The intracellular signal transduction mechanism of interleukin 5 in eosinophils: the involvement of lyn tyrosine kinase and the Ras-Raf-1- MEK-microtubule-associated protein kinase pathway

Interleukin 5 (IL-5) regulates the growth and function of eosinophils. The objective of this study was to investigate the intracellular signal transduction mechanism of IL-5 in eosinophils. Purified eosinophils were stimulated with IL-5, and the involvement of various kinases was investigated by immunoblotting, immune complex kinase assay, and in situ denatured/renatured kinase assay. We found that IL-5 induced tyrosine phosphorylation and activation of a number of kinases. Two species of lyn kinases (53 and 56 kD) were present in eosinophils. Both forms were Tyr-phosphorylated and activated rapidly within 1 min. Further, lyn kinase was physically associated with the IL-5 beta receptor in eosinophils. Ras was studied by immunoprecipitation followed by thin-layer chromatography. Ras bound higher quantities of [alpha-32P]guanosine 5'triphosphate upon stimulation with IL-5. Raf-1 kinase showed increased Tyr phosphorylation on immunoblotting and increased activity in the immune complex kinase assay. Two species of MEK (MAP or Erk kinase) (41 and 45 kD) were identified in eosinophils, which underwent autophosphorylation upon stimulation. Microtubule- associated protein (MAP) kinase (p44) was Tyr-phosphorylated on immunoblotting and had increased activity in the immune-complex kinase assay. MAP kinases were also studied after metabolic radiolabeling of the cells with [32P]orthophosphates. IL-5 stimulated phosphorylation of MAP kinases in situ. Thus, we have delineated major components of an important signaling pathway in eosinophils. We believe that one of the signals generated by IL-5 receptor activation is propagated through the lyn-Ras-Raf-1-MEK-MAP kinase pathway.

[1]  T. Watanabe,et al.  IL-5 receptor-mediated tyrosine phosphorylation of SH2/SH3-containing proteins and activation of Bruton's tyrosine and Janus 2 kinases , 1994, The Journal of experimental medicine.

[2]  D. Templeton,et al.  Identification of 2 serine residues of MEK-1 that are differentially phosphorylated during activation by raf and MEK kinase. , 1994, The Journal of biological chemistry.

[3]  E. Reinherz,et al.  Delineation of a T-cell activation motif required for binding of protein tyrosine kinases containing tandem SH2 domains. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[4]  J. Hancock,et al.  Activation of Raf as a result of recruitment to the plasma membrane. , 1994, Science.

[5]  S. Corey,et al.  Granulocyte colony-stimulating factor receptor signaling involves the formation of a three-component complex with Lyn and Syk protein-tyrosine kinases. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J. Woodgett,et al.  The stress-activated protein kinase subfamily of c-Jun kinases , 1994, Nature.

[7]  J. Jongstra,et al.  Distinct p53/56lyn and p59fyn domains associate with nonphosphorylated and phosphorylated Ig-alpha. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[8]  J. Avruch,et al.  Enzymatic characteristics of the c-Raf-1 protein kinase. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[9]  J. Cambier,et al.  B cell antigen receptor cross-linking triggers rapid protein kinase C independent activation of p21ras1. , 1993, Journal of immunology.

[10]  K. Arai,et al.  Signal transduction by the high‐affinity GM‐CSF receptor: two distinct cytoplasmic regions of the common beta subunit responsible for different signaling. , 1993, The EMBO journal.

[11]  J. Sedivy,et al.  Raf-1 protein kinase activates the NF-kappa B transcription factor by dissociating the cytoplasmic NF-kappa B-I kappa B complex. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Walter Kolch,et al.  Protein kinase Cα activates RAF-1 by direct phosphorylation , 1993, Nature.

[13]  T. Roberts,et al.  Raf-1 and p21v-ras cooperate in the activation of mitogen-activated protein kinase. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[14]  K. Guan,et al.  Cloning and characterization of two distinct human extracellular signal-regulated kinase activator kinases, MEK1 and MEK2. , 1993, The Journal of biological chemistry.

[15]  L. Feig The many roads that lead to Ras. , 1993, Science.

[16]  T. Pawson,et al.  The SH2 and SH3 domains of mammalian Grb2 couple the EGF receptor to the Ras activator mSos1 , 1993, Nature.

[17]  C. Lange-Carter,et al.  A divergence in the MAP kinase regulatory network defined by MEK kinase and Raf , 1993, Science.

[18]  P. Forsythe,et al.  RANTES is a chemotactic and activating factor for human eosinophils. , 1993, Journal of immunology.

[19]  J. Lammers,et al.  Cytokine priming of the respiratory burst in human eosinophils is Ca2+ independent and accompanied by induction of tyrosine kinase activity , 1993, Journal of leukocyte biology.

[20]  J. Gomez-Cambronero,et al.  Direct stimulation by tyrosine phosphorylation of microtubule-associated protein (MAP) kinase activity by granulocyte-macrophage colony-stimulating factor in human neutrophils. , 1993, The Biochemical journal.

[21]  J. Saklatvala,et al.  The chemotactic factor N-formylmethionyl-leucyl-phenylalanine activates microtubule-associated protein 2 (MAP) kinase and a MAP kinase kinase in polymorphonuclear leucocytes. , 1993, The Biochemical journal.

[22]  T. Kawakami,et al.  Activation of Multiple Protein Kinases Including a MAP Kinase upon FcεRI Cross-Linking , 1993 .

[23]  J. Lin,et al.  The MB-1/B29 heterodimer couples the B cell antigen receptor to multiple src family protein tyrosine kinases. , 1992, Journal of immunology.

[24]  V. Duronio,et al.  Multiple hemopoietic growth factors stimulate activation of mitogen-activated protein kinase family members. , 1992, Journal of immunology.

[25]  K. Togawa,et al.  The effect of recombinant human interleukin-5 on eosinophil accumulation and degranulation in human nasal mucosa. , 1992, The Journal of allergy and clinical immunology.

[26]  John Calvin Reed,et al.  Interleukin-3 regulates the activity of the LYN protein-tyrosine kinase in myeloid-committed leukemic cell lines. , 1992, Blood.

[27]  Sheila M. Thomas,et al.  Ras is essential for nerve growth factor- and phorbol ester-induced tyrosine phosphorylation of MAP kinases , 1992, Cell.

[28]  G. Thomas MAP kinase by any other name smells just as sweet , 1992, Cell.

[29]  M. Vadas,et al.  GM-CSF, IL-3 and IL-5: cross-competition on human haemopoietic cells. , 1992, Immunology today.

[30]  M. Nakafuku,et al.  Involvement of ras p21 protein in signal-transduction pathways from interleukin 2, interleukin 3, and granulocyte/macrophage colony-stimulating factor, but not from interleukin 4. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[31]  I. Clark-lewis,et al.  Interleukin-3 and granulocyte-macrophage colony-stimulating factor mediate rapid phosphorylation and activation of cytosolic c-raf. , 1990, The Journal of biological chemistry.

[32]  M. Strath,et al.  Eosinophilia in transgenic mice expressing interleukin 5 , 1990, The Journal of experimental medicine.

[33]  J. Bousquet,et al.  Eosinophilic inflammation in asthma. , 1990, The New England journal of medicine.

[34]  D. Morrison,et al.  Direct activation of the serine/threonine kinase activity of raf-1 through tyrosine phosphorylation by the PDGF β-receptor , 1989, Cell.

[35]  R. Coffman,et al.  Antibody to interleukin-5 inhibits helminth-induced eosinophilia in mice. , 1989, Science.

[36]  T. Suda,et al.  Purified interleukin 5 supports the terminal differentiation and proliferation of murine eosinophilic precursors , 1988, The Journal of experimental medicine.

[37]  I. Gärtner Separation of human eosinophils in density gradients of polyvinylpyrrolidone-coated silica gel (Percoll). , 1980, Immunology.