Possible involvement of phosphorylation of occludin in tight junction formation

Abstract

Occludin is an integral membrane protein localizing at tight junctions in epithelial and endothelial cells. Occludin from confluent culture MDCK I cells resolved as several (> 10) bands between 62 and 82 kD in SDS-PAGE, of which two or three bands of the lowest M(r) were predominant. Among these bands, the lower predominant bands were essentially extracted with 1% NP-40, whereas the other higher M(r) bands were selectively recovered in the NP-40- insoluble fraction. Alkaline phosphatase treatment converged these bands of occludin both in NP-40-soluble and -insoluble fractions into the lowest M(r) band, and phosphoamino acid analyses identified phosphoserine (and phosphothreonine weakly) in the higher M(r) bands of occludin. These findings indicated that phosphorylation causes an upward shift of occludin bands and that highly phosphorylated occludin resists NP-40 extraction. When cells were grown in low Ca medium, almost all occludin was NP-40 soluble. Switching from low to normal Ca medium increased the amount of NP-40-insoluble occludin within 10 min, followed by gradual upward shift of bands. This insolubilization and the band shift correlated temporally with tight junction formation detected by immunofluorescence microscopy. Furthermore, we found that the anti-chicken occludin mAb, Oc-3, did not recognize the predominant lower M(r) bands of occludin (non- or less phosphorylated form) but was specific to the higher M(r) bands (phosphorylated form) on immunoblotting. Immunofluorescence microscopy revealed that this mAb mainly stained the tight junction proper of intestinal epithelial cells, whereas other anti-occludin mAbs, which can recognize the predominant lower M(r) bands, labeled their basolateral membranes (and the cytoplasm) as well as tight junctions. Therefore, we conclude that non- or less phosphorylated occludin is distributed on the basolateral membranes and that highly phosphorylated occludin is selectively concentrated at tight junctions as the NP-40 insoluble form. These findings suggest that the phosphorylation of occludin is a key step in tight junction assembly.