nüsslein-Volhard C. 1986. Dorsal-group genes of Drosophila. InGametogenesis and the Early Embryo, ed. J Gall, pp. 177–94. New York: Liss
- Åsling B, 1995, 36th Annu. Drosophila Res. Conf.
- 10.1016/0092-8674(88)90382-0 · DOI
- 10.1128/MCB.13.6.3301 · DOI
- 10.1101/gad.9.22.2736 · DOI
- 10.1038/376167a0 · DOI
- 10.1101/gad.9.7.783 · DOI · Paper page
- Betts JC, 1993, J. Biol. Chem., 268, 25624, 10.1016/S0021-9258(19)74435-4 · DOI
- 10.1126/science.7878466 · DOI · Paper page
- 10.1126/science.271.5252.1128 · DOI
- 10.1101/gad.9.13.1586 · DOI
- Ciechanover A, 1994, Biol. Chem. Hoppe-Seyler, 375, 565
- 10.1042/bj3000567 · DOI
- 10.1074/jbc.270.28.16514 · DOI
- 10.1128/MCB.15.3.1302 · DOI · Paper page
- 10.1006/jmbi.1993.1392 · DOI
- Fey GH, Gauldie J. 1990. InProgress in Liver Disease, ed. H Topper, F Schaffner, pp. 89–116. Philadelphia: Saunders
- Galindo RL, 1995, Development, 121, 2209, 10.1242/dev.121.7.2209 · DOI
- 10.1091/mbc.3.12.1339 · DOI
- 10.1016/0092-8674(92)90595-4 · DOI
- Gerttula S, 1988, Genetics, 119, 123, 10.1093/genetics/119.1.123 · DOI
- 10.1128/MCB.14.6.3559 · DOI
- 10.1016/B978-0-08-030804-3.50017-0 · DOI
- 10.1128/MCB.16.3.1103 · DOI
- 10.1038/372563a0 · DOI
- 10.1006/dbio.1995.1134 · DOI
- Hashimoto C, 1991, Development, 111, 1021, 10.1242/dev.111.4.1021 · DOI
- 10.1016/0092-8674(88)90516-8 · DOI
- 10.1016/0092-8674(91)90022-Q · DOI
- 10.1002/j.1460-2075.1993.tb05939.x · DOI
- Hecht PM, 1993, Genetics, 135, 405, 10.1093/genetics/135.2.405 · DOI · Paper page
- Heguy A, 1992, J. Biol. Chem., 267, 2605, 10.1016/S0021-9258(18)45924-8 · DOI
- 10.1038/365182a0 · DOI
- 10.1016/0092-8674(92)90083-O · DOI
- 10.1016/0952-7915(95)80022-0 · DOI
- 10.1016/0168-9525(93)90165-E · DOI
- 10.1016/0092-8674(91)90651-E · DOI
- 10.1016/0959-437X(94)90133-N · DOI
- 10.1101/gad.6.9.1728 · DOI
- 10.1101/gad.6.8.1518 · DOI
- 10.1016/0092-8674(93)90495-C · DOI
- 10.1073/pnas.91.12.5350 · DOI
- 10.1101/gad.6.4.619 · DOI
- 10.1128/MCB.15.4.2166 · DOI
- 10.1016/0092-8674(93)90402-C · DOI
- 10.1002/j.1460-2075.1992.tb05387.x · DOI · Paper page
- 10.1126/science.7973631 · DOI
- 10.1002/j.1460-2075.1993.tb05800.x · DOI
- 10.1002/j.1460-2075.1990.tb07878.x · DOI
- 10.1016/0092-8674(92)90596-5 · DOI
- Koj A. 1985. Liver response to inflammation and synthesis of acute-phase plasma proteins. InThe Acute-Phase Response to Injury and Infection. Research Monographs in Cell and Tissue Physiology, ed. AH Gordon, A Koj, pp. 139–246. Amsterdam: Elsevier
- 10.1016/S0065-2776(08)60618-5 · DOI
- 10.1073/pnas.89.17.8145 · DOI
- 10.1073/pnas.92.22.10242 · DOI
- 10.1038/371175a0 · DOI
- 10.1002/j.1460-2075.1995.tb07029.x · DOI
- 10.1073/pnas.88.3.810 · DOI
- 10.1002/j.1460-2075.1993.tb06019.x · DOI
- 10.1073/pnas.92.2.552 · DOI
- 10.1016/0012-1606(79)90065-4 · DOI
- 10.1126/science.7902614 · DOI
- 10.1105/tpc.6.11.1543 · DOI
- 10.1002/eji.1830240717 · DOI
- 10.1073/pnas.90.21.10193 · DOI · Paper page
- 10.1073/pnas.91.26.12740 · DOI
- 10.1016/S0065-230X(08)60257-2 · DOI
- 10.1016/0092-8674(94)90507-X · DOI
- 10.1146/annurev.genet.29.1.371 · DOI
- 10.1016/0014-5793(95)00541-G · DOI
- 10.1101/gad.6.9.1654 · DOI
- 10.1016/0092-8674(92)90426-D · DOI
- 10.1101/gad.5.10.1892 · DOI
- 10.1016/0968-0004(94)90115-5 · DOI
- 10.1002/j.1460-2075.1995.tb07317.x · DOI
- Rechsteiner M, 1990, Semin. Cell Biol., 1, 433
- Reichhart JM, 1993, CR Acad. Sci. III, 316, 1218
- 10.1002/j.1460-2075.1992.tb05191.x · DOI
- 10.1128/MCB.15.5.2413 · DOI
- 10.1126/science.2876518 · DOI
- Roth S, 1991, Development, 112, 371, 10.1242/dev.112.2.371 · DOI
- 10.1016/0092-8674(89)90774-5 · DOI
- 10.1016/0092-8674(89)90772-1 · DOI
- 10.1073/pnas.90.19.8842 · DOI
- 10.1073/pnas.92.24.11259 · DOI
- 10.1101/gad.5.5.797 · DOI · Paper page
- Schneider DS, 1994, Development, 120, 1243, 10.1242/dev.120.5.1243 · DOI
- 10.1128/MCB.15.7.3960 · DOI
- 10.1016/0092-8674(95)90415-8 · DOI
- 10.1016/0092-8674(93)90071-W · DOI
- 10.1146/annurev.cb.10.110194.002201 · DOI
- Sipe JD. 1985. Cellular and humoral components of the early inflammatory reaction. InThe Acute-Phase Response to Injury and Infection. Research Monographs in Cell and Tissue Physiology, ed. AH Gordon, A Koj, pp. 3–21. Amsterdam: Elsevier
- 10.1126/science.270.5243.1804 · DOI
- 10.1126/science.7732374 · DOI
- 10.1126/science.3118464 · DOI
- 10.1016/0092-8674(89)90773-3 · DOI
- Sun SC, 1991, J. Biol. Chem., 266, 6644, 10.1016/S0021-9258(18)38165-1 · DOI
- 10.1128/MCB.15.7.3627 · DOI
- 10.1016/0092-8674(91)90014-P · DOI
- 10.1002/j.1460-2075.1994.tb06878.x · DOI
- 10.1016/0092-8674(95)90416-6 · DOI
- 10.1083/jcb.123.3.523 · DOI
- 10.1016/0092-8674(94)90283-6 · DOI
- 10.1016/0092-8674(95)90208-2 · DOI
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Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394
A human homologue of the Drosophila Toll protein signals activation of adaptive immunity
Medzhitov, R., Preston-Hurlburt, P., & Janeway, C. A. J. (1997) · Nature · doi:10.1038/41131 · Cited by 6,137
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Takeuchi, O., Hoshino, K., Kawai, T., Sanjo, H., Takada, H., Ogawa, T., Takeda, K., & Akira, S. (1999) · Immunity · doi:10.1016/s1074-7613(00)80119-3 · Cited by 3,680
The host defense of Drosophila melanogaster.
Lemaître, B., & Hoffmann, J. (2007) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141615 · Cited by 3,404
“The Toll pathway is an evolutionarily conserved signaling cascade that plays a key role in the establishment of the dorso-ventral axis of the Drosophila embryo, as well as in several other developmental processes (42).”
BackgroundHoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Takeda, K., & Akira, S. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.3749 · Cited by 3,374
Takeda, K., Kaisho, T., & Akira, S. (2003) · Annual Review of Immunology · doi:10.1016/b0-12-443710-9/00729-8 · Cited by 2,947
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LPS induction of gene expression in human monocytes
Guha, M., & Mackman, N. (2001) · Cellular Signalling · doi:10.1016/s0898-6568(00)00149-2 · Cited by 2,333
Unresponsiveness of MyD88-deficient mice to endotoxin.
Kawai, T., Adachi, O., Ogawa, T., Takeda, K., & Akira, S. (1999) · Immunity · doi:10.1016/s1074-7613(00)80086-2 · Cited by 2,367
Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function.
Adachi, O., Kawai, T., Takeda, K., Matsumoto, M., Tsutsui, H., Sakagami, M., Nakanishi, K., & Akira, S. (1998) · Immunity · doi:10.1016/s1074-7613(00)80596-8 · Cited by 2,358
A family of human receptors structurally related to Drosophila Toll.
Rock, F., Hardiman, G., Timans, J., Kastelein, R., & Bazan, J. (1998) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.95.2.588 · Cited by 2,009
Toll-like Receptor-4 Mediates Lipopolysaccharide-induced Signal Transduction
Chow, J. C., Young, D. W., Golenbock, D. T., Christ, W. J., & Gusovsky, F. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.16.10689 · Cited by 1,924
Pattern recognition receptors TLR4 and CD14 mediate response to respiratory syncytial virus
Kurt-Jones, E., Popova, L., Kwinn, L. A., Haynes, L., Jones, L. P., Tripp, R., Walsh, E., Freeman, M., Golenbock, D., Anderson, L., et al. (2000) · Nature Immunology · doi:10.1038/80833 · Cited by 1,842
MyD88 is an adaptor protein in the hToll/IL-1 receptor family signaling pathways.
Medzhitov, R., Preston-Hurlburt, P., Kopp, E., Stadlen, A., Chen, C.-Q., Ghosh, S., & Janeway, C. (1998) · Molecules and Cells · doi:10.1016/s1097-2765(00)80136-7 · Cited by 1,783
Comparative Genomics of the Eukaryotes
Rubin, G. M., Yandell, M. D., Wortman, J. R., Gabor, G. L., Miklos, Nelson, C. R., Hariharan, I. K., Fortini, M. E., Li, P. W., Apweiler, R., et al. (2000) · Science · doi:10.1126/science.287.5461.2204 · Cited by 1,698
Innate immune recognition: mechanisms and pathways
Medzhitov, R., & Janeway, C. (2000) · Immunological Reviews · doi:10.1034/j.1600-065x.2000.917309.x · Cited by 1,589
“components of this pathway were identified through genetic analyses (31).”
BackgroundThe immune response of Drosophila
Hoffmann, J. A. (2003) · Nature · doi:10.1038/nature02021 · Cited by 1,553
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BackgroundToll-like receptor-2 mediates lipopolysaccharide-induced cellular signalling
Yang, R.-B., Mark, M., Gray, A., Huang, A., Xie, M.-H., Zhang, M., Goddard, A., Wood, W., Gurney, A., & Godowski, P. (1998) · Nature · doi:10.1038/26239 · Cited by 1,319
“In Drosophila , the Toll receptor participates in establishing the dorsoventral pattern in the embryo and inducing an antifungal immune response in the adult fl”
BackgroundMyD88: an adapter that recruits IRAK to the IL-1 receptor complex.
Wesche, H., Henzel, W., Shillinglaw, W., Li, S., & Cao, Z.-D. (1997) · Immunity · doi:10.1016/s1074-7613(00)80402-1 · Cited by 1,247
Drosophila innate immunity: an evolutionary perspective
Hoffmann, J. A., & Reichhart, J. (2002) · Nature Immunology · doi:10.1038/ni0202-121 · Cited by 1,168
Flynn, J., & Chan, J. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.93 · Cited by 1,144
Helical Assembly in the MyD88-IRAK4-IRAK2 Complex in TLR/IL-1R Signalling
Lin, S.-C., Lo, Y.-C., & Wu, H. (2010) · Nature · doi:10.1038/nature09121 · Cited by 1,111
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Lien, E., Sellati, T., Yoshimura, A., Flo, T., Rawadi, G., Finberg, R., Carroll, J. D., Espevik, T., Ingalls, R., Radolf, J., et al. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.47.33419 · Cited by 1,062
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Ausubel, F. M. (2005) · Nature Immunology · doi:10.1038/ni1253 · Cited by 1,013
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Karin, M. (1999) · Oncogene · doi:10.1038/sj.onc.1203219 · Cited by 1,160
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Valanne, S., Wang, J., & Rämet, M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002302 · Cited by 888
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BackgroundFeldman, R. M. R., Correll, C. C., Kaplan, K. B., & Deshaies, R. J. (1997) · Cell · doi:10.1016/s0092-8674(00)80404-3 · Cited by 820
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BackgroundTlr4: central component of the sole mammalian LPS sensor.
Beutler, B. (2000) · Current Opinion in Immunology · doi:10.1016/s0952-7915(99)00046-1 · Cited by 847
Zhang, G., & Ghosh, S. (2001) · Journal of Clinical Investigation · doi:10.1172/jci11837 · Cited by 781
“Interestingly, TLR-mediated NF-κB activation is also an evolutionarily conserved event that occurs in phylogenetically distinct species ranging from insects to mammals (5, 9, 10).”
BackgroundResultInfluentialMichel, T., Reichhart, J., Hoffmann, J. A., & Royet, J. (2001) · Nature · doi:10.1038/414756a · Cited by 818
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BackgroundToll-like receptor 4 imparts ligand-specific recognition of bacterial lipopolysaccharide.
Lien, E., Means, T., Heine, H., Yoshimura, A., Kusumoto, S., Fukase, K., Fenton, M., Oikawa, M., Qureshi, N., Monks, B., et al. (2000) · Journal of Clinical Investigation · doi:10.1172/jci8541 · Cited by 798
Gene regulatory networks for development
Levine, M., & Davidson, E. H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408031102 · Cited by 796
Plant Receptor-Like Kinase Gene Family: Diversity, Function, and Signaling
Shiu, S., & Bleecker, A. (2001) · Science's STKE · doi:10.1126/stke.2001.113.re22 · Cited by 759
“Pelle is involved in determining both dorsal and ventral patterning and innate immunity in fly (42).”
BackgroundHuman toll-like receptor 2 confers responsiveness to bacterial lipopolysaccharide
Kirschning, C. J., Wesche, H., Merrill Ayres, T., & Rothe, M. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.11.2091 · Cited by 753
“The observation that human TLR4 (hToll) may function in the innate immune system in vertebrates similar to Toll in Drosophila (6) prompted us to investigate if members of the mammalian TLR family might participate in the recognition of bacterial LPS.”
BackgroundResultInfluentialThe Toll receptor family and microbial recognition
Medzhitov, R. M., & Janeway, C. A. (2000) · Trends in Microbiology · doi:10.1016/s0966-842x(00)01845-x · Cited by 683
The Toll-receptor family and control of innate immunity.
Kopp, E., & Medzhitov, R. (1999) · Current Opinion in Immunology · doi:10.1016/s0952-7915(99)80003-x · Cited by 734
Toll-like receptors and innate immunity
Kumar, H., Kawai, T., & Akira, S. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.08.062 · Cited by 1,221
Zhang, F. X., Kirschning, C., Mancinelli, R., Xu, X.-P., Jin, Y., Faure, E., Mantovani, A., Rothe, M., Muzio, M., & Arditi, M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.12.7611 · Cited by 702
Structure and Function of Toll Receptors and Their Ligands
Gay, N. J., & Gangloff, M. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060305.151318 · Cited by 690
The evolution and genetics of innate immunity
Kimbrell, D., & Beutler, B. (2001) · Nature reviews genetics · doi:10.1038/35066006 · Cited by 679
Toll signaling pathways in the innate immune response
Anderson, K. V. (2000) · Current Opinion in Immunology · doi:10.1016/s0952-7915(99)00045-x · Cited by 634
Self-citationInnate Immunity toMycobacterium tuberculosis
van Crevel, R., Ottenhoff, T. H. M., & van der Meer, J. W. M. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.2.294-309.2002 · Cited by 602
“recognition on macrophages and dendritic cells (20, 135, 240).”
BackgroundThe interleukin‐1 receptor/Toll‐like receptor superfamily: 10 years of progress
O'Neill, L. A. J. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00701.x · Cited by 623
Faure, E., Equils, O., Sieling, P., Thomas, L., Zhang, F. X., Kirschning, C., Polentarutti, N., Muzio, M., & Arditi, M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.15.11058 · Cited by 606
Positive Correlation between Virulence ofPseudomonas aeruginosa Mutants in Mice and Insects
Jander, G., Rahme, L., & Ausubel, F. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.13.3843-3845.2000 · Cited by 594
“Since specific Drosophila mutants with increased sensitivity to microbial infections are known (1, 13), combining such insect mutants with avirulent PA14 mutants might help to elucidate the process of infection, perhaps showing which host defensive systems are needed to counteract specific bacterial virulence factors.”
BackgroundToll-like receptors — taking an evolutionary approach
Leulier, F., & Lemaitre, B. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2303 · Cited by 581
“The intracellular domain of TLRs has been associated with the signalling cascade leading to the nuclear translocation of the transcription factor NF-κ”
TLR2 is expressed on activated T cells as a costimulatory receptor
Komai‐Koma, M., Jones, L., Ogg, G. S., Xu, D., & Liew, F. Y. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400171101 · Cited by 487
The NF-κB Activation Pathway: A Paradigm in Information Transfer from Membrane to Nucleus
Rothwarf, D., & Karin, M. (1999) · Science's STKE · doi:10.1126/stke.1999.5.re1 · Cited by 553
Expression analysis of the Toll-like receptor and TIR domain adaptor families of zebrafish.
Meijer, A. H., Krens, S. F. G., Medina-Rodríguez, I., He, S.-N., Bitter, W., Snaar-Jagalska, B., & Spaink, H. (2004) · Molecular Immunology · doi:10.1016/j.molimm.2003.10.003 · Cited by 553
Toll-like receptors; their physiological role and signal transduction system
Takeuchi, O., & Akira, S. (2001) · International Immunopharmacology · doi:10.1016/s1567-5769(01)00010-8 · Cited by 464
Barnes, P. J. (1997) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(96)00159-8 · Cited by 498
Murine retroviruses activate B cells via interaction with toll-like receptor 4
Rassa, J., Meyers, J., Zhang, Y., Kudaravalli, R., & Ross, S. (2002) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.042355399 · Cited by 493
The proPO and clotting system in crustaceans
Sritunyalucksana, K., & Söderhäll, K. (2000) · Aquaculture · doi:10.1016/s0044-8486(00)00411-7 · Cited by 480
IRAK-M Is a Novel Member of the Pelle/Interleukin-1 Receptor-associated Kinase (IRAK) Family*
Wesche, H., Gao, X., Li, X.-X., Kirschning, C., Stark, G., & Cao, Z.-D. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.27.19403 · Cited by 475
Toll receptors in innate immunity.
Imler, J., & Hoffmann, J. (2001) · Trends in Cell Biology · doi:10.1016/s0962-8924(01)02004-9 · Cited by 474
Binding of the Drosophila cytokine Spätzle to Toll is direct and establishes signaling
Weber, A. N. R., Tauszig-Delamasure, S., Hoffmann, J. A., Lelièvre, E., Gascan, H., Ray, K. P., Morse, M. A., Imler, J.-L., & Gay, N. J. (2003) · Nature Immunology · doi:10.1038/ni955 · Cited by 469
“, in addition to its long-known function in embryonic dorso-ventral patternin”
BackgroundConstitutive activation of toll-mediated antifungal defense in serpin-deficient Drosophila.
Levashina, E., Langley, E., Green, C., Gubb, D., Ashburner, M., Hoffmann, J. A., & Reichhart, J. (1999) · Science · doi:10.1126/science.285.5435.1917 · Cited by 469
Toll-like receptors in neurodegeneration
Okun, E., Griffioen, K. J. S., Lathia, J. D., Tang, S., Mattson, M. P., & Arumugam, T. V. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.09.001 · Cited by 444
A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans
Pujol, N., Link, E. M., Liu, L. X., Kurz, C. L., Alloing, G., Tan, M., Ray, K. P., Solari, R. C. E., Johnson, C. D., & Ewbank, J. J. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00241-x · Cited by 450
Faure, E., Thomas, L. S., Xu, H., Medvedev, A. E., Equils, O., & Arditi, M. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.3.2018 · Cited by 443
Groucho/TLE family proteins and transcriptional repression.
Chen, G.-Q., & Courey, A. (2000) · Gene · doi:10.1016/s0378-1119(00)00161-x · Cited by 437
Pastorelli, L., Salvo, C. D., Mercado, J. R., Vecchi, M. L., & Pizarro, T. T. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00280 · Cited by 446
Toll-related receptors and the control of antimicrobial peptide expression in Drosophila.
Tauszig, S., Jouanguy, E., Hoffmann, J. A., & Imler, J. (2000) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.180130797 · Cited by 429
Stress-hyperglycemia, insulin and immunomodulation in sepsis
Marik, P. E., & Raghavan, M. (2004) · Intensive Care Medicine · doi:10.1007/s00134-004-2167-y · Cited by 423
“In addition, cytokines such as TNF-a and IL-1 and catecholamines independently and synergistically promote hepatic glucose production [38, 39].”
BackgroundInfluentialSerine proteinase inhibitors in arthropod immunity.
Kanost, M. (1999) · Developmental and Comparative Immunology · doi:10.1016/s0145-305x(99)00012-9 · Cited by 427
Recent advances in researches on the innate immunity of shrimp in China
Li, F., & Xiang, J. (2012) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2012.03.016 · Cited by 455
A universal role for MyD88 in TLR/IL-1R-mediated signaling
Janssens, S., & Beyaert, R. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)02145-x · Cited by 417
Tzou, P., Gregorio, E. D., & Lemaître, B. (2002) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(02)00294-1 · Cited by 399
ENDOSPERM DEVELOPMENT: Cellularization and Cell Fate Specification.
Olsen, O. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.233 · Cited by 386
The clip-domain family of serine proteinases in arthropods.
Jiang, H.-B., & Kanost, M. (2000) · Insect Biochemistry and Molecular Biology · doi:10.1016/s0965-1748(99)00113-7 · Cited by 380
Signaling pathways regulating innate immune responses in shrimp.
Li, F.-H., & Xiang, J. (2013) · Fish and Shellfish Immunology · doi:10.1016/j.fsi.2012.08.023 · Cited by 377
The immunobiology of the TLR9 subfamily.
Wagner, H. (2004) · Trends in immunology · doi:10.1016/j.it.2004.04.011 · Cited by 375
Drosophila: the genetics of innate immune recognition and response.
Brennan, C., & Anderson, K. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104626 · Cited by 370
Self-citationA pol I transcriptional body associated with VSG mono-allelic expression in Trypanosoma brucei
Navarro, M., & Gull, K. (2001) · Nature · doi:10.1038/414759a · Cited by 362
Innate immunity and the normal microflora
Boman, H. G. (2000) · Immunological Reviews · doi:10.1034/j.1600-065x.2000.917301.x · Cited by 360
“They were first found in Drosophila development (10), then in human cell lines (11, 12), but soon”
BackgroundA Drosophila IkappaB kinase complex required for Relish cleavage and antibacterial immunity.Preprint
Silverman, N., Zhou, R., Stöven, S., Pandey, N. B., Hultmark, D., & Maniatis, T. (2000) · Genes & Development · doi:10.1101/gad.817800 · Cited by 347
“Dorsal, but not Dif, is required for the dorsoventral pathway (Belvin and Anderson 1996).”
BackgroundVidal, S., Khush, R. S., Leulier, F., Tzou, P., Nakamura, M., & Lemaitre, B. (2001) · Genes & Development · doi:10.1101/gad.203301 · Cited by 311
“…analysis combining a Toll gain-of-function mutation that constitutively activates the Toll pathway and lossof-function mutations in other genes was a powerful tool for establishing the order of action of the genes encoding components of the Toll pathway (for review, see Belvin and Anderson 1996).”
MethodInflammatory signals regulate hematopoietic stem cells
Baldridge, M. T., King, K. Y., & Goodell, M. A. (2011) · Trends in Immunology · doi:10.1016/j.it.2010.12.003 · Cited by 351
ECSIT is an evolutionarily conserved intermediate in the Toll/IL-1 signal transduction pathway
Kopp, E., Medzhitov, R., Carothers, J., Xiao, C., Douglas, I., Janeway, C. A., & Ghosh, S. (1999) · Genes & Development · doi:10.1101/gad.13.16.2059 · Cited by 334
Matsuguchi, T., Takagi, A., Matsuzaki, T., Nagaoka, M., Ishikawa, K., Yokokura, T., & Yoshikai, Y. (2003) · Clinical Diagnostic Laboratory Immunology · doi:10.1128/cdli.10.2.259-266.2003 · Cited by 328
“Toll, first identified as a protein controlling dorsoventral pattern formation in the early development of Drosophila melanogaster (2), has been shown to participate in antimicrobial immune responses (16).”
BackgroundAn ancient system of host defense
Medzhitov, R., & Janeway, C. A. (1998) · Current Opinion in Immunology · doi:10.1016/s0952-7915(98)80024-1 · Cited by 327
Human lung cancer cells express functionally active Toll-like receptor 9
Droemann, D., Albrecht, D., Gerdes, J., Ulmer, A., Branscheid, D., Vollmer, E., Dalhoff, K., Zabel, P., & Goldmann, T. (2005) · Respiratory Research · doi:10.1186/1465-9921-6-1 · Cited by 327
Regulated nuclear import of Rel proteins in the Drosophila immune response
Wu, L. P., & Anderson, K. (1998) · Nature · doi:10.1038/32195 · Cited by 324
“The Toll signalling pathway, which controls dorsal–ventral patterning during Drosophila embryogenesi”
BackgroundSelf-citationMatsuguchi, T., Musikacharoen, T., Ogawa, T., & Yoshikai, Y. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.10.5767 · Cited by 279
Whole-genome analysis of dorsal-ventral patterning in the Drosophila embryo.
Stathopoulos, A., Drenth, M. V., Erives, A. J., Markstein, M., & Levine, M. (2002) · Cell · doi:10.1016/s0092-8674(02)01087-5 · Cited by 310
“It is ini-Division of Genetics and Development 401 Barker Hall tially distributed throughout the cytoplasm of develop- ing oocytes but is transported into nuclei shortly afterUniversity of California, Berkeley Berkeley, California 94720 fertilization (reviewed by Belvin and Anderson, 1996).”
BackgroundZhang, G., & Ghosh, S. (2000) · Journal of Endotoxin Research · doi:10.1179/096805100101532414 · Cited by 316
Type II transmembrane serine proteases.
Wu, Q. (2003) · Current Topics in Developmental Biology · doi:10.1016/s0070-2153(03)54009-1 · Cited by 299
The 18‐wheeler mutation reveals complex antibacterial gene regulation in Drosophila host defense
Williams, M. J., Rodriguez, A., Kimbrell, D., & Eldon, E. D. (1997) · EMBO Journal · doi:10.1093/emboj/16.20.6120 · Cited by 297
“…of a variety of organisms as well as in Drosophila development has been discussed extensively (see for example Hultmark, 1993; Wasserman, 1993; Belvin and Anderson, 1996) and testifies to the efficiency of the IL1R–Rel pathway in effecting rapid and specific changes in transcriptional…”
BackgroundHost defence peptides from invertebrates--emerging antimicrobial strategies.
Hancock, R., Brown, K. L., & Mookherjee, N. (2006) · Immunobiology · doi:10.1016/j.imbio.2005.10.017 · Cited by 290
“…transduction pathway resulting in phosphorylation of an IkB-like inhibitor Cactus causing it to dissociate from the NFkB-like transcription factor DIF, which in turn translocates to the nucleus and activates numerous antimicrobial genes (Belvin and Anderson, 1996; Hoffmann and Reichhart, 2002).”
BackgroundPatterns of Gene Expression During Drosophila Mesoderm Development
Furlong, E., Andersen, E. C., Null, B. H., White, K., & Scott, M. (2001) · Science · doi:10.1126/science.1062660 · Cited by 286
Ma, Y., Li, J., Chiu, I., Wang, Y., Sloane, J. A., Lü, J., Kosaras, B., Sidman, R. L., Volpe, J. J., & Vartanian, T. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200606016 · Cited by 237
“In addition to a well-described role in immunity (Hoffmann, 2003), Toll, which is the Drosophila melanogaster orthologue of the TLRs, plays crucial roles in establishing the dorsoventral axis polarity during embryogenesis (Belvin and Anderson, 1996), in synaptogenesis, and in axon pathfi nding (Rose et al.”
Heine, H., Kirschning, C. J., Lien, E., Monks, B. G., Rothe, M., & Golenbock, D. T. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.12.6971 · Cited by 230
Su, G. L., Klein, R., Aminlari, A., Zhang, H. Y., Steinstraesser, L., Alarcon, W. H., Remick, D., & Wang, S. C. (2000) · Hepatology · doi:10.1053/he.2000.5634 · Cited by 280
Wang, P., & Ohura, K. (2002) · Critical Reviews in Oral Biology and Medicine · doi:10.1177/154411130201300204 · Cited by 278
Iwami, K.-I., Matsuguchi, T., Masuda, A., Kikuchi, T., Musikacharoen, T., & Yoshikai, Y. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.12.6682 · Cited by 273
Jiang, H.-B., Wang, Y., & Kanost, M. (1998) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.95.21.12220 · Cited by 273
Metadata
- Authors
- Belvin, M. P., & Anderson, K. V.
- Affiliations
- University of California, Berkeley (US)
- Venue
- Annual Review of Cell and Developmental Biology
- Publisher
- Annual Reviews
- Published
- 1996-11
- Volume
- 12
- Issue
- 1
- Pages
- 393-416
- ISSN
- 1081-0706 (ISSN-L)
- 1530-8995
- OpenAlex
- W2098336582
- Cited by
- 836
- References
- 0
- Citations by year
- 2026: 7 · 2025: 14 · 2024: 24 · 2023: 18 · 2022: 23 · 2021: 22 · 2020: 12 · 2019: 21 · 2018: 23 · 2017: 17 · 2016: 17 · 2015: 24 · 2014: 24 · 2013: 25 · 2012: 19
- FWCI
- 5.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Cell and Developmental Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Immunology and Microbiology › Immunology › Invertebrate Immune Response Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- Drosophila, Toll receptor, tubes, dorsoventral patterning, embryonic patterning, innate immunity, interleukin-1 receptor, NF-κB, evolution of signaling pathways, plant disease resistance, conserved signaling pathways
- MeSH terms
- Animals, Drosophila, Signal Transduction, Gene Expression Regulation, Developmental
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