Your browser doesn't support javascript.
loading
Requirement for Tec kinases Rlk and Itk in T cell receptor signaling and immunity.
Schaeffer, E M; Debnath, J; Yap, G; McVicar, D; Liao, X C; Littman, D R; Sher, A; Varmus, H E; Lenardo, M J; Schwartzberg, P L.
  • Schaeffer EM; National Human Genome Research Institute, National Cancer Institute, National Institute for Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Science ; 284(5414): 638-41, 1999 Apr 23.
Article en En | MEDLINE | ID: mdl-10213685
ABSTRACT
T cell receptor (TCR) signaling requires activation of Zap-70 and Src family tyrosine kinases, but requirements for other tyrosine kinases are less clear. Combined deletion in mice of two Tec kinases, Rlk and Itk, caused marked defects in TCR responses including proliferation, cytokine production, and apoptosis in vitro and adaptive immune responses to Toxoplasma gondii in vivo. Molecular events immediately downstream from the TCR were intact in rlk-/-itk-/- cells, but intermediate events including inositol trisphosphate production, calcium mobilization, and mitogen-activated protein kinase activation were impaired, establishing Tec kinases as critical regulators of TCR signaling required for phospholipase C-gamma activation.
Asunto(s)
Search on Google
Banco de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Receptores de Antígenos de Linfocitos T / Linfocitos T / Transducción de Señal Límite: Animals Idioma: En Año: 1999 Tipo del documento: Article
Search on Google
Banco de datos: MEDLINE Asunto principal: Proteínas Tirosina Quinasas / Receptores de Antígenos de Linfocitos T / Linfocitos T / Transducción de Señal Límite: Animals Idioma: En Año: 1999 Tipo del documento: Article