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Complement regulatory protein Crry/p65‐mediated signaling in T lymphocytes: role of its cytoplasmic domain and partitioning into lipid rafts
Author(s) -
JiménezPeriañez Arturo,
Ojeda Gloria,
Criado Gabriel,
Sánchez Alejandra,
Pini Eliana,
Madrenas Joaquín,
Rojo Jose Maria,
Portolés Pilar
Publication year - 2005
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.1104642
Subject(s) - biology , lipid raft , complement (music) , microbiology and biotechnology , cytoplasm , complement system , signal transduction , domain (mathematical analysis) , immunology , immune system , biochemistry , gene , mathematical analysis , mathematics , complementation , phenotype
Crry/p65 is a type I glycoprotein, which protects mouse T cells from complement attack. We have previously shown that complement receptor I‐related protein Crry/p65 (Crry) ligation has a costimulatory effect on mouse CD4 + T cell activation. Here, we have examined the mechanisms responsible for Crry costimulation, addressing the question of whether Crry potentiates signal transduction starting at the T cell receptor (TCR)/CD3 complex or promotes distinct costimulatory signals. We show that Crry increases early TCR‐dependent activation signals, including p56 lck ‐, ζ‐associated protein‐70 (ZAP‐70), Vav‐1, Akt, and extracellular signal‐regulated kinase (ERK) phosphorylation but also costimulation‐dependent mitogen‐activated protein kinases (MAPK), such as the stress‐activated c‐Jun N‐terminal kinase (JNK). It is intriguing that Crry costimulus enhanced p38 MAPK activation in T helper cell type 1 (Th1) but not in Th2 cells. A fraction of Crry is found consistently in the detergent‐insoluble membrane fraction of Th1 or Th2 cells or CD4 + lymphoblasts. Crry costimulation induced clustering of lipid rafts, increasing their content in Crry, CD3ɛ, and p59‐60 forms of p56 lck , and caused actin polymerization close to the site of activation in Th2 cells. Such events were inhibited by wortmannin, suggesting a role for phosphatidylinositol‐3 kinase in these effects. The Crry cytoplasmic domain was required for JNK activation and interleukin‐4 secretion but not for the presence of Crry in rafts or activation of p56 lck , ZAP‐70, Akt, Vav‐1, or ERK. This suggests that Crry costimulation involves two different but not mutually exclusive signal transduction modules. The dual function of Crry as a complement regulatory protein and as a T cell costimulator illustrates the importance of complement regulatory proteins as links between innate and adaptive immunity.

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