Cell Biology Group, Department of Surgery, University of Maryland School of Medicine , Baltimore, Maryland.
Baltimore Veterans Affairs Medical Center , Baltimore, Maryland.
Am J Physiol Cell Physiol. 2019 Mar 1;316(3):C415-C423. doi: 10.1152/ajpcell.00165.2018. Epub 2019 Jan 16.
Both zipcode binding protein-1 (ZBP1) and phospholipase C-γ1 (PLCγ1) are intimately involved in many aspects of early intestinal mucosal repair after acute injury, but the exact mechanisms that control their cellular abundances remain largely unknown. The present study shows that microRNA-222 (miR-222) interacts with the mRNAs encoding ZBP1 and PLCγ1 and regulates ZBP1 and PLCγ1 expression in intestinal epithelial cells (IECs). The biotinylated miR-222 bound specifically to the ZBP1 and PLCγ1 mRNAs in IECs. Ectopically expressed miR-222 precursor destabilized the ZBP1 and PLCγ1 mRNAs and consequently lowered the levels of cellular ZBP1 and PLCγ1 proteins. Conversely, decreasing the levels of cellular miR-222 by transfection with its antagonism increased the stability of the ZBP1 and PLCγ1 mRNAs and increased the levels of ZBP1 and PLCγ1 proteins. Overexpression of miR-222 also inhibited cell migration over the wounded area, which was partially abolished by overexpressing ZBP1 and PLCγ1. Furthermore, prevention of the increased levels of ZBP1 and PLCγ1 in the miR-222-silenced cells by transfection with specific small interfering RNAs targeting ZBP1 or PLCγ1 mRNA inhibited cell migration after wounding. These findings indicate that induced miR-222 represses expression of ZBP1 and PLCγ1 at the posttranscriptional level, thus inhibiting IEC migration during intestinal epithelial restitution after wounding.
锌指蛋白结合蛋白 1(ZBP1)和磷脂酶 C-γ1(PLCγ1)均密切参与急性损伤后早期肠道黏膜修复的多个方面,但控制其细胞丰度的确切机制仍知之甚少。本研究表明,微小 RNA-222(miR-222)与编码 ZBP1 和 PLCγ1 的 mRNAs 相互作用,并调节肠上皮细胞(IECs)中的 ZBP1 和 PLCγ1 表达。生物素标记的 miR-222 特异性结合到 IECs 中的 ZBP1 和 PLCγ1 mRNAs。异位表达的 miR-222 前体使 ZBP1 和 PLCγ1 mRNAs 不稳定,从而降低细胞内 ZBP1 和 PLCγ1 蛋白水平。相反,通过转染其拮抗剂降低细胞内 miR-222 的水平增加了 ZBP1 和 PLCγ1 mRNAs 的稳定性,并增加了 ZBP1 和 PLCγ1 蛋白的水平。miR-222 的过表达也抑制了细胞在受伤区域的迁移,而过表达 ZBP1 和 PLCγ1 则部分消除了这种抑制作用。此外,通过转染针对 ZBP1 或 PLCγ1 mRNA 的特异性小干扰 RNA 防止 miR-222 沉默细胞中 ZBP1 和 PLCγ1 水平的增加,抑制了创伤后细胞的迁移。这些发现表明,诱导的 miR-222 在转录后水平抑制 ZBP1 和 PLCγ1 的表达,从而抑制创伤后肠道上皮修复过程中 IEC 的迁移。