Nakatsukasa H, Silverman J A, Gant T W, Evarts R P, Thorgeirsson S S
Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-0037.
Hepatology. 1993 Nov;18(5):1202-7.
We analyzed expression of multidrug resistance (mdr) genes in rat liver during regeneration after partial hepatectomy or carbon tetrachloride-induced necrosis. In situ hybridization revealed that in the normal liver the cellular distribution of mdr transcripts and protein is restricted to hepatocytes and that a gradient, highest in zone 1 and lowest in zone 3, exists in the level of the mdr transcripts in the liver acinus. Increased levels of mdr1a and mdr1b transcripts were observed 3 hr after administration of carbon tetrachloride and remained increased for the next 5 days. In contrast, increased expression of mdr1a and mdr1b was first observed 24 hr after partial hepatectomy. Use of gene-specific probes to compare the time courses of mdr1b and mdr2 expression after carbon tetrachloride administration showed distinctly different patterns of expression; mdr1b reached a maximum level of expression at 12 hr, whereas increased mdr2 expression was first observed 48 hr after administration. Nuclear run-on analysis at 12 and 24 hr after carbon tetrachloride administration demonstrated 10-fold and eightfold increases in mdr transcription, respectively. However, 72 hr after carbon tetrachloride treatment the rate of mdr transcription was back to the control level. The cellular patterns of mdr expression after partial hepatectomy and carbon tetrachloride administration were similar; the increase was first observed in zone 1 and gradually extended into zone 3. These data strongly suggest that the physiological roles of mdr1b and mdr2 are different and that liver regeneration is an appropriate model for elucidating these differences.
我们分析了部分肝切除或四氯化碳诱导坏死术后大鼠肝脏再生过程中多药耐药(mdr)基因的表达。原位杂交显示,在正常肝脏中,mdr转录本和蛋白的细胞分布仅限于肝细胞,并且肝腺泡中mdr转录本水平存在梯度,1区最高,3区最低。给予四氯化碳3小时后观察到mdr1a和mdr1b转录本水平升高,并在接下来的5天内持续升高。相比之下,部分肝切除术后24小时首次观察到mdr1a和mdr1b表达增加。使用基因特异性探针比较四氯化碳给药后mdr1b和mdr2表达的时间进程,显示出明显不同的表达模式;mdr1b在12小时达到最大表达水平,而mdr2表达增加在给药后48小时首次观察到。四氯化碳给药后12小时和24小时的核转录分析分别显示mdr转录增加了10倍和8倍。然而,四氯化碳处理72小时后,mdr转录速率恢复到对照水平。部分肝切除和四氯化碳给药后mdr表达的细胞模式相似;增加首先在1区观察到,并逐渐扩展到3区。这些数据强烈表明mdr1b和mdr2的生理作用不同,肝脏再生是阐明这些差异的合适模型。