Levine R A, Campisi J, Wang S Y, Gudas L J
Dev Biol. 1984 Oct;105(2):443-50. doi: 10.1016/0012-1606(84)90301-4.
F9 mouse teratocarcinoma stem cells differentiate into parietal endoderm cells in the presence of retinoic acid, dibutyryl cyclic AMP, and theophylline (RACT). When F9 cells are exposed to 2-5 mM sodium butyrate plus RACT, they fail to differentiate. Differentiation is assessed by induction of laminin and collagen IV mRNA, the synthesis of laminin, collagen IV and plasminogen activator proteins, and alterations in cell morphology. Butyrate inhibits differentiation only when added within 8 hr after retinoic acid addition. Thus an early event in retinoid action on F9 cells is butyrate-sensitive. The population doubling time and cell cycle distribution of F9 cells are not altered within the first 24 hr after butyrate addition, suggesting that butyrate does not inhibit differentiation by inhibition of growth or normal cycling. However, butyrate does inhibit histone deacetylation in F9 cells, and this could be the mechanism by which butyrate inhibits differentiation.
在视黄酸、二丁酰环磷腺苷和茶碱(RACT)存在的情况下,F9小鼠畸胎瘤干细胞可分化为滋养层内胚层细胞。当F9细胞暴露于2 - 5 mM丁酸钠加RACT时,它们无法分化。通过诱导层粘连蛋白和IV型胶原mRNA、层粘连蛋白、IV型胶原和纤溶酶原激活蛋白的合成以及细胞形态的改变来评估分化情况。丁酸盐仅在视黄酸添加后8小时内添加时才会抑制分化。因此,类视黄醇对F9细胞作用的早期事件对丁酸盐敏感。丁酸盐添加后的头24小时内,F9细胞的群体倍增时间和细胞周期分布未发生改变,这表明丁酸盐不是通过抑制生长或正常细胞周期来抑制分化的。然而,丁酸盐确实会抑制F9细胞中的组蛋白去乙酰化,这可能是丁酸盐抑制分化的机制。