ƒAƒNƒeƒBƒuƒ{[ƒhE‚TŒŽ

ŒF–{‘åŠwEˆâ“`ŽqŽÀŒ±Ž{Ý
ŒF–{Žs–{‘‘‚Q|‚Q|‚P
Tel : (096) 373-6501, FAX : (096)373-6502
‚Q‚O‚O‚Q”N@‚TŒŽ@‚U“ú@XV


ƒAƒNƒeƒBƒuƒ{[ƒhE‚Q‚O‚O‚Q”N@‚TŒŽ

Œ¤‹†”­•\‚ðs‚Á‚½Šw‰ïG‘æ‚Q‚S‰ñ“ú–{•ªŽq¶•¨Šw‰ï”N‰ï
‚Q‚O‚O‚P”N‚P‚QŒŽ‚X“ú`‚P‚Q“úi‰¡•lj
ƒ^ƒCƒgƒ‹GInvolvement of Oct-3/4 in SDIA-mediated neurogenesis of ES cells
”­•\ŽÒG‰ºè@NŽ¡@Ž
@@@i”­¶ˆãŠwŒ¤‹†ƒZƒ“ƒ^[@“]ŽÊ§Œä•ª–ìj
AbstractG
Oct-3/4, which belongs to the POU transcription factor superfamily, plays a critical role in maintaining pluripotency of embryonic stem cells. It has been recently reported that neurogenesis of ES cells is dramatically promoted by SDIA (for stromal cell-derived inducing activity), which accumulates on the surface of a stromal cell line PA6. We here demonstrate that Oct-3/4, a master regulator of ES cell pluripotency, also plays a critical role in the process of SDIA-mediated neurogenesis of ES cells. The expression of Oct-3/4 was found to be sustained in ES cells cultured with SDIA but downregulated when SDIA was omitted. Furthermore, when Oct-3/4 was continuously expressed in ES cells using a tetracycline-regulated expression system, efficient neuronal differentiation in serum-free conditions was observed even in the absence of SDIA. The continuous expression of Oct-3/4 accelerated the differentiation of ES cells to primitive ectoderm and promoted the appearance of cells positive for Nestin, a neural stem/precursor cell marker. Moreover, SDIA-mediated neurogenesis of ES cells was enhanced by the continuous Oct-3/4 expression. Taken together, it is conceivable that Oct-3/4 functions as a key regulator in the primitive neural stem cell formation and the SDIA-mediated neurogenesis of ES cells.


@@ƒAƒNƒeƒBƒuƒ{[ƒh
ŒF–{‘åŠwEˆâ“`ŽqŽÀŒ±Ž{Ý; E-mail:www@gtc.gtca.kumamoto-u.ac.jp