SEARCH

SEARCH BY CITATION

References

  • 1
    Bosch, X., Lozano, F., Cervera, R., Ramos-Casals, M.andMin, B., Basophils, IgE, and autoantibody-mediated kidney disease. J. Immunol. 2011. 186: 60836090.
  • 2
    Schroeder, J. T., Basophils: emerging roles in the pathogenesis of allergic disease. Immunol. Rev. 2011. 242: 144160.
  • 3
    Schwartz, C. and Voehringer, D., Basophils: important emerging players in allergic and anti-parasite responses. BioEssays 2011. 33: 423426.
  • 4
    Voehringer, D., Basophils in allergic immune responses. Curr. Op. Immunol.2011. 23: 789793.
  • 5
    Voehringer, D., Basophils in immune responses against helminths. Microbes Infect. 2011. 13: 881887.
  • 6
    Zdanov, A., Structural analysis of cytokines comprising the IL-10 family. Cytokine Growth Factor Rev. 2010. 21: 325330.
  • 7
    Leonard, W. J., Cytokines and immunodeficiency diseases. Nat. Rev. Immunol. 2001. 1: 200208.
  • 8
    Novatchkova, M., Leibbrandt, A., Werzowa, J., Neubuser, A. and Eisenhaber, F., The STIR-domain superfamily in signal transduction, development and immunity. Trends Biochem. Sci. 2003. 28: 226229.
  • 9
    Ohnmacht, C. and Voehringer, D., Basophil effector function and homeostasis during helminth infection. Blood 2009. 113: 28162825.
  • 10
    Iwasaki, H., Mizuno, S., Arinobu, Y., Ozawa, H., Mori, Y., Shigematsu, H., Takatsu, K. et al., The order of expression of transcription factors directs hierarchical specification of hematopoietic lineages. Genes Dev. 2006. 20: 30103021.
  • 11
    Arinobu, Y., Iwasaki, H., Gurish, M. F., Mizuno, S., Shigematsu, H., Ozawa, H., Tenen, D. G. et al., Developmental checkpoints of the basophil/mast cell lineages in adult murine hematopoiesis. Proc. Natl. Acad. Sci. USA 2005. 102: 1810518110.
  • 12
    Siracusa, M. C., Saenz, S. A., Hill, D. A., Kim, B. S., Headley, M. B., Doering, T. A., Wherry, E. J. et al., TSLP promotes interleukin-3-independent basophil haematopoiesis and type 2 inflammation. Nature 2011. 477: 229233.
  • 13
    Ohmori, K., Luo, Y., Jia, Y., Nishida, J., Wang, Z., Bunting, K. D., Wang, D. et al., IL-3 induces basophil expansion in vivo by directing granulocyte-monocyte progenitors to differentiate into basophil lineage-restricted progenitors in the bone marrow and by increasing the number of basophil/mast cell progenitors in the spleen. J. Immunol. 2009. 182: 28352841.
  • 14
    Lantz, C. S., Boesiger, J., Song, C. H., Mach, N., Kobayashi, T., Mulligan, R. C., Nawa, Y. et al., Role for interleukin-3 in mast-cell and basophil development and in immunity to parasites. Nature 1998. 392: 9093.
  • 15
    Shen, T., Kim, S., Do, J. S., Wang, L., Lantz, C., Urban, J. F., Le Gros, G. et al., T cell-derived IL-3 plays key role in parasite infection-induced basophil production but is dispensable for in vivo basophil survival. Int. Immunol. 2008. 20: 12011209.
  • 16
    Geijsen, N., Koenderman, L. and Coffer, P. J., Specificity in cytokine signal transduction: lessons learned from the IL-3/IL-5/GM-CSF receptor family. Cytokine Growth Factor Rev. 2001. 12: 1925.
  • 17
    Stomski, F. C., Woodcock, J. M., Zacharakis, B., Bagley, C. J., Sun, Q. and Lopez, A. F., Identification of a Cys motif in the common beta chain of the interleukin 3, granulocyte-macrophage colony-stimulating factor, and interleukin 5 receptors essential for disulfide-linked receptor heterodimerization and activation of all three receptors. J. Biol. Chem. 1998. 273: 11921199.
  • 18
    Mui, A. L., Wakao, H., O'Farrell, A. M., Harada, N. and Miyajima, A., Interleukin-3, granulocyte-macrophage colony stimulating factor and interleukin-5 transduce signals through two STAT5 homologs. EMBO J. 1995. 14: 11661175.
  • 19
    Hansen, G., Hercus, T. R., McClure, B. J., Stomski, F. C., Dottore, M., Powell, J., Ramshaw, H. et al., The structure of the GM-CSF receptor complex reveals a distinct mode of cytokine receptor activation. Cell 2008. 134: 496507.
  • 20
    Hara, T. and Miyajima, A., Two distinct functional high affinity receptors for mouse interleukin-3 (IL-3). EMBO J. 1992. 11: 18751884.
  • 21
    Schneider, E., Petit-Bertron, A. F., Bricard, R., Levasseur, M., Ramadan, A., Girard, J. P., Herbelin, A. et al., IL-33 activates unprimed murine basophils directly in vitro and induces their in vivo expansion indirectly by promoting hematopoietic growth factor production. J. Immunol. 2009. 183: 35913597.
  • 22
    Didichenko, S. A., Spiegl, N., Brunner, T. and Dahinden, C. A., IL-3 induces a Pim1-dependent antiapoptotic pathway in primary human basophils. Blood 2008. 112: 39493958.
  • 23
    Zheng, X., Karsan, A., Duronio, V., Chu, F., Walker, D. C., Bai, T. R. and Schellenberg, R. R., Interleukin-3, but not granulocyte-macrophage colony-stimulating factor and interleukin-5, inhibits apoptosis of human basophils through phosphatidylinositol 3-kinase: requirement of NF-kappaB-dependent and -independent pathways. Immunology 2002. 107: 306315.
  • 24
    Ochensberger, B., Tassera, L., Bifrare, D., Rihs, S. and Dahinden, C. A., Regulation of cytokine expression and leukotriene formation in human basophils by growth factors, chemokines and chemotactic agonists. Eur. J. Immunol. 1999. 29: 1122.
  • 25
    Perrigoue, J. G., Saenz, S. A., Siracusa, M. C., Allenspach, E. J., Taylor, B. C., Giacomin, P. R., Nair, M. G. et al., MHC class II-dependent basophil-CD4+ T-cell interactions promote T(H)2 cytokine-dependent immunity. Nat. Immunol. 2009. 10: 697705.
  • 26
    Sims, J. E., Williams, D. E., Morrissey, P. J., Garka, K., Foxworthe, D., Price, V., Friend, S. L. et al., Molecular cloning and biological characterization of a novel murine lymphoid growth factor. J. Exp. Med. 2000. 192: 671680.
  • 27
    Pandey, A., Ozaki, K., Baumann, H., Levin, S. D., Puel, A., Farr, A. G., Ziegler, S. F. et al., Cloning of a receptor subunit required for signaling by thymic stromal lymphopoietin. Nat. Immunol. 2000. 1: 5964.
  • 28
    Osborn, M. J., Ryan, P. L., Kirchhof, N., Panoskaltsis-Mortari, A., Mortari, F. and Tudor, K. S., Overexpression of murine TSLP impairs lymphopoiesis and myelopoiesis. Blood 2004. 103: 843851.
  • 29
    Schneider, E., Tonanny, M. B., Lisbonne, M., Leite-de-Moraes, M. and Dy, M., Pro-Th1 cytokines promote Fas-dependent apoptosis of immature peripheral basophils. J. Immunol. 2004. 172: 52625268.
  • 30
    Hida, S., Tadachi, M., Saito, T. and Taki, S., Negative control of basophil expansion by IRF-2 critical for the regulation of Th1/Th2 balance. Blood 2005. 106: 20112017.
  • 31
    Lagasse, E. and Weissman, I. L., bcl-2 inhibits apoptosis of neutrophils but not their engulfment by macrophages. J. Exp. Med. 1994. 179: 10471052.
  • 32
    Sokol, C. L., Chu, N. Q., Yu, S., Nish, S. A., Laufer, T. M. and Medzhitov, R., Basophils function as antigen-presenting cells for an allergen-induced T helper type 2 response. Nat. Immunol. 2009. 10: 713720.
  • 33
    Lilla, J. N., Chen, C. C., Mukai, K., Benbarak, M. J., Franco, C. B., Kalesnikoff, J., Yu, M. et al., Reduced mast cell and basophil numbers and function in Cpa3-Cre; Mcl-1fl/fl mice. Blood 2011. 118: 6930-6938.
  • 34
    Kim, S., Prout, M., Ramshaw, H., Lopez, A. F., LeGros, G. and Min, B., Cutting edge: basophils are transiently recruited into the draining lymph nodes during helminth infection via IL-3, but infection-induced Th2 immunity can develop without basophil lymph node recruitment or IL-3. J. Immunol. 2010. 184: 11431147.
  • 35
    Suzukawa, M., Iikura, M., Koketsu, R., Nagase, H., Tamura, C., Komiya, A., Nakae, S. et al., An IL-1 cytokine member, IL-33, induces human basophil activation via its ST2 receptor. J. Immunol. 2008. 181: 59815989.
  • 36
    Qi, X., Nishida, J., Chaves, L., Ohmori, K. and Huang, H., CCAAT/enhancer-binding protein alpha (C/EBPalpha) is critical for interleukin-4 expression in response to FcepsilonRI receptor cross-linking. J. Biol. Chem. 2011. 286: 1606316073.
  • 37
    Hida, S., Yamasaki, S., Sakamoto, Y., Takamoto, M., Obata, K., Takai, T., Karasuyama, H. et al., Fc receptor gamma-chain, a constitutive component of the IL-3 receptor, is required for IL-3-induced IL-4 production in basophils. Nat. Immunol. 2009. 10: 214222.
  • 38
    Barnstein, B. O., Li, G., Wang, Z., Kennedy, S., Chalfant, C., Nakajima, H., Bunting, K. D. et al., Stat5 expression is required for IgE-mediated mast cell function. J. Immunol. 2006. 177: 34213426.
  • 39
    Rathinam, V. A., Vanaja, S. K. and Fitzgerald, K. A., Regulation of inflammasome signaling. Nat. Immunol. 2012. 13: 333332.
  • 40
    Dinarello, C. A., The IL-1 family and inflammatory diseases. Clin. Exp. Rheumatol. 2002. 20: S113.
  • 41
    Hoshino, T., Yagita, H., Ortaldo, J. R., Wiltrout, R. H. and Young, H. A., In vivo administration of IL-18 can induce IgE production through Th2 cytokine induction and up-regulation of CD40 ligand (CD154) expression on CD4 +T cells. Eur. J. Immunol. 2000. 30: 19982006.
  • 42
    Yoshimoto, T., Tsutsui, H., Tominaga, K., Hoshino, K., Okamura, H., Akira, S., Paul, W. E. et al., IL-18, although antiallergic when administered with IL-12, stimulates IL-4 and histamine release by basophils. Proc. Natl. Acad. Sci. USA 1999. 96: 1396213966.
  • 43
    Zaitsu, M., Yamasaki, F., Ishii, E., Midoro-Horiuti, T., Goldblum, R. M. and Hamasaki, Y., Interleukin-18 primes human basophilic KU812 cells for higher leukotriene synthesis. Prostaglandins Leukot. Essent. Fatty Acids 2006. 74: 6166.
  • 44
    Pecaric-Petkovic, T., Didichenko, S. A., Kaempfer, S., Spiegl, N. and Dahinden, C. A., Human basophils and eosinophils are the direct target leukocytes of the novel IL-1 family member IL-33. Blood 2009. 113: 15261534.
  • 45
    Voehringer, D., Shinkai, K. and Locksley, R. M., Type 2 immunity reflects orchestrated recruitment of cells committed to IL-4 production. Immunity 2004. 20: 267277.
  • 46
    Liew, F. Y., Pitman, N. I. and McInnes, I. B., Disease-associated functions of IL-33: the new kid in the IL-1 family. Nat. Rev. Immunol. 2010. 10: 103110.
  • 47
    Smithgall, M. D., Comeau, M. R., Yoon, B. R., Kaufman, D., Armitage, R. and Smith, D. E., IL-33 amplifies both Th1- and Th2-type responses through its activity on human basophils, allergen-reactive Th2 cells, iNKT and NK cells. Int. Immunol. 2008. 20: 10191030.
  • 48
    Blom, L., Poulsen, B. C., Jensen, B. M., Hansen, A. and Poulsen, L. K., IL-33 induces IL-9 production in human CD4+ T cells and basophils. PLoS One 2011. 6: e21695.
  • 49
    Suzukawa, M., Nagase, H., Ogahara, I., Han, K., Tashimo, H., Shibui, A., Koketsu, R. et al., Leptin enhances survival and induces migration, degranulation, and cytokine synthesis of human basophils. J. Immunol. 2011. 186: 52545260.
  • 50
    Xu, D., Chan, W. L., Leung, B. P., Huang, F., Wheeler, R., Piedrafita, D., Robinson, J. H. et al., Selective expression of a stable cell surface molecule on type 2 but not type 1 helper T cells. J. Exp. Med. 1998. 187: 787794.
  • 51
    Bonilla, W. V., Frohlich, A., Senn, K., Kallert, S., Fernandez, M., Johnson, S., Kreutzfeldt, M. et al., The alarmin interleukin-33 drives protective antiviral CD8 T-cell responses. Science 2012. 335: 984989.
  • 52
    Hayakawa, H., Hayakawa, M., Kume, A. and Tominaga, S., Soluble ST2 blocks interleukin-33 signaling in allergic airway inflammation. J. Biol. Chem. 2007. 282: 2636926380.
  • 53
    Palmer, G. and Gabay, C., Interleukin-33 biology with potential insights into human diseases. Nat. Rev. Rheumatol. 2011. 7: 321329.
  • 54
    Kuroda, E., Antignano, F., Ho, V. W., Hughes, M. R., Ruschmann, J., Lam, V., Kawakami, T. et al., SHIP represses Th2 skewing by inhibiting IL-4 production from basophils. J. Immunol. 2011. 186: 323332.
  • 55
    Charles, N., Watford, W. T., Ramos, H. L., Hellman, L., Oettgen, H. C., Gomez, G., Ryan, J. J. et al., Lyn kinase controls basophil GATA-3 transcription factor expression and induction of Th2 cell differentiation. Immunity 2009. 30: 533543.
  • 56
    Peltola, K. J., Paukku, K., Aho, T. L., Ruuska, M., Silvennoinen, O. and Koskinen, P. J., Pim-1 kinase inhibits STAT5-dependent transcription via its interactions with SOCS1 and SOCS3. Blood 2004. 103: 37443750.
  • 57
    Matsumoto, A., Masuhara, M., Mitsui, K., Yokouchi, M., Ohtsubo, M., Misawa, H., Miyajima, A. et al., CIS, a cytokine inducible SH2 protein, is a target of the JAK-STAT5 pathway and modulates STAT5 activation. Blood 1997. 89: 31483154.
  • 58
    Yoshimura, A., Naka, T. and Kubo, M., SOCS proteins, cytokine signalling and immune regulation. Nat. Rev. Immunol. 2007. 7: 454465.