Zhang X, Kiechle F L
Department of Clinical Pathology, William Beaumont Hospital, Royal Oak, MI 48073, USA.
Ann Clin Lab Sci. 1998 Mar-Apr;28(2):104-14.
Hoechst 33342, a bisbenzimidazole dye, binds to adenine/thymine rich regions in the minor groove of deoxyribonucleic acid (DNA). This dye induces apoptosis in BC3H-1 myocytes. The mechanism of Hoechst 33342-induced apoptosis was investigated. Inhibitors of ribonucleic acid (RNA) synthesis, protein synthesis, and serine or cysteine proteases failed to prevent BC3H-1 myocyte death induced by Hoechst 33342. Apoptosis may be dependent on increased p53 expression. Hoechst 33342 had no effect on p53 expression in BC3H-1 myocytes. Lactate oxidation, a monitor of mitochondrial function, was altered by Hoechst 33342 in dose dependent manner. Also, nuclear extracts were used to assay endogenous topoisomerase I activity which was inhibited by Hoechst 33342 treatment of BC3H-1 myocytes. Therefore, Hoechst 33342 appears to initiate apoptosis in BC3H-1 myocytes by a pathway which is independent of de novo RNA and protein synthesis. However, the dye does initiate mitochondrial dysfunction and inhibition of nuclear topoisomerase I as two important steps in the apoptotic pathway.
Hoechst 33342是一种双苯并咪唑染料,可与脱氧核糖核酸(DNA)小沟中富含腺嘌呤/胸腺嘧啶的区域结合。这种染料可诱导BC3H-1心肌细胞凋亡。研究了Hoechst 33342诱导凋亡的机制。核糖核酸(RNA)合成抑制剂、蛋白质合成抑制剂以及丝氨酸或半胱氨酸蛋白酶均无法阻止Hoechst 33342诱导的BC3H-1心肌细胞死亡。凋亡可能依赖于p53表达的增加。Hoechst 33342对BC3H-1心肌细胞中的p53表达没有影响。乳酸氧化作为线粒体功能的一个监测指标,被Hoechst 33342以剂量依赖的方式改变。此外,使用核提取物检测内源性拓扑异构酶I的活性,Hoechst 33342处理BC3H-1心肌细胞可抑制该活性。因此,Hoechst 33342似乎通过一条独立于从头RNA和蛋白质合成的途径引发BC3H-1心肌细胞凋亡。然而,这种染料确实引发了线粒体功能障碍和核拓扑异构酶I的抑制,这是凋亡途径中的两个重要步骤。