Pregled bibliografske jedinice broj: 709217
Expression of pluripotency markers during mesenchymal stem cell differentiation
Expression of pluripotency markers during mesenchymal stem cell differentiation // EU FP7 Project Glowbrain Workshop “Stem Cell Techniques”
Zagreb: Croatian Institute for Brain Research, 2013. (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 709217 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Expression of pluripotency markers during mesenchymal stem cell differentiation
Autori
Matic, Igor ; Antunovic, Maja ; Kriznik, Bojana ; Brkic, Sime ; Josipovic, Pavle ; Ivkovic, Alan ; Caput Mihalic, Katarina ; Pecina, Marko ; Karlak, Ivan ; Marijanovic, Inga.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
EU FP7 Project Glowbrain Workshop “Stem Cell Techniques”
/ - Zagreb : Croatian Institute for Brain Research, 2013
Skup
EU FP7 Project Glowbrain Workshop “Stem Cell Techniques”
Mjesto i datum
Zagreb, Hrvatska, 23.05.2013
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Mesenchymal stem cells; Oct4; Sox2; Nanog
Sažetak
The purpose of this study was to determine the levels of expression of pluripotency genes Oct4, Sox2 and Nanog during the osteogenic differentiation of multipotent mesenchymal stem cells. Mesenchymal stem cells were derived from the human bone marrow and differentiated into osteoblasts. The analyses were performed on days 0 and 14 of the cell culture. In vitro differentiation was evaluated by the analysis of bone markers – alkaline phosphatase activity and the mRNA expression of dentin matrix protein 1 (DMP1) and bone sialoprotein (BSP). The Oct4, Sox2 and Nanog expression was evaluated at mRNA level by real-time qPCR and at protein level by immunocytochemistry. Results: In vitro cultures on day 14 showed an increase in alkaline phosphatase activity as well as the upregulation of DMP1 and BSP. Analysis of Oct4, Sox2 and Nanog transcripts in undifferentiated hMSC on day 0 showed that their expression decreases together with the appearance and increase of bone markers. However, immunocytochemistry detected only Oct4 transcription factor and it was localized in cell nuclei, prior (day 0) and post differentiation (day 14). On the same time points, cultures were negative for SOX2 and NANOG proteins. Conclusion: From presented data we conclude that pluripotency markers Oct4, Sox2 and Nanog are present in mesenchymal stem cells at mRNA level and that their transcription is decreasing as the differentiation proceeds. However, mRNA levels do not reflect the protein levels suggesting the posttranscriptional regulation of protein expression.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Alan Ivković
(autor)
Igor Matić
(autor)
Marko Pećina
(autor)
Inga Urlić
(autor)
Katarina Caput Mihalić
(autor)