Parsons D F, Marko M, Wansor K J
Tissue Cell. 1983;15(4):499-507. doi: 10.1016/0040-8166(83)90001-0.
A carcinoma invasion system (Krebs-2 and Ehrlich tetraploid ascites tumors invading mouse peritoneum) was studied by high-voltage electron microscope (HVEM) stereoscopy, conventional (medium voltage) electron microscopy (MVEM), and cytochemistry. Tumor cells entered areas of peritoneum (mainly parietal) only where mesothelial cells were damaged and where there was inflammation of the underlying stroma. The initial invasion was different from that of most other invading carcinomas in that there was minimal breakdown of basal lamina and collagen. Neither tumor cells, inflammatory leukocytes nor peritoneal fibroblasts showed significant secondary lysosome production or release of intracellular or extracellular acid phosphatase. Morphological and cytochemical criteria suggest that in some invading carcinomas, as with non-tumor migrating cells such as leukocytes, widespread proteolysis due to diffusion of proteases is not a prerequisite for invasion of stromal connective tissue.
利用高压电子显微镜(HVEM)立体显微镜技术、传统(中压)电子显微镜(MVEM)以及细胞化学方法,对一种癌侵袭系统(克雷布斯-2和艾氏四倍体腹水瘤侵袭小鼠腹膜)进行了研究。肿瘤细胞仅进入间皮细胞受损且其下方基质存在炎症的腹膜区域(主要是壁腹膜)。初始侵袭与大多数其他侵袭性癌不同,在于基底膜和胶原的破坏极少。肿瘤细胞、炎性白细胞及腹膜成纤维细胞均未显示出明显的继发性溶酶体产生或细胞内及细胞外酸性磷酸酶的释放。形态学和细胞化学标准表明,在一些侵袭性癌中,如同白细胞等非肿瘤迁移细胞一样,蛋白酶扩散导致的广泛蛋白水解并非侵袭基质结缔组织的必要条件。