Knuechel R, Burgau M, Rueschoff J, Hofstaedter F
Institute of Pathology, University of Regensburg, Germany.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(3):137-44. doi: 10.1007/BF02915106.
To evaluate proliferating cell nuclear antigen (PCNA) staining for assessing proliferative activity in routine pathology specimens of urinary bladder, the bladder carcinoma cell line J82 and a total of 122 specimens of normal bladder and urothelial lesions were stained with the antibody clone PC10 against proliferating cell nuclear antigen. In in vitro plateau cultures the proportion of PCNA-positive cells exceeded that of Ki-67-positive cells, and only very few cells were negative. In formalin-fixed tissues, the PCNA staining pattern, which should be confined to replicon units in the nucleus, was optimized by 1 h postfixation in an organic solvent (methacarn). Sections showed positive nuclear staining confined to basal and some suprabasal cells in normal urothelium and grade 1 dysplasias, but more generalized nuclear staining in all other neoplastic lesions. In addition, stromal cells adjacent to invasive tumors showed nuclear positivity in some instances. Using quantitative true color image analysis of sections counterstained with hemalum, the degree of brown staining of the PCNA reaction product is contrasted with the blue staining of the nuclear area. With this method low contrast specific staining not appreciated optically can be reliably detected. Image analysis data confirmed observations made on noncounterstained sections and showed significant differences between grade 1 and 2 dysplasias as well as between grade 1 dysplasia and all grades of papillary tumor. Furthermore, a significant difference in PCNA staining indices was found between grade 1 and 3 bladder carcinomas. The results indicate that PCNA staining using the PC10 antibody is not confined to the proliferative fraction of neoplastic urothelium.(ABSTRACT TRUNCATED AT 250 WORDS)
为评估增殖细胞核抗原(PCNA)染色在膀胱常规病理标本中评估增殖活性的作用,用抗增殖细胞核抗原的抗体克隆PC10对膀胱癌细胞系J82以及总共122例正常膀胱和尿路上皮病变标本进行染色。在体外平台培养中,PCNA阳性细胞的比例超过Ki-67阳性细胞,只有极少数细胞呈阴性。在福尔马林固定组织中,PCNA染色模式应局限于细胞核中的复制子单位,通过在有机溶剂(甲醇-冰醋酸固定液)中固定1小时进行优化。切片显示正常尿路上皮和1级发育异常中阳性核染色局限于基底细胞和一些基底上层细胞,但在所有其他肿瘤性病变中核染色更广泛。此外,侵袭性肿瘤附近的基质细胞在某些情况下显示核阳性。使用苏木精复染切片的定量真彩色图像分析,将PCNA反应产物的棕色染色程度与核区域的蓝色染色进行对比。通过这种方法,可以可靠地检测到光学上不易察觉的低对比度特异性染色。图像分析数据证实了在未复染切片上的观察结果,并显示1级和2级发育异常之间以及1级发育异常与所有级别的乳头状肿瘤之间存在显著差异。此外,在1级和3级膀胱癌之间发现PCNA染色指数存在显著差异。结果表明,使用PC10抗体的PCNA染色不限于肿瘤性尿路上皮的增殖部分。(摘要截断于250字)