Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Isotope Science Center, The University of Tokyo, Tokyo, Japan.
Biochem Biophys Res Commun. 2020 Mar 26;524(1):57-63. doi: 10.1016/j.bbrc.2019.12.098. Epub 2020 Jan 22.
In normal development, the rate of cell differentiation is tightly controlled and critical for normal development and stem cell differentiation. However, the underlying mechanisms regulating the rate of the differentiation are unknown, and manipulation of the rate of the stem cell differentiation is currently difficult. Here we show that activation of protein kinase A (PKA) accelerates the rate of mouse embryonic stem cell (ESC) differentiation through an early loss of ESC pluripotency markers and early appearance of mesodermal and other germ layer cells. The activation of PKA hastened differentiation by increasing the expression of a histone H3 lysine 9 (H3K9) dimethyltransferase, G9a protein, and the level of a negative epigenetic histone mark, H3K9 dimethylation (H3K9me2), in the promoter regions of the pluripotency markers Nanog and Oct4. These results elucidate a novel role of PKA on ESC differentiation and offer an experimental model for controlling the rate of ESC differentiation.
在正常发育过程中,细胞分化的速度受到严格控制,这对正常发育和干细胞分化至关重要。然而,调节分化速度的潜在机制尚不清楚,目前难以操纵干细胞分化的速度。在这里,我们表明蛋白激酶 A(PKA)的激活通过早期失去胚胎干细胞(ESC)多能性标志物和早期出现中胚层和其他胚层细胞来加速小鼠胚胎干细胞(ESC)的分化速度。PKA 的激活通过增加组蛋白 H3 赖氨酸 9(H3K9)二甲基转移酶、G9a 蛋白的表达以及多能性标志物 Nanog 和 Oct4 启动子区域中负表观遗传组蛋白标记 H3K9 二甲基化(H3K9me2)的水平,加速了分化。这些结果阐明了 PKA 在 ESC 分化中的新作用,并为控制 ESC 分化速度提供了一个实验模型。