Pregled bibliografske jedinice broj: 399172
Modified embryo organ culture model system for preclinical studies of growth factor-induced neural tissue differentiation in mammals
Modified embryo organ culture model system for preclinical studies of growth factor-induced neural tissue differentiation in mammals // 9th International Conference on Alzheimer's and Parkinson's diseases
Prag, Češka Republika, 2009. str. 223-223 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 399172 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Modified embryo organ culture model system for preclinical studies of growth factor-induced neural tissue differentiation in mammals
Autori
Stipić, Jagoda ; Crbek-Kunstelj, Vesna
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
9th International Conference on Alzheimer's and Parkinson's diseases
/ - , 2009, 223-223
Skup
9th International Conference on Alzheimer's and Parkinson's diseases
Mjesto i datum
Prag, Češka Republika, 11.03.2009. - 15.03.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
embryo culture; growth factor; differentiation
Sažetak
Aims: Fibroblast growth factor (FGF) and nerve growth factor (NGF) are found in various parts of human and vertebrate embryos during development. The development of the vertebrate nervous system begins with the inductive differentiation of the neural plate from the dorsal side of flat ectoderm at the end of gastrulation. The role of FGF and NGF in critical period for mammalian development, gastrulation, was studied. Material and methods: In our laboratory a unique organ culture system of mammalian embryo was designed. Embryonic parts of the whole gastrulating rat embryos were cultivated on the stainless-steel grid supported lens paper, at the air-liquid interface during two weeks using liquid serum-free and protein-free medium. A signal-protein FGF or NGF (100 ng/ml and 200 ng/ml) were added, or both together in culture medium in time frame of 2, 5 or 9 days. Results: Embryos developed into teratoma built of intermixed tissues, including nerve tissue. In control serum-free medium neuroblasts were absent. NGF did never improve differentiation of neuroblasts. FGF significantly stimulated the differentiation of neural tissue during 5 days, and the best during 9 days. In FGF/NGF-treated embryos differentiation of neuroblasts was the same as was in FGF-treated. Conclusions: Our model system is simpler than the embryo in vivo, but closer to normal development than the cell cultures used in other studies. The neuroblasts found were direct answer to molecular signals added. This fact is in accordance with the idea that in a multi-level process of neural differentiation, FGF is the neural inducer in mammals.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1080399-0335 - Eksperimentalni embrionalni tumori i razvoj zametaka sisavaca in vitro i in vivo (Jakuš, Florijana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb