克洛丹
紧密连接
血脑屏障
并行传输
封堵器
内皮干细胞
细胞生物学
势垒函数
癌细胞
癌症研究
生物
血管通透性
药物输送到大脑
癌症
磁导率
内分泌学
体外
中枢神经系统
生物化学
遗传学
膜
作者
Xinguo Zhuang,WENXIAO JI,Ziqian Fang,Yiming Yang,Fiona Ruge,QingPing Dou,Xun Li,BING XU,Wen G. Jiang,Tracey A. Martin
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2023-08-30
卷期号:43 (9): 3923-3934
被引量:1
标识
DOI:10.21873/anticanres.16580
摘要
Claudin-10 (CLDN10) is a membrane integral protein. It is one of the widely expressed tight junctional claudins with functions not well defined. In the present study, the expression profile and its role in cerebral endothelial cells and in the interaction between breast cancer and endothelial cells were investigated.CLDN10 expression was examined in a wide range of cell types. Brain endothelial cell models with or without CLDN10 expression were generated using the hCMEC/D3 cell line and used to test the barrier and permeability functions. Transendothelial drug delivery and invasion were also evaluated.hCMEC/D3 cells express high levels of CLDN10, compared with peripheral endothelial cells, mesothelial cells, fibroblasts, and breast cancer cells, which were either negative or expressed low levels of CLDN10. Knockdown of CLDN10 in hCMEC/D3 cells resulted in impaired tight junctions as seen by reduced transendothelial electric resistance and paracellular permeability. It also accelerated invasion of breast cancer cells through the endothelial cell layer. CLDN10 knockdown in hCMEC/D3 cells led to an increase in transendothelial chemodrug delivery. Furthermore, the SRC kinase inhibitor (AZM475271) was able to decrease the impedance and increase the paracellular permeability in cerebral endothelial cells.Cerebral endothelial cells express high levels of CLDN10, a protein regulating barrier function and thereby drug permeability and cancer invasiveness in brain endothelial cells, suggesting that it is a novel therapeutic target for the treatment of brain metastasis-related diseases.
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