Rehm S, Ward J M
Tumor Pathology and Pathogenesis Section, National Cancer Institute, Frederick, Maryland 21701.
Toxicol Pathol. 1989;17(4 Pt 2):737-42. doi: 10.1177/0192623389017004201.
Alveolar type II cell tumors were induced transplacentally by intraperitoneal injection of pregnant C3H/HeNCr MTV- or Swiss Webster mice with N-nitrosoethylurea at a dose of 0.5 mmol/kg and 0.74 mmol/kg. At different time points after birth (1-32 weeks), the entire lungs from 40 of the male offspring were inflated with Bouin's fixative, separated into lobes, and sectioned at 5 microns serially to detect every microscopic lesion. Results were compared with those obtained from examining only every 10th, 20th, or a single midlevel section from the same material. On average, 150 serial sections were prepared per mouse lung. Initially, only purely solid/alveolar or purely tubulopapillary types were observed but with tumor progression, papillary structures developed within solid tumors resulting in mixed neoplasms. Analyzing mouse lungs in step sections of every 10th section (50-60 microns), 5/238 (2%) of the tumors were missed, in step sections of every 20th section (100-120 microns), 16/238 (7%) of the tumors were not detected and usually less than half of the tumors were seen in the single mid-level section. The approximate size of the neoplasms is indicated by the total number of sections per tumor. The dimensions of tumors evaluated with step sections of 10 or 20 were comparable to the size observed with serial sections. It is concluded that the evaluation of mouse lung tumors in steps of approximately 50 microns is basically equivalent to the study of serial sections and appears to be a feasible method to assess the complete incidence, histological type, and size of all proliferative processes throughout the entire lung.
通过给怀孕的C3H/HeNCr MTV小鼠或瑞士韦伯斯特小鼠腹腔注射剂量为0.5 mmol/kg和0.74 mmol/kg的N-亚硝基乙基脲,经胎盘诱导产生肺泡II型细胞瘤。在出生后的不同时间点(1 - 32周),将40只雄性后代的整个肺用Bouin固定液充气,分成肺叶,并连续切成5微米厚的切片以检测每个微观病变。将结果与仅检查同一材料的每第10个、第20个或单个中层切片所获得的结果进行比较。平均每只小鼠肺制备150个连续切片。最初,仅观察到纯实性/肺泡型或纯管状乳头状型,但随着肿瘤进展,实性肿瘤内出现乳头状结构,导致混合性肿瘤。分析每第10个切片(50 - 60微米)的步进切片中的小鼠肺,5/238(2%)的肿瘤被漏检,在每第20个切片(100 - 120微米)的步进切片中,16/238(7%)的肿瘤未被检测到,并且在单个中层切片中通常只能看到不到一半的肿瘤。肿瘤的大致大小由每个肿瘤的切片总数表示。用10或20步切片评估的肿瘤尺寸与连续切片观察到的大小相当。结论是,以大约50微米的步长评估小鼠肺肿瘤基本上等同于连续切片研究,并且似乎是一种可行的方法,可用于评估整个肺中所有增殖过程的完整发病率、组织学类型和大小。