Tsuji S, Ogawa K, Takasaka H, Sonoda T, Mori M
Department of Pathology, Sapporo Medical College.
Jpn J Cancer Res. 1988 Feb;79(2):148-51. doi: 10.1111/j.1349-7006.1988.tb01569.x.
Since the deficiency of ornithine carbamoyltransferase (OCT) is inherited as an X-linked dominant trait in sparse-fur with abnormal skin and hair (Spf-ash) mice, the livers of heterozygous Spf-ash females show mosaicism in regard to OCT. We induced enzyme-altered foci and nodules, presumptive preneoplastic lesions for hepatocellular carcinomas, in the livers of OCT mosaic mice (Spf-ash x C3H F1), and investigated the clonality of the lesions. Simultaneous histochemical staining for OCT and gamma-glutamyl transpeptidase (GGT) demonstrated that all GGT-positive lesions (ranging in size from 3 cells to a few millimeters in diameter) were either positive or negative for OCT, and no mosaic lesions were detectable. The results indicate that individual enzyme-altered hepatocytic lesions are the result of clonal proliferation.
由于鸟氨酸氨甲酰基转移酶(OCT)缺乏症在稀疏毛发伴皮肤和毛发异常(Spf-ash)小鼠中作为X连锁显性性状遗传,杂合子Spf-ash雌性小鼠的肝脏在OCT方面表现出镶嵌性。我们在OCT镶嵌小鼠(Spf-ash×C3H F1)的肝脏中诱导了酶改变灶和结节,即肝细胞癌的推定癌前病变,并研究了这些病变的克隆性。对OCT和γ-谷氨酰转肽酶(GGT)进行同步组织化学染色显示,所有GGT阳性病变(大小从3个细胞到直径几毫米不等)对OCT要么呈阳性,要么呈阴性,未检测到镶嵌病变。结果表明,单个酶改变的肝细胞病变是克隆增殖的结果。