Böcker W
Gerhard-Domagk-Institut für Pathologie, Universität Münster.
Verh Dtsch Ges Pathol. 2001;85:206-7.
In the present computer-assisted labelling study we demonstrate for the first time that in normal breast tissue keratin (K) 5+ progenitor cells give rise to either glandular (K 8/18+) or to myoepithelial cells (sm-actin = SMA+) via intermediary cells (either K 5/6+; K 8/18+ or K 5/6+; SMA+). Furthermore we have conclusive evidence that benign proliferative breast disease lesions are progenitor cell-derived lesions. In contrast, most breast cancers appear to evolve from glandularly differentiated cells. Western blotting experiments which show large amounts of K 5 in benign proliferative breast lesions, but not in ductal carcinoma in situ confirm the immunofluorescence data. Our results pave the way towards a new cell biological model of breast regeneration, benign proliferative breast disease and breast cancer.
在目前这项计算机辅助标记研究中,我们首次证明,在正常乳腺组织中,角蛋白(K)5+祖细胞通过中间细胞(K 5/6+;K 8/18+或K 5/6+;平滑肌肌动蛋白[SMA]+)产生腺上皮细胞(K 8/18+)或肌上皮细胞(平滑肌肌动蛋白[SMA]+)。此外,我们有确凿证据表明,乳腺良性增生性疾病病变是祖细胞来源的病变。相比之下,大多数乳腺癌似乎是由腺上皮分化细胞演变而来。蛋白质免疫印迹实验表明,乳腺良性增生性病变中有大量K 5,但原位导管癌中没有,这证实了免疫荧光数据。我们的结果为乳腺再生、乳腺良性增生性疾病和乳腺癌的新细胞生物学模型铺平了道路。