Department of Comparative Biomedical Sciences, Royal Veterinary College, University of London, 4 Royal College Street, London NW1 0TU, UK.
National Heart and Lung Institute, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UK.
Cells. 2023 Jul 28;12(15):1957. doi: 10.3390/cells12151957.
MicroRNAs (miRNAs) are important regulators of embryonic stem cell (ESC) biology, and their study has identified key regulatory mechanisms. To find novel pathways regulated by miRNAs in ESCs, we undertook a bioinformatics analysis of gene pathways differently expressed in the absence of miRNAs due to the deletion of , which encodes an RNase that is essential for the synthesis of miRNAs. One pathway that stood out was Ca signaling. Interestingly, we found that ESCs had no difference in basal cytoplasmic Ca levels but were hyperresponsive when Ca import into the endoplasmic reticulum (ER) was blocked by thapsigargin. Remarkably, the increased Ca response to thapsigargin in ESCs resulted in almost no increase in apoptosis and no differences in stress response pathways, despite the importance of miRNAs in the stress response of other cell types. The increased Ca response in ESCs was also observed during purinergic receptor activation, demonstrating a physiological role for the miRNA regulation of Ca signaling pathways. In examining the mechanism of increased Ca responsiveness to thapsigargin, neither store-operated Ca entry nor Ca clearance mechanisms from the cytoplasm appeared to be involved. Rather, it appeared to involve an increase in the expression of one isoform of the IP receptors (). miRNA regulation of expression primarily appeared to be indirect, with transcriptional regulation playing a major role. Therefore, the miRNA regulation of expression offers a unique mechanism to regulate Ca signaling pathways in the physiology of pluripotent stem cells.
微小 RNA(miRNAs)是胚胎干细胞(ESC)生物学的重要调节因子,其研究确定了关键的调节机制。为了发现 miRNA 在 ESC 中调控的新途径,我们对由于编码一种对于 miRNA 合成至关重要的 RNase 的缺失而导致 miRNA 缺失时差异表达的基因途径进行了生物信息学分析。一条引人注目的途径是 Ca 信号转导。有趣的是,我们发现,尽管 miRNA 在其他细胞类型的应激反应中很重要,但在基础细胞质 Ca 水平上,缺失型 ESC 与野生型 ESC 没有差异,但当内质网(ER)中 Ca 内流被 thapsigargin 阻断时,它们的反应性就会增强。值得注意的是,尽管 miRNA 在其他细胞类型的应激反应中很重要,但缺失型 ESC 对 thapsigargin 的 Ca 反应增加导致几乎没有凋亡增加,也没有应激反应途径的差异。缺失型 ESC 对 thapsigargin 的 Ca 反应增加也在嘌呤能受体激活期间观察到,这表明 miRNA 对 Ca 信号通路的调控具有生理作用。在研究对 thapsigargin 反应性增加的机制时,既没有涉及到储存操作的 Ca 内流,也没有涉及到从细胞质中清除 Ca 的机制。相反,它似乎涉及到一种 IP 受体()的一种同工型的表达增加。miRNA 对 表达的调控主要是间接的,转录调控起着主要作用。因此,miRNA 对 表达的调控为调节多能干细胞生理学中 Ca 信号通路提供了一种独特的机制。