Maroney A C, Finn J P, Connors T J, Durkin J T, Angeles T, Gessner G, Xu Z, Meyer S L, Savage M J, Greene L A, Scott R W, Vaught J L
Cephalon Inc., 145 Brandywine Pkwy., West Chester, Pennsylvania 19380, USA.
J Biol Chem. 2001 Jul 6;276(27):25302-8. doi: 10.1074/jbc.M011601200. Epub 2001 Apr 26.
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(50) 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.
CEP - 1347(KT7515)在原代胚胎培养物以及营养因子撤除后的分化PC12细胞中,以及在用1 - 甲基 - 4 - 苯基四氢吡啶处理的小鼠中,以抑制c - Jun氨基末端激酶(JNKs)激活的剂量促进神经元存活。为了确定CEP - 1347在JNK级联反应中的分子靶点,将JNK1和已知的JNK1上游调节因子在Cos - 7细胞中共表达,以确定CEP - 1347是否能调节JNK1的激活。CEP - 1347阻断了混合谱系激酶(MLK)家族成员(MLK3、MLK2、MLK1、双亮氨酸拉链激酶和亮氨酸拉链激酶)诱导的JNK1激活。这种反应具有选择性,因为CEP - 1347不会抑制由独立于MLK级联反应的激酶诱导的细胞中的JNK1激活。CEP - 1347在体外对重组MLK成员的抑制作用与ATP具有竞争性,导致IC(50)值在23至51纳米之间,与在完整细胞中观察到的抑制效力相当。此外,MLK3的过表达导致中国仓鼠卵巢细胞死亡,而CEP - 1347以与抑制MLK3激酶活性相当的剂量阻断了这种死亡。这些结果确定MLKs是JNK信号级联反应中CEP - 1347的靶点,并证明CEP - 1347可以阻断MLK诱导的细胞死亡。