Wu Qiong, Liu Ya-fang, Ren Yue, Xu Xiao-ming, Yu Li-na, Li Yu-lin, Quan Cheng-shi
Key laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Zhonghua Yi Xue Za Zhi. 2010 Feb 9;90(6):407-12.
To explore the effect of over-expression of tight junction protein claudin-6 upon the biological characters of breast cancer cell line MCF-7.
The MCF-7 subline expressing a high level of claudin-6 was established by transfection with a pcDNA3.1-claudin-6 expression vector. The expression of claudin-6 in mRNA and its protein level were confirmed by RT-PCR, Western blot and immunofluorescent assays. Then the effect of claudin-6 upon cell proliferation was examined by MTT assay. Colony-forming assays were used to examine 2-D and 3-D colony-forming capacities. Invasive and migratory traits of claudin-6 expressing cells were determined by Boyden chamber invasion assay and monolayer wound-healing assay. The structure and function of tight junctions in both parental and claudin-6 expression MCF-7 cells were evaluated by measuring transepithelial electrical resistance.
Immunofluorescent assays showed that transfected cells expressed claudin-6 on their membrane. Cells with a high level expression of claudin-6 grew slowly than control cells. Anchorage-independent growth, invasive and migratory traits also decreased substantially in cells with claudin-6 expression; whereas the transepithelial electrical resistance increased in the claudin-6 transfected cells.
The up-regulation of claudin-6 expression in MCF-7 breast cancer cells suppresses their malignant phenotypes with a correlation with the restoration of tight junction integrity. Claudin-6 may function as a cancer suppressor whose down-regulation contributes to the malignant progression of certain types of breast cancers.
探讨紧密连接蛋白claudin-6过表达对乳腺癌细胞系MCF-7生物学特性的影响。
通过用pcDNA3.1-claudin-6表达载体转染建立高表达claudin-6的MCF-7亚系。通过RT-PCR、蛋白质印迹法和免疫荧光测定法确认claudin-6在mRNA和蛋白质水平的表达。然后通过MTT法检测claudin-6对细胞增殖的影响。采用集落形成试验检测二维和三维集落形成能力。通过Boyden小室侵袭试验和单层划痕愈合试验测定表达claudin-6的细胞的侵袭和迁移特性。通过测量跨上皮电阻评估亲本MCF-7细胞和表达claudin-6的MCF-7细胞中紧密连接的结构和功能。
免疫荧光测定显示转染细胞在其膜上表达claudin-6。claudin-6高表达的细胞比对照细胞生长缓慢。在表达claudin-6的细胞中,非锚定依赖性生长、侵袭和迁移特性也显著降低;而在转染claudin-6的细胞中跨上皮电阻增加。
MCF-7乳腺癌细胞中claudin-6表达上调抑制其恶性表型,这与紧密连接完整性的恢复相关。claudin-6可能作为一种肿瘤抑制因子,其下调促成某些类型乳腺癌的恶性进展。