Aihara Koutoku, Kuroda Shun'ichi, Kanayama Norihiro, Matsuyama Shogo, Tanizawa Katsuyuki, Horie Masato
Second Institute of New Drug Discovery, Otsuka Pharmaceutical Co Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima 771-0192, Japan.
Brain Res Mol Brain Res. 2003 Aug 19;116(1-2):86-93. doi: 10.1016/s0169-328x(03)00256-0.
NELL2 is a neuron-specific thrombospondin-1-like extracellular protein containing six epidermal growth factor-like domains. NELL2 is highly expressed in the hippocampus and cerebral cortex. Although the involvement of NELL2 in neural functions has been inferred from its expression and biochemical profiles, biological roles of NELL2 remain uncertain. We evaluated the survival effect of NELL2 using primary cultured neurons from fetal rat brain following treatment with a recombinant NELL2 protein. NELL2 increased survival of neurons from the hippocampus and cerebral cortex. We further examined the protective effect of NELL2 from oxygen-glucose deprivation- and beta-amyloid-induced neuronal death, and found that NELL2 did not protect neurons from these insults. To understand signaling properties underlying the survival effect, we studied activation of mitogen-activated protein kinases (MAPKs) by NELL2. Treatment of primary cultured cells from the hippocampus with NELL2 enhanced phosphorylation of c-jun N-terminal kinase (JNK), whereas phosphorylation of extracellular signal-regulated kinase (ERK) was decreased by NELL2 treatment. NELL2-enhanced survival of hippocampal neurons was completely blocked by SP600125, an anthrapyrazolone inhibitor of JNK, while treatment of MEK (MAPK/ERK kinase) inhibitors per se enhanced survival of neurons similar to NELL2 treatment. These results suggest that NELL2 promotes survival of neurons by modulating MAPK activities.
NELL2是一种神经元特异性的血小板反应蛋白-1样细胞外蛋白,含有六个表皮生长因子样结构域。NELL2在海马体和大脑皮层中高度表达。尽管已从其表达和生化特征推断出NELL2参与神经功能,但NELL2的生物学作用仍不确定。我们使用重组NELL2蛋白处理来自胎鼠大脑的原代培养神经元,评估了NELL2的存活效应。NELL2增加了海马体和大脑皮层神经元的存活率。我们进一步研究了NELL2对氧糖剥夺和β-淀粉样蛋白诱导的神经元死亡的保护作用,发现NELL2不能保护神经元免受这些损伤。为了了解存活效应背后的信号特性,我们研究了NELL2对丝裂原活化蛋白激酶(MAPK)的激活作用。用NELL2处理海马体的原代培养细胞可增强c-jun氨基末端激酶(JNK)的磷酸化,而NELL2处理则降低细胞外信号调节激酶(ERK)的磷酸化。JNK的蒽吡唑啉酮抑制剂SP600125完全阻断了NELL2增强的海马神经元存活率,而MEK(MAPK/ERK激酶)抑制剂本身的处理增强了神经元的存活率,类似于NELL2处理。这些结果表明,NELL2通过调节MAPK活性促进神经元存活。