Parsa I, Marsh W H, Sutton A L
Am J Pathol. 1980 Mar;98(3):649-62.
Organ-cultured embryonic rat pancreata were exposed to either single or multiple doses of methylnitrosourea (MNU), a single dose of MNU followed by 12-O-tetradecanoyl-phorbol-13-acetate (TPA), or TPA alone and cultured for up to 6 weeks. Both single and multiple doses of MNU caused similar alterations during the first 10 days; ie, for 4 days the explants grew and differentiated as untreated explants, forming acini and ductules; thereafter the presence of MNU induced ductular proliferation and hyperplasia. Explants exposed to a single dose of MNU failed to proliferate beyond the 10th day of culture, showed progressive cell necrosis, and became almost completely necrotic in 6 weeks. Cells prepared from these explants on Day 10 and injected subcutaneously into nude mice also failed to grow and degenerated after 2 weeks. Multiple doses of MNU in vitro, however, produced further proliferation with an atypical cribriform pattern by the 15th day. In the absence of MNU, treatment with TPA alone had no histologic effect; but TPA treatment after a single dose of MNU promoted abnormal growth similar to that produced by multiple doses of MNU. Cells prepared from 10-day explants treated with a single dose of MNU followed by TPA grew subcutaneously in nude mice and formed nodules of atypical growth within 2 weeks. This system constitutes a simple model of short-latency chemical carcinogenesis.
将器官培养的胚胎大鼠胰腺暴露于单剂量或多剂量的甲基亚硝基脲(MNU)、单剂量MNU后再给予12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)或仅给予TPA,并培养长达6周。单剂量和多剂量的MNU在最初10天引起相似的改变;即,在4天内,外植体像未处理的外植体一样生长和分化,形成腺泡和小导管;此后,MNU的存在诱导小导管增殖和增生。暴露于单剂量MNU的外植体在培养第10天后未能增殖,出现进行性细胞坏死,并在6周内几乎完全坏死。在第10天从这些外植体制备的细胞皮下注射到裸鼠体内,2周后也未能生长并发生退化。然而,体外给予多剂量的MNU在第15天时产生了具有非典型筛状模式的进一步增殖。在没有MNU的情况下,单独用TPA处理没有组织学效应;但单剂量MNU后给予TPA处理促进了与多剂量MNU产生的异常生长相似的生长。从用单剂量MNU接着TPA处理的10天龄外植体制备的细胞在裸鼠皮下生长,并在2周内形成非典型生长的结节。该系统构成了一个短期化学致癌作用的简单模型。