2002
Proliferating Cell Nuclear Antigen (PCNA) Expression in Tooth Primordia in the Field Vole (Microtus agrestis, Rodentia)
MATULOVÁ, Petra, Kirsti WITTER a Ivan MÍŠEKZákladní údaje
Originální název
Proliferating Cell Nuclear Antigen (PCNA) Expression in Tooth Primordia in the Field Vole (Microtus agrestis, Rodentia)
Název česky
Exprese PCNA v zubních základech hraboše mokřadního (Microtus agrestis, Rodentia)
Autoři
MATULOVÁ, Petra (203 Česká republika, garant), Kirsti WITTER (276 Německo) a Ivan MÍŠEK (203 Česká republika)
Vydání
(Microtus agrestis, Rodentia), Taylor and Francis, 2002, 0300-8207
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Francie
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.646
Organizační jednotka
Přírodovědecká fakulta
Klíčová slova anglicky
Dentition; Odontogenesis; Proliferation Marker; Embryo; Development
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 18. 11. 2008 14:07, RNDr. Petra Matulová, CSc.
V originále
Cell proliferation in developing tooth germs has been studied particularly using bromodeoxyuridine (BrdU) incorporation into growing tooth primordia and by counting and three-dimensional (3D) reconstruction of mitoses in serial sections of developing teeth. PCNA has been proposed as an alternative marker of proliferation activity. The aim of our study was to detect immunohistochemically locations of PCNA-positive cells in developing tooth germs of Microtus agrestis (Rodentia). PCNA expression could be distinguished in oral epithelium and mesenchyme before first signs of dental lamina elevation. During bud, cap, and bell stages, positive immunostaining could be observed at defined sites in enamel organ, tooth papilla, and dental follicle. Rudimental tooth germs of the upper diastema, enamel knots, and inner enamel epithelium at day of ontogeny 18 and 19 showed negative reaction. PCNAmarks cycling and early G0 cells and can be used successfully as a proliferation marker even in collection material.
Česky
Cell proliferation in developing tooth germs has been studied particularly using bromodeoxyuridine (BrdU) incorporation into growing tooth primordia and by counting and three-dimensional (3D) reconstruction of mitoses in serial sections of developing teeth. PCNA has been proposed as an alternative marker of proliferation activity. The aim of our study was to detect immunohistochemically locations of PCNA-positive cells in developing tooth germs of Microtus agrestis (Rodentia). PCNA expression could be distinguished in oral epithelium and mesenchyme before first signs of dental lamina elevation. During bud, cap, and bell stages, positive immunostaining could be observed at defined sites in enamel organ, tooth papilla, and dental follicle. Rudimental tooth germs of the upper diastema, enamel knots, and inner enamel epithelium at day of ontogeny 18 and 19 showed negative reaction. PCNAmarks cycling and early G0 cells and can be used successfully as a proliferation marker even in collection material.