克洛丹
转染
内化
细胞生物学
并行传输
HEK 293细胞
化学
紧密连接
磷酸化
细胞内
细胞
膜
生物
生物化学
受体
基因
磁导率
作者
Jan Rossa,Dorothea Lorenz,Martina Ringling,Anna Veshnyakova,Jörg Piontek
标识
DOI:10.1111/j.1749-6632.2012.06546.x
摘要
Tight junctions (TJs) regulate paracellular barriers and claudins (Cld) form the backbone of TJ strands. To elucidate the molecular mechanism of claudin polymer formation, TJs were reconstituted by claudin transfection of TJ‐free HEK293 cells. Therewith, typical TJ stands can be found at cell–cell contacts. In addition, overexpression of Cld5‐YFP induces formation of huge intracellular multilamellar bodies. In contrast, Cld3 does not induce similar structures. Inhibition of trans ‐interaction of Cld5 by Y148A substitution diminished formation of multilamellar bodies. These results demonstrate claudin subtype‐specific oligomerization. Cld3 and Cld5 localize to the plasma membrane differentially. Phosphorylation at T207 of Cld5 was suggested to participate in regulation of Cld5 internalization. However, prevention of potential phosphorylation by T207A substitution did not increase Cld5 amount in the plasma membrane of transfected cells. Taken together, if carefully evaluated, transfection of claudin constructs in nonpolar cells is a powerful strategy to improve understanding of subcellular targeting and assembly of TJ proteins.
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