Endocytotic functions of ameloblasts and odontoblasts: Immunocytochemical and tracer studies on the uptake of plasma proteins

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Abstract
Background Biochemical, (immuno)cytochemical, and radioautographic data accumulated over several years have lead to the view that ameloblasts carry out both secretory and degradative functions throughout amelogenesis. Whereas it has been assumed that maturation stage ameloblasts endocytose aged enamel proteins from the enamel layer, the origin of the newly formed ones detected in the endosomal/lysosomal compartment of ameloblasts from all stages remains to be elucidated. One possible source is from secretory products released ectopically along basolateral surfaces. Methods To test this hypothesis, we have investigated, using colloidal gold immunocytochemistry, whether plasma proteins (albumin and α2HS‐glycoprotein) found in the interstitial fluid are endocytosed by rat incisor ameloblasts and other cells from hard and soft tissues. Rat albumin, tagged with dinitrophenol, was injected intravenously to trace the movement of this protein. Results Plasma proteins were immunodetected along the baso‐lateral surfaces and in multivesicular bodies of ameloblasts where enamel proteins were also found. By 2 hours following intravenous administration of dinitrophenylated albumin, the tracer had left the blood and diffused into the enamel organ and between odontoblasts and osteoblasts. The tracer was also found in multivesicular bodies of all cells examined. Conclusions The uptake of albumin by many different cell types suggests that this process is not restricted to ameloblasts and likely occurs in a nonselective manner. Hence, baso‐lateral uptake in ameloblasts may play a role not only in the continuous removal of plasma proteins leaking from the blood, but also of enamel proteins ‘dumped’ laterally between these cells. Likewise, odontoblasts may use the same mechanism to internalize some of the plasma proteins and any enamel protein that diffuse toward them.