Smith G J, Lykke A W
J Pathol. 1985 Nov;147(3):165-72. doi: 10.1002/path.1711470304.
The epithelial cell strain NAL1A cultured from normal adult mouse lung has been transformed by culturing in dexamethasone into an invasive neoplastic cell strain. The criteria for neoplastic transformation include the capacity for anchorage independent growth in soft agar as well as the formation of invasive neoplastic nodules after subcutaneous transplantation in thymectomized irradiated newborn mice. The cells of the invasive neoplastic nodules induced by dexamethasone culturing of NAL1A were indistinguishable histopathologically and by electron microscopy from invasive nodules evoked by the subcutaneous inoculation of CMT64, a cell line cultured from a metastasizing mouse lung tumour and cell strain NUL1 derived from mouse pulmonary adenomata induced by urethane. Cells of the nodules derived from all three cultured strains possessed desmosomes, surface microvilli and phospholipid lamellar bodies characteristic of the type 2 pneumocyte. It is concluded that cultured cell strains NAL1A, cultured in dexamethasone, NUL1 and CMT64 evoke invasive subcutaneous neoplasms derived from a common ancestor, presumably a type 2 pneumocyte related stem cell.
从正常成年小鼠肺中培养出的上皮细胞系NAL1A,通过在 Dexamethasone 中培养已转化为侵袭性肿瘤细胞系。肿瘤转化的标准包括在软琼脂中进行非贴壁依赖性生长的能力,以及在胸腺切除并经照射的新生小鼠皮下移植后形成侵袭性肿瘤结节的能力。经 Dexamethasone 培养诱导的 NAL1A 侵袭性肿瘤结节的细胞,在组织病理学和电子显微镜下与通过皮下接种 CMT64(一种从转移性小鼠肺肿瘤培养出的细胞系)以及由氨基甲酸乙酯诱导的小鼠肺腺瘤衍生的细胞系 NUL1 所诱发的侵袭性结节无法区分。源自所有三种培养系的结节细胞都具有桥粒、表面微绒毛和Ⅱ型肺细胞特有的磷脂板层小体。结论是,经 Dexamethasone 培养的细胞系 NAL1A、NUL1 和 CMT64 诱发的侵袭性皮下肿瘤源自一个共同祖先,大概是一种与Ⅱ型肺细胞相关的干细胞。