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Activation of p42/p44 mitogen‐activated protein kinases (MAPK) and p38 MAPK by tumor necrosis factor (TNF) is mediated through the death domain of the 55‐kDa TNF receptor
Author(s) -
Boone Elke,
Vandevoorde Veronique,
De Wilde Gert,
Haegeman Guy
Publication year - 1998
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(98)01567-1
Subject(s) - mapk/erk pathway , tumor necrosis factor alpha , p38 mitogen activated protein kinases , microbiology and biotechnology , mitogen activated protein kinase , kinase , tumor necrosis factor receptor , protein kinase a , chemistry , receptor , cancer research , biology , biochemistry , immunology
In the mouse fibrosarcoma cell line L929sA, tumor necrosis factor (TNF) stimulates activation of the stress‐responsive p38 mitogen‐activated protein kinase (MAPK), as well as the classical p42 and p44 MAPK. TNF signaling can be mediated by p55 or p75 TNF receptors. Here, we demonstrate that TNF‐R55 is sufficient to activate p42/p44 MAPK and p38 MAPK. Moreover, by expressing different membrane‐bound or purely cytoplasmic truncations of TNF‐R55, we show that the intracellular death domain of TNF‐R55 is the crucial domain involved. The cytoplasmic membrane‐proximal region of TNF‐R55, known to induce neutral sphingomyelinase activation, is not required for activation of p38 MAPK or p42/p44 MAPK.