A freeze‐fracture study of the topographic relationship between inner enamel‐secretory ameloblasts in the rat incisor

A correlated study using freeze‐fracture replicas and routine thin sectioning was done on the ameloblasts which secrete inner enamel in the rat incisor. These ameloblasts are columnar cells aligned in rows parallel to the cross‐sectional plane of the incisor. Each cell has a Tomes' process at its distal end which is contained within a cavity of interrod enamel. Tomes' processes of a particular row of cells are inclined towards the mesial side of the tooth, while those of the next row are inclined towards the lateral side, so that the processes cross each other at 90°. Freeze‐fracture replicas were used to examine the surfaces of ameloblasts between adjacent rows and the surfaces of the cells within the row. Replicas of the surfaces between rows showed that ameloblasts are curved so that their proximal and distal ends (Tomes' processes) are both directed towards the same side of the tooth. The surface of each row bears the impression left upon it by the cells in the adjacent row which have been fractured away. This cell‐impression is also curved, but in the opposite direction to the cells which it crosses. It was thus shown that not only the Tomes' processes of adjacent rows but the entire cell bodies cross one another. This crossing is slight at the proximal ends of the cells, but marked at the level of the distal junctional complex. At this level a cell from a particular row curves across several cells of the neighbouring row and forms large tight junctions with at least two cells in that row. The proximal and distal junctional complexes form zones of tight junctions around the cell. The distal complex is more extensive than the proximal and the tight junctions are better developed between adjacent rows. Gap junctions are, however, larger between cells within the rows. The study demonstrated the effectiveness of freeze‐fracture replicas in obtaining 3‐dimensional details about ameloblast shape, and this information was used to evaluate the supposed movement of ameloblasts during inner enamel formation.