Embryonic Gene Expression During Diabetic Embryopathy

项目概述：糖尿病胚胎病是一种糖尿病并发症，糖尿病母亲的早期胚胎出现先天性畸形。提出的实验采用糖尿病妊娠小鼠模型，其中控制基本发育过程的基因表达受到干扰。这些实验的重点是Pax3，一个在糖尿病小鼠胚胎中表达显著降低的基因，该基因编码一种转录因子，这种转录因子在糖尿病胚胎病中经常畸形的结构发育中是必需的，尤其是神经管和心脏。在之前的资助期内，我们发现母体高血糖增加了胚胎的葡萄糖输送，过量的葡萄糖代谢引起的氧化和缺氧应激导致Pax3表达受损，从而导致神经管缺陷（NTD）。除了使用胚胎进行实验外，我们还使用了小鼠胚胎干细胞（ES），这种细胞可以大量生长，并且可以诱导为表达pax3的神经上皮细胞类型。本研究的核心假设是，受早期胚胎葡萄糖代谢增加影响的生化途径会导致氧化和缺氧应激，从而阻止转录因子的诱导或结合，从而激活必要的发育控制基因的表达。在这个提案中，我们将：(1)研究缺氧应激、氧化应激和蛋白激酶C活性升高导致Pax3表达受损的相互作用；(2)确定与Pax3调控元件结合的因子，该元件是分化诱导表达所必需的，并且被氧化应激抑制；(3)验证导致小鼠ES细胞中Pax3表达受损的生化干扰同样会导致人类ES细胞中Pax3表达受损的假设。相关性：了解母体糖尿病如何在生化和分子水平上干扰早期胚胎发育是必要的，以便制定新的策略来预防它们。该研究将使用小鼠糖尿病妊娠模型和小鼠胚胎干细胞来阐明重要胚胎基因表达受到干扰的生化机制，并使用人类胚胎干细胞来确定小鼠和小鼠干细胞在多大程度上作为人类糖尿病妊娠期间生化干扰影响的模型。

DESCRIPTION (provided by applicant): Project Summary: Diabetic embryopathy is a diabetic complication in which the early embryo of a mother with diabetes develops congenital malformations. The proposed experiments employ a mouse model of diabetic pregnancy in which expression of genes which control essential developmental processes is disturbed. These experiments focus on Pax3, a gene whose expression is significantly reduced in embryos of diabetic mice, which encodes a transcription factor required for development of structures that are often malformed during diabetic embryopathy, especially the neural tube and the heart. In the previous funding period, we showed that maternal hyperglycemia increases glucose delivery to the embryo, and that oxidative and hypoxic stress, resulting from excess glucose metabolism, causes impaired Pax3 expression, thereby leading to neural tube defects (NTD). In addition to experiments using embryos, we have used murine embryonic stem (ES) cells, which can be grown in quantity and can be induced to a Pax3-expressing neuroepithelial cell type. The central hypothesis to be tested in this proposal is that biochemical pathways affected by increased glucose metabolism by the early embryo causes oxidative and hypoxic stress, which prevents the induction or binding of transcription factors that activate expression of essential developmental control genes. In this proposal we will: (1) Investigate the interaction of hypoxic stress, oxidative stress, and increased protein kinase C activity leading to impaired Pax3 expression; (2) Identify factors which bind to a Pax3 regulatory element that is needed for differentiation-induced expression and which is inhibited by oxidative stress; and (3) Test the hypothesis that the same biochemical disturbances that lead to impaired Pax3 expression in mouse ES cells also lead to impaired PAX3 expression in human ES cells. Relevance: Understanding how maternal diabetes disturbs early embryonic development on a biochemical and molecular level is essential in order to devise new strategies to prevent them. The proposed research will use a mouse model of diabetic pregnancy and mouse embryonic stem cells to elucidate the biochemical mechanisms by which important embryonic gene expression is disturbed, and human embryonic stem cells to determine the extent to which the mouse and mouse stem cells serve as a model for the effects of biochemical disturbances during human diabetic pregnancy.