Pregled bibliografske jedinice broj: 134155
Differentiation of mouse egg-cylinders cultured in vitro
Differentiation of mouse egg-cylinders cultured in vitro // Proceedings 6th Multinational Congress on Microscopy-European Extension- / Milat, Ognjen ; Ježek, Davor (ur.).
Zagreb: Hrvatsko mikroskopijsko društvo, 2003. str. 347-8 (poster, međunarodna recenzija, cjeloviti rad (in extenso), znanstveni)
CROSBI ID: 134155 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Differentiation of mouse egg-cylinders cultured in vitro
Autori
Stević, Nataša ; Belovari, Tatjana ; Kostović-Knežević, Ljiljana
Vrsta, podvrsta i kategorija rada
Radovi u zbornicima skupova, cjeloviti rad (in extenso), znanstveni
Izvornik
Proceedings 6th Multinational Congress on Microscopy-European Extension-
/ Milat, Ognjen ; Ježek, Davor - Zagreb : Hrvatsko mikroskopijsko društvo, 2003, 347-8
Skup
6th Multinational Congress on Microscopy-European Extension-
Mjesto i datum
Pula, Hrvatska, 01.06.2003. - 05.06.2003
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
mouse embryo; culture in vitro; differentiation
Sažetak
Mammalian embryo culture systems are used for studying normal and abnormal embryo development1, 2. In present study postimplantation mouse embryos without extraembryonic parts were cultivated in vitro to determine sequence of appearance of various tissues and the time needed for their differentiation. Embryonic development in vitro was compared with development in vivo. Gastrulating CD1 mouse embryos E7.5 were cultivated in Dulbecco's Modified Eagle Medium with 20% foetal bovine serum. After 1, 2, 3, 4, 7, and 14 days explants were taken for histology and serial semithin sections were prepared and analysed by light microscopy. After 3 days of culture neural (Fig 1.) and surface epithelium, and columnar epithelium corresponding to the primitive gut was present in the explants. From fourth till seventh day the neuroepithelium with noticeable basal lamina formed small cysts in the mesenchyme. After 14 days of culture more differentiated derivatives of all three germ layers were present. Among others, stratified squamous epithelium, cartilage with perichondrium and pseudostratified columnar epithelium with ciliae and goblet cells were observed. The present findings indicate that after cultivation of gastrulating mouse embryos, structures like neuroepithelium and primitive gut were observed two days later than in vivo. Although we used significantly lower percentage of serum than in previous studies, after two-weeks of culture all main tissue types were present.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA