Helvering L M, Richardson K K, Horn D M, Wightman K A, Hall R L, Smith W C, Engelhardt J A, Richardson F C
Toxicology Research Laboratories, Lilly Research Laboratories (a Division of Eli Lilly and Company), Greenfield, Indiana 46140.
Cancer Lett. 1993 Jul 30;71(1-3):133-42. doi: 10.1016/0304-3835(93)90108-l.
Increased message levels of testosterone-repressed prostate message-2 (TRPM-2) have been associated with programmed cell death in many tissues. To study its involvement in the apoptotic elimination of hepatocytes during liver involution and regeneration, levels of TRPM-2 message were evaluated in situ and by the ribonuclease protection assay. Although significant increases in apoptotic bodies were observed in rats 96 h following treatment with lead nitrate and ethylene dibromide, an increase in TRPM-2 message was not detected. Therefore, the expression of TRPM-2 mRNA may be a poor indicator of the extent to which apoptosis occurs during liver involution.
睾酮抑制的前列腺信息-2(TRPM-2)的信息水平升高与许多组织中的程序性细胞死亡有关。为了研究其在肝脏退化和再生过程中对肝细胞凋亡消除的参与情况,通过原位和核糖核酸酶保护试验评估了TRPM-2信息的水平。尽管在用硝酸铅和二溴乙烷处理96小时后的大鼠中观察到凋亡小体显著增加,但未检测到TRPM-2信息的增加。因此,TRPM-2 mRNA的表达可能不是肝脏退化过程中凋亡发生程度的良好指标。