Effects of Feeder Cell Types on Culture of Mouse Embryonic Stem Cell In Vitro

• Published in: Balsaeng'gwa saengsig Vol. 19; no. 3; pp. 119 - 126
• Main Authors: Park, Yun-Gwi, Lee, Seung-Eun, Kim, Eun-Young, Hyun, Hyuk, Shin, Min-Young, Son, Yeo-Jin, Kim, Su-Young, Park, Se-Pill
• Format: Journal Article
• Language: Korean
• Published: 2015
• Subjects: Feeder cell; Mouse embryonic stem cell; MEF feeder cell; Pluripotency marker
• ISSN: 2465-9525; 2465-9541

The suitable feeder cell layer is important for culture of embryonic stem (ES) cells. In this study, we investigated the effect of two kinds of the feeder cell, MEF cells and STO cells, layer to mouse ES (mES) cell culture for maintenance of stemness. We compare the colony formations, alkaline phosphatase (AP) activities, expression of pluripotency marker genes and proteins of D3 cell colonies cultured on MEF feeder cell layer (D3/MEF) or STO cell layers (D3/STO) compared to feeder free condition (D3/-) as a control group. Although there were no differences to colony formations and AP activities, interestingly, the transcripts level of pluripotency marker genes, Pou5f1 and Nanog were highly expressed in D3/MEF (79 and 93) than D3/STO (61and 77) or D3/- (65 and 81). Also, pluripotency marker proteins, NANOG and SOX-2, were more synthesized in D3/MEF ($72.8{\pm}7.69$ and $81.2{\pm}3.56$) than D3/STO ($32.0{\pm}4.30$ and $56.0{\pm}4.90$) or D3/- ($55.0{\pm}4.64$ and $62.0{\pm}6.20$). These results suggest that MEF feeder cell layer is more suitable to mES cell culture.