DNA Demethylation and BKca Channel Expression and Function in Uterine Arteries

子宫动脉中 DNA 去甲基化和 BKca 通道表达和功能

• 批准号: 9020248
• 负责人: Lubo Zhang
• 金额: $ 19.55万
• 依托单位: LOMA LINDA UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-03-01 至 2018-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9020248
• 关键词: Adult; Arteries; Blood Vessels; Blood flow; Cardiovascular system; Clinical; Clinical Management; DNA; DNA Methylation; Down-Regulation; Employee Strikes; Epigenetic Process; Fetal Development; Fetal Growth Retardation; Fetus; Functional disorder; Gene Expression Profile; Genes; Growth; Health; Hormones; Hydroxylation; Incidence; Investigation; Knowledge; Lead; Maternal Health; Mediating; Methylation; Modification; Molecular; Mothers; Muscle function; Outcome; Personal Satisfaction; Physiology; Play; Pre-Eclampsia; Pregnancy; Pregnancy Complications; Promoter Regions; Proteins; Repression; Research; Role; Series; Sheep; Testing; Time; Tissues; Up-Regulation; Uteroplacental Circulation; Vascular Smooth Muscle; demethylation; epigenetic regulation; fetal; gene repression; improved; inhibitor/antagonist; innovation; insight; neonatal outcome; novel; perinatal morbidity; pregnant; pressure; promoter; research study; steroid hormone; stoichiometry; vascular bed

 DESCRIPTION (provided by applicant): The striking increase of uterine blood flow during pregnancy is essential both for optimal growth of the fetus and cardiovascular well-being of the mother. Maladaptation of the uteroplacental circulation during gestation is associated with high incidence of clinical complications including preeclampsia and fetal development abnormality. Large-conductance Ca2+-activated K+ (BKCa) channels play a critical role in regulating uterine blood flow in pregnancy. Recent studies in sheep demonstrated that pregnancy and steroid hormones caused a significant increase in BKCa β1 subunit resulting in increased β1:α subunit stoichiometry and heightened BKCa channel activity in uterine arteries. Yet the molecular mechanisms remain unknown. Our preliminary studies showed that pregnancy and steroid hormones caused a decrease in DNA methylation at the β1 gene promoter. DNA methylation is a chief mechanism in epigenetic repression of gene expression patterns. Recent studies suggest a robust mechanism of ten-eleven translocation 1-3 (TET1-3) proteins in active DNA demethylation. Preliminary studies suggested that pregnancy and steroid hormones increased TET1-2 expression in uterine arteries. These findings lead to the proposed studies of a highly novel mechanism testing the hypothesis that steroid hormone-mediated dynamic changes of DNA methylation and demethylation play a key role in regulating expression and function of BKCa channels in uterine vascular adaptation to pregnancy. Two specific aims will determine whether: 1) steroid hormone-mediated promoter demethylation and BKCa β1 gene up- regulation play a causal role in increased BKCa channel function in uterine arteries in pregnancy, and 2) steroid hormone-mediated up-regulation of TET1-3 plays a causal role in active DNA demethylation and the β1 gene up-regulation in pregnancy. The proposed study presents a major breakthrough and paradigm-shifting focus of research aiming at unraveling highly novel epigenetic mechanisms of hormone-mediated DNA demethylation in regulating gene expression patterns in uterine vasculature in particular, and in vascular smooth muscle function in general. The outcome of the proposed study will significantly advance our knowledge in molecular mechanisms of uteroplacental adaptation to pregnancy and improve our understanding of pathophysiological mechanisms underlying maladaptation of uteroplacental circulation and pregnancy complications. Because of the vital importance of BKCa channel function in regulating vascular tone and pressure in virtually all vascular beds, and the extremely limited knowledge in epigenetic regulation of BKCa channel expression and activity in vascular smooth muscle, the proposed study will indeed have a much broad impact in comprehensive understanding of molecular mechanisms in regulating BKCa channel activity and vascular function in physiology and pathophysiology.