TY - JOUR
T1 - The p75 neurotrophin receptor interacts with multiple MAGE proteins
AU - Tcherpakov, Marianna
AU - Bronfman, Francisca C.
AU - Conticello, Silvestro G.
AU - Vaskovsky, Anna
AU - Levy, Zehava
AU - Niinobe, Michio
AU - Yoshikawa, Kazuaki
AU - Arenas, Ernest
AU - Fainzilber, Mike
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2002/12/20
Y1 - 2002/12/20
N2 - The p75 neurotrophin receptor has been implicated in diverse aspects of neurotrophin signaling, but the mechanisms by which its effects are mediated are not well understood. Here we identify two MAGE proteins, necdin and MAGE-H1, as interactors for the intracellular domain of p75 and show that the interaction is enhanced by ligand stimulation. PC12 cells transfected with necdin or MAGE-H1 exhibit accelerated differentiation in response to nerve growth factor. Expression of these two MAGE proteins is predominantly cytoplasmic in PC12 cells, and needin was found to be capable of homodimerization, suggesting that it may act as a cytoplasmic adaptor to recruit a signaling complex to p75. These findings indicate that diverse MAGE family members can interact with the p75 receptor and highlight type II MAGE proteins as a potential family of interactors for signaling proteins containing type II death domains.
AB - The p75 neurotrophin receptor has been implicated in diverse aspects of neurotrophin signaling, but the mechanisms by which its effects are mediated are not well understood. Here we identify two MAGE proteins, necdin and MAGE-H1, as interactors for the intracellular domain of p75 and show that the interaction is enhanced by ligand stimulation. PC12 cells transfected with necdin or MAGE-H1 exhibit accelerated differentiation in response to nerve growth factor. Expression of these two MAGE proteins is predominantly cytoplasmic in PC12 cells, and needin was found to be capable of homodimerization, suggesting that it may act as a cytoplasmic adaptor to recruit a signaling complex to p75. These findings indicate that diverse MAGE family members can interact with the p75 receptor and highlight type II MAGE proteins as a potential family of interactors for signaling proteins containing type II death domains.
UR - http://www.scopus.com/inward/record.url?scp=0037147258&partnerID=8YFLogxK
U2 - 10.1074/jbc.C200533200
DO - 10.1074/jbc.C200533200
M3 - Article
C2 - 12414813
AN - SCOPUS:0037147258
SN - 0021-9258
VL - 277
SP - 49101
EP - 49104
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 51
ER -