The tight junction does not allow lipid molecules to diffuse from one epithelial cell to the next

The tight junction (zonula occludens) links epithelial cells into a monolayer by forming a continuous belt of sealing contacts around the apex of each cell. They appear in thin sections as if they were 'fusions' between the apposed plasma membranes and in freeze-fracture replicas as patterns of complementary strands and furrows. These images have led to the proposal that the core of the tight junction is formed by a hexagonal cylinder of lipids. In this model, the cytoplasmic leaflet of the apical and basolateral plamsa membrane domains would be continuous, whereas the exoplasmic leaflets of the two plasma membrane domains of the same cell would be separated at the tight junction and are instead predicted to be continuous between the plasma membranes of neighbouring cells. We demonstrate here that this prediction does not hold true. An endogenous glycoliped (Forssman antigen), present in the exoplasmic leaflet of the apical membrane of MDCK strain II cells, is unable to pass to MDCK strain I cells (which lack this glycolipid) under conditions where these cells are connected by tight junctions. In addition, fluorescent lipids which have been fused into the plasma membrane of one MDCK cell do not diffuse to neighbouring cells while the tight junctions between the cells are intact

N-glycans as apical sorting signals in epithelial cells

In epithelial Madin-Darby canine kidney (MDCK) cells newly synthesized molecules are sorted in the trans-Golgi network and directly delivered to their apical and basolateral surface destinations. Sorting is mediated by signals in the cytoplasmic domains of basolateral transmembrane proteins whereas glycosylphosphatidylinositol-linked proteins have apical sorting information in their glycolipid tails. Signals for apical transmembrane proteins are thought to reside in their ectodomains, because truncated forms lacking the cytoplasmic tail and the membrane anchor are secreted apically. Here we demonstrate that carbohydrates act as an apical targeting signal for secretory proteins. Growth hormone, which is non-glycosylated and secreted from both sides of MDCK cell layers, is secreted from the apical side when glycosylated. Thus glycans not only play a general role in protein folding but also appear to function in protein sorting in biosynthetic traffic