CEP-1347 (KT7515), a semisynthetic inhibitor of the mixed lineage kinase family

被引:189
作者
Maroney, AC
Finn, JP
Connors, TJ
Durkin, JT
Angeles, T
Gessner, G
Xu, ZH
Meyer, SL
Savage, MJ
Greene, LA
Scott, RW
Vaught, JL
机构
[1] Cephalon Inc, W Chester, PA 19380 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
D O I
10.1074/jbc.M011601200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CEP-1347 (KT7515) promotes neuronal survival at dosages that inhibit activation of the c-Jun amino-terminal kinases (JNKs) in primary embryonic cultures and differentiated PC12 cells after trophic withdrawal and in mice treated with 1-methyl-4-phenyl tetrahydropyridine. In an effort to identify molecular target(s) of CEP-1347 in the JNK cascade, JNK1 and known upstream regulators of JNK1 were co-expressed in Cos-7 cells to determine whether CEP-1347 could modulate JNK1 activation. CEP-1347 blocked JNK1 activation induced by members of the mixed lineage kinase (MLK) family (MLK3, MLK2, MLK1, dual leucine zipper kinase, and leucine zipper kinase), The response was selective because CEP-1347 did not inhibit JNK1 activation in cells induced by kinases independent of the MLK cascade. CEP-1347 inhibition of recombinant MLK members in vitro was competitive with ATP, resulting in IC,, values ranging from 23 to 51 nM, comparable to inhibitory potencies observed in intact cells. In addition, overexpression of MLK3 led to death in Chinese hamster ovary cells, and CEP-1347 blocked this death at doses comparable to those that inhibited MLK3 kinase activity. These results identify MLKs as targets of CEP-1347 in the JNK signaling cascade and demonstrate that CEP-1347 can block MLK-induced cell death.
引用
收藏
页码:25302 / 25308
页数:7
相关论文
共 76 条
[61]  
SANCHEZ I, 1994, NATURE, V372, P794, DOI 10.1038/372794a0
[62]   MPTP activates c-Jun NH2-terminal kinase (JNK) and its upstream regulatory kinase MKK4 in nigrostriatal neurons in vivo [J].
Saporito, MS ;
Thomas, BA ;
Scott, RW .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (03) :1200-1208
[63]   Preservation of cholinergic activity and prevention of neuron death by CEP-1347/KT-7515 following excitotoxic injury of the nucleus basalis magnocellularis [J].
Saporito, MS ;
Brown, ER ;
Carswell, S ;
DiCamillo, AM ;
Miller, MS ;
Murakata, C ;
Neff, NT ;
Vaught, JL ;
Haun, FA .
NEUROSCIENCE, 1998, 86 (02) :461-472
[64]  
Saporito MS, 1999, J PHARMACOL EXP THER, V288, P421
[65]   THE ROLE OF JUN TRANSCRIPTION FACTOR EXPRESSION AND PHOSPHORYLATION IN NEURONAL DIFFERENTIATION, NEURONAL CELL-DEATH, AND PLASTIC ADAPTATIONS IN-VIVO [J].
SCHLINGENSIEPEN, KH ;
WOLLNIK, F ;
KUNST, M ;
SCHLINGENSIEPEN, R ;
HERDEGEN, T ;
BRYSCH, W .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 1994, 14 (05) :487-505
[66]   SINGLE-STEP PURIFICATION OF POLYPEPTIDES EXPRESSED IN ESCHERICHIA-COLI AS FUSIONS WITH GLUTATHIONE S-TRANSFERASE [J].
SMITH, DB ;
JOHNSON, KS .
GENE, 1988, 67 (01) :31-40
[67]   Signaling from the small GTP-binding proteins Rac1 and Cdc42 to the c-Jun N-terminal kinase stress-activated protein kinase pathway - A role for mixed lineage kinase 3 protein-tyrosine kinase 1, a novel member of the mixed lineage kinase family [J].
Teramoto, H ;
Coso, OA ;
Miyata, H ;
Igishi, T ;
Miki, T ;
Gutkind, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) :27225-27228
[68]   The stress-activated protein kinase pathways [J].
Tibbles, LA ;
Woodgett, JR .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (10) :1230-1254
[69]   A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket [J].
Tong, L ;
Pav, S ;
White, DM ;
Rogers, S ;
Crane, KM ;
Cywin, CL ;
Brown, ML ;
Pargellis, CA .
NATURE STRUCTURAL BIOLOGY, 1997, 4 (04) :311-316
[70]   Mitogen-activated protein kinase kinase 7 is an activator of the c-Jun NH2-terminal kinase [J].
Tournier, C ;
Whitmarsh, AJ ;
Cavanagh, J ;
Barrett, T ;
Davis, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7337-7342