Mayumi-Matsuda K, Kojima S, Suzuki H, Sakata T
Shionogi Institute for Medical Science, 5-1, Mishima 2-chome, Settsu-shi, Osaka, 566-0022, Japan.
Biochem Biophys Res Commun. 1999 May 10;258(2):260-4. doi: 10.1006/bbrc.1999.0576.
When deprived of neurotrophic factors, neuronal cells undergo a form of programmed cell death that involves a cascade of gene expression. To better understand this cascade, we screened the genes induced during programmed cell death evoked in neuronal PC6-3 cells by NGF-depletion and discovered a novel gene, NIPK (Neuronal cell death Inducible Putative Kinase), that contains a kinase-like domain. Expression of NIPK was also induced in cultured sympathetic neurons by NGF deprivation and in cortical neurons exposed to the Ca2+ ionophore, A23187. In contrast, NIPK was not induced during non-neuronal cell death evoked by serum or growth factor deprivation, or by treatment with methyl methanesulfonate, an agent that causes cell death by damaging DNA. Taken together, these findings suggest that NIPK is involved in programmed cell death via a pathway that is present in neurons but is absent in non-neurons.
当神经元细胞被剥夺神经营养因子时,会经历一种程序性细胞死亡形式,这涉及一系列基因表达。为了更好地理解这一基因表达序列,我们筛选了在PC6-3神经元细胞中因NGF缺失诱发的程序性细胞死亡过程中诱导表达的基因,并发现了一个新基因NIPK(神经元细胞死亡诱导性假定激酶),它含有一个类激酶结构域。在培养的交感神经元中,NGF缺失也会诱导NIPK表达,在暴露于Ca2+离子载体A23187的皮质神经元中同样如此。相反,在血清或生长因子剥夺诱发的非神经元细胞死亡过程中,或者在用甲基磺酸甲酯(一种通过损伤DNA导致细胞死亡的试剂)处理时,NIPK不会被诱导表达。综上所述,这些发现表明,NIPK通过一种存在于神经元但不存在于非神经元中的途径参与程序性细胞死亡。