生物
P19电池
细胞生物学
同源盒蛋白纳米
细胞效价
SOX2
细胞分化
胚胎干细胞
染色质
雷克斯1
诱导多能干细胞
细胞命运测定
转录因子
遗传学
基因
作者
Julie Massé,Claire Piquet‐Pellorce,Justine Viet,Daniel Guerrier,Isabelle Pellerin,Stéphane Deschamps
标识
DOI:10.1016/j.yexcr.2011.04.015
摘要
The nuclear zinc finger protein ZFPIP/Zfp462 is an important factor involved in cell division during the early embryonic development of vertebrates. In pluripotent P19 cells, ZFPIP/Zfp462 takes part in cell proliferation, likely via its role in maintaining chromatin structure. To further define the function of ZFPIP/Zfp462 in the mechanisms of pluripotency and cell differentiation, we constructed a stable P19 cell line in which ZFPIP/Zfp462 knockdown is inducible. We report that ZFPIP/Zfp462 was vital for mitosis and self-renewal in pluripotent P19 cells. Its depletion induced substantial decreases in the expression of the pluripotency genes Nanog, Oct4 and Sox2 and was associated with the transient expression of specific neuronal differentiation markers. We also demonstrated that ZFPIP/Zfp462 expression appears to be unnecessary after neuronal differentiation is induced in P19 cells. Taken together, our results strongly suggest that ZFPIP/Zfp462 is a key chromatin factor involved in maintaining P19 pluripotency and in the early mechanisms of neural differentiation but that it is dispensable in differentiated P19 cells.
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