Green L G, Stein J L, Stein G S
Biochem Pharmacol. 1984 Apr 1;33(7):1033-40. doi: 10.1016/0006-2952(84)90510-0.
The influence of delta 9-tetrahydrocannabinol (delta 9-THC) on the cellular levels of histone mRNAs and ribosomal RNAs was examined in several normal and transformed human cell lines--HeLa S3 cells, WI-38 human diploid fibroblasts, SV40-transformed WI-38 cells, and A549 lung carcinoma cells. RNA sequences were quantitatively assayed by electrophoretic fractionation, transfer to nitrocellulose, and hybridization with cloned genomic human histone or ribosomal DNA sequences. Treatment with delta 9-THC (10-40 microM) for 10 hr resulted in a concentration-dependent decrease in the representation of H2A, H2B, H3 and H4 histone mRNAs without a significant inhibitory effect on the levels of ribosomal RNAs. The cannabinoid-mediated inhibitory effect on histone gene expression was less evident in cells with active drug-metabolizing systems.
在几种正常和转化的人类细胞系——HeLa S3细胞、WI-38人二倍体成纤维细胞、SV40转化的WI-38细胞和A549肺癌细胞中,研究了δ9-四氢大麻酚(δ9-THC)对组蛋白mRNA和核糖体RNA细胞水平的影响。通过电泳分离、转移至硝酸纤维素膜以及与克隆的基因组人类组蛋白或核糖体DNA序列杂交,对RNA序列进行定量分析。用δ9-THC(10-40微摩尔)处理10小时导致H2A、H2B、H3和H4组蛋白mRNA的表达呈浓度依赖性降低,而对核糖体RNA水平没有显著抑制作用。在具有活跃药物代谢系统的细胞中,大麻素介导的对组蛋白基因表达的抑制作用不太明显。