Nishimura K, Tanuma S
Department of Biochemistry, Faculty of Pharmaceutical Sciences, Science University of Tokyo, Shinjuku-ku, Tokyo, Japan.
Apoptosis. 1998 Mar;3(2):97-103. doi: 10.1023/a:1009644924530.
DNase gamma, which cleaves chromosomal DNA into nucleosomal units (DNA ladder formation), has been suggested to be the critical component of apoptotic machinery. Using rat pheochromocytoma PC12 cells, which are differentiated to sympathetic neurons by nerve growth factor (NGF), we investigated whether DNase gamma-like enzyme is present in neuronal cells and is involved in neuronal cell death. The nuclear auto-digestion assay for DNase catalyzing internucleosomal DNA cleavage revealed that nuclei from neuronal differentiated PC12 cells contain acidic and neutral endonucleases, while nuclei from undifferentiated PC12 cells have only acidic endonuclease. The DNA ladder formation observed in isolated nuclei from neuronal differentiated PC12 cells at neutral pH requires both Ca(2+) and Mg(2+), and is sensitive to Zn(2+). The molecular mass of the neutral endonuclease present in neuronal differentiated PC12 cell nuclei is 32000 as determined by activity gel analysis (zymography). The properties of the neuronal endonuclease present in neuronal differentiated PC12 cell nuclei were similar to those of purified DNase gamma from rat thymocytes and splenocytes. Interestingly, in neuronal differentiated PC12 cells, internucleosomal DNA fragmentation is observed following NGF deprivation, whereas undifferentiated PC12 cells fail to exhibit DNA ladder formation during cell death by serum starvation. These results suggest that the DNase gamma-like endonuclease present in neuronal differentiated PC12 cell nuclei is involved in internucleosomal DNA fragmentation during apoptosis, induced by NGF deprivation.
脱氧核糖核酸酶γ可将染色体DNA切割成核小体单位(形成DNA梯状条带),被认为是凋亡机制的关键组成部分。我们使用经神经生长因子(NGF)诱导分化为交感神经元的大鼠嗜铬细胞瘤PC12细胞,研究神经元细胞中是否存在类似脱氧核糖核酸酶γ的酶以及该酶是否参与神经元细胞死亡。针对催化核小体间DNA切割的脱氧核糖核酸酶的核自消化分析显示,分化后的神经元PC12细胞核含有酸性和中性核酸内切酶,而未分化的PC12细胞核仅含有酸性核酸内切酶。在中性pH条件下,从分化后的神经元PC12细胞分离出的细胞核中观察到的DNA梯状条带形成需要Ca(2+)和Mg(2+),并且对Zn(2+)敏感。通过活性凝胶分析(酶谱法)测定,分化后的神经元PC12细胞核中存在的中性核酸内切酶的分子量为32000。分化后的神经元PC12细胞核中存在的神经元核酸内切酶的特性与从大鼠胸腺细胞和脾细胞中纯化得到的脱氧核糖核酸酶γ相似。有趣的是,在分化后的神经元PC12细胞中,NGF剥夺后可观察到核小体间DNA片段化,而未分化的PC12细胞在血清饥饿诱导的细胞死亡过程中未能表现出DNA梯状条带形成。这些结果表明,分化后的神经元PC12细胞核中存在的类似脱氧核糖核酸酶γ的核酸内切酶参与了NGF剥夺诱导的凋亡过程中的核小体间DNA片段化。