Assy N, Gong Y, Zhang M, Pettigrew N M, Pashniak D, Minuk G Y
Department of Medicine, University of Manitoba, Health Sciences Centre, Winnipeg, Canada.
J Lab Clin Med. 1998 Mar;131(3):251-6. doi: 10.1016/s0022-2143(98)90097-x.
In order to document and compare proliferating cell nuclear antigen (PCNA) mRNA and protein levels with more traditional parameters of hepatic regenerative activity in a rat model, adult male Sprague-Dawley rats (4 to 6 per group) were killed at various times up to 96 hours after 70% partial hepatectomy. At each time interval, tissue PCNA mRNA abundance and protein levels were documented (by Northern and Western blot analysis, respectively) and compared with the results of PCNA immunostaining and 3H-thymidine incorporation into hepatic DNA. Tissue PCNA protein levels were also documented in additional groups of rats 12, 24, 36, and 48 hours after sham or 30% partial hepatectomy. PCNA mRNA expression after partial hepatectomy was variable: almost undetectable at 24 hours, levels returned to baseline at 36 hours, then fell again to low levels at 96 hours. PCNA protein levels remained stable for 36 hours, increased to fourfold above baseline (p < 0.01) at 48 hours, then remained elevated for the duration of the 96-hour study. Changes in PCNA by immunostaining were similar but tended to occur somewhat earlier (significant increases being detectable at 24 hours), whereas 3H-thymidine incorporation detected the earliest increases in DNA synthesis at 12 hours and peaked at 36 hours. Peak PCNA protein levels correlated with the extent (0%, 30%, or 70%) of hepatic resection. The results indicate that PCNA protein level as determined by Western blot analysis, but not PCNA mRNA expression, correlates with PCNA immunostaining and 3H-thymidine incorporation in the regenerating liver. These findings support the use of PCNA protein determinations as an additional quantitative measure of hepatic regenerative activity after partial hepatectomy in rats.
为了在大鼠模型中记录和比较增殖细胞核抗原(PCNA)mRNA和蛋白质水平与更传统的肝再生活性参数,成年雄性Sprague-Dawley大鼠(每组4至6只)在70%部分肝切除术后长达96小时的不同时间点处死。在每个时间间隔,记录组织PCNA mRNA丰度和蛋白质水平(分别通过Northern和Western印迹分析),并与PCNA免疫染色和3H-胸腺嘧啶核苷掺入肝DNA的结果进行比较。在假手术或30%部分肝切除术后12、24、36和48小时的另外几组大鼠中也记录了组织PCNA蛋白质水平。部分肝切除术后PCNA mRNA表达变化不定:24小时时几乎检测不到,36小时时水平恢复到基线,然后在96小时时再次降至低水平。PCNA蛋白质水平在36小时内保持稳定,48小时时增加至基线以上四倍(p<0.01),然后在96小时的研究期间一直保持升高。通过免疫染色检测到的PCNA变化相似,但往往发生得稍早一些(24小时时可检测到显著增加),而3H-胸腺嘧啶核苷掺入检测到DNA合成最早在12小时增加,并在36小时达到峰值。PCNA蛋白质水平峰值与肝切除范围(0%、30%或70%)相关。结果表明,通过Western印迹分析测定的PCNA蛋白质水平,而非PCNA mRNA表达,与再生肝中的PCNA免疫染色和3H-胸腺嘧啶核苷掺入相关。这些发现支持将PCNA蛋白质测定作为大鼠部分肝切除术后肝再生活性的额外定量指标。