Cytochemical localization of calcium and Ca2+,Mg2(+)-adenosine triphosphatase in colchicine-altered rat incisor ameloblastsDR Eisenmann, AH Salama, AM Zaki and SH Ashrafi Department of Histology, College of Dentistry, University of Illinois, Chicago. Colchicine is known to affect secretory, transport, and degradative functions of ameloblasts. The effects of colchicine on membrane- associated calcium and Ca2+,Mg2(+)-ATPase in secretory and maturation ameloblasts were investigated cytochemically. The pyroantimonate (PPA) method was used for localizing calcium and a modified Wachstein-Meisel medium was used to localize Ca2+,Mg2(+)-ATPase. Sections representing secretory and early maturation stages were examined by transmission electron microscopy. Morphological changes induced by colchicine included dislocated organelles and other well-established reactions to such anti-microtubule drugs. Calcium pyroantimonate (Ca-PA) deposits in most ameloblast types were markedly reduced, with the greater reduction occurring in those cells more severely altered morphologically. However, the cell membranes of both control and experimental smooth- ended maturation ameloblasts were essentially devoid of Ca-PA. The normal distribution and intensity of Ca2+,Mg2(+)-ATPase was not affected by colchicine. Because the observed reduction of membrane- associated calcium is apparently not mediated by Ca2+,Mg2(+)-ATPase in this case, other aspects of the calcium regulating system of ameloblasts are apparently targeted by colchicine.
Volume 38,
Issue 10,
pp. 1469-1478,
10/01/1990
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T. Kawamoto and M. Shimizu Pathway and Speed of Calcium Movement from Blood to Mineralizing Enamel J. Histochem. Cytochem., February 1, 1997; 45(2): 213 - 230. [Abstract] [Full Text] [PDF] |
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