Regulation of Angiogenesis in Mammalian Ovaries
Regulation of Angiogenesis in Mammalian Ovaries
批准号:
RGPIN-2015-03753
负责人:
Petrik, Jim
金额:
$1.75万
依托单位:
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2019
资助国家:
加拿大
项目状态:
已结题
起止时间:
2019-01-01 至 2020-12-31
中文摘要
我实验室的长期目标是了解家畜卵巢功能的生物学,以及卵巢功能障碍如何导致生殖障碍和不孕。* 该项目的短期目标是确定小RNA在调节卵巢血管形成和卵泡及黄体发育中的作用。我的实验室在研究调节卵巢血管形成的因素以及这些因素如何影响正常和异常的卵巢功能方面处于领先地位。 我们是第一个描述在整个卵巢周期中促血管生成因子和抗血管生成因子之间的复杂关系,以及这种关系如何促进卵泡和黄体发育的人。特别是,我们已经全面描述了血管内皮生长因子(VEGF)和血小板反应蛋白-1(TSP-1)家族在调节卵巢血管生成、卵泡和黄体发育以及生育力方面的作用。 在这个提议中,我们描述了一种方法来研究microRNA在介导卵巢血管生成,发育和功能相关因子表达中的作用,以及miRNAs如何参与卵巢生殖疾病,如牛的囊性卵巢病(COD)。 miRNA是小的非编码RNA,其通过靶向信使RNA(mRNA)的3'非翻译(3' UTR)在转录后抑制基因表达,并且已经显示出调节许多关键生物过程。 microRNA对基因表达具有重要的控制作用,因为单个miRNA可以靶向多个mRNA,而多个miRNA也可以靶向单个mRNA。我们假设miRNA是调节卵巢功能的组成部分,并协调卵巢血管生成和卵泡发育,并且改变的miRNA表达有助于牛卵巢功能障碍和生殖障碍的发生和进展。我们的研究计划分为三个主要目的来验证这一假设。 目标1。 鉴定参与调节卵巢血管生成的microRNA的表达。目标二。评估microRNA在调节卵巢血管生成、卵泡和黄体发育中的作用。 目标3:确定microRNAs在卵巢相关生殖疾病中的作用 *影响:这些研究结果将为卵巢血管生成、卵泡和黄体发育的生物学机制提供新的数据。虽然已经描述了促血管生成因子和抗血管生成因子表达的变化,但目前对这些因子如何调节,特别是它们如何抑制彼此的表达缺乏了解。这些研究的数据将阐明miRNA在调节卵巢血管生成中的作用,以及它们如何促进正常卵巢功能和卵巢病理学,如牛的COD。**
英文摘要
TheLong Term Objective of my lab is to understand the biology of ovarian function in domestic animals and how ovarian dysfunction can contribute to reproductive disorders and infertility. ***The Short Term Objective of this program is to identify the role of small RNAs in regulating blood vessel formation and follicle and luteal development in the ovary.***My laboratory has been a leader in the study of factors that regulate blood vessel formation in the ovary and how these factors contribute to normal and abnormal ovarian function. We were the first to describe the intricate relationship between pro- and anti-angiogenic factors throughout the ovarian cycle, and how this relationship contributes to follicular and luteal development. In particular, we have comprehensively described the roles of the vascular endothelial growth factor (VEGF) and thrombospondin-1 (TSP-1) families in regulating ovarian angiogenesis, follicular and luteal development, and fertility. In this proposal, we describe an approach to study the role of microRNAs in mediating the expression of factors related to ovarian angiogenesis, development, and function, and how miRNAs may be involved in ovarian-based reproductive disorders such as cystic ovarian disease (COD) in cattle. MiRNAs are small, non-coding RNAs that repress gene expression post-transcriptionally by targeting 3' untranslated (3'UTRs) of messenger RNAs (mRNAs) and have been shown to regulate a host of critical biological processes. MicroRNAs have significant control over gene expression, as a single miRNA can target multiple mRNAs, and multiple miRNAs may also target a single mRNA.***We hypothesize that miRNAs are integral to the regulation of ovarian function and coordinate ovarian angiogenesis and follicular development, and altered miRNA expression contributes to the onset and progression of ovarian dysfunction and reproductive disorders in bovines.***Our research program is organized into three main Aims to test this hypothesis. Aim 1. Identify the expression of microRNAs involved in regulating ovarian angiogenesis. Aim 2. Evaluate the role of microRNAs in regulating ovarian angiogenesis, and follicular and luteal development. Aim 3. Determine the role of microRNAs in ovarian-based reproductive disorders.***Impact: The results from these studies will provide new data about the biological mechanisms that regulate ovarian angiogenesis and follicular and luteal development. Although changes in expression of pro- and anti-angiogenic factors have been described, there currently is a significant lack of understanding of how these factors are regulated, particularly in how they reciprocally inhibit each other's expression. The date from these studies will illuminate the roles of miRNAs in regulation ovarian angiogenesis and how they contribute to normal ovarian function and ovarian pathologies such as COD in cattle. **
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会议论文
Regulation of Angiogenesis in Mammalian Ovaries
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批准号:RGPIN-2015-03753
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项目类别:Discovery Grants Program - Individual
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资助金额:$1.75万
-
财政年份:2018
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负责人:Petrik, Jim
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依托单位:
Regulation of Angiogenesis in Mammalian Ovaries
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批准号:RGPIN-2015-03753
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项目类别:Discovery Grants Program - Individual
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资助金额:$1.75万
-
财政年份:2017
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负责人:Petrik, Jim
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依托单位:
Regulation of Angiogenesis in Mammalian Ovaries
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批准号:RGPIN-2015-03753
-
项目类别:Discovery Grants Program - Individual
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资助金额:$1.75万
-
财政年份:2016
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负责人:Petrik, Jim
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依托单位:
Regulation of Angiogenesis in Mammalian Ovaries
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批准号:RGPIN-2015-03753
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项目类别:Discovery Grants Program - Individual
-
资助金额:$1.75万
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财政年份:2015
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负责人:Petrik, Jim
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依托单位:
国内基金
海外基金
ROBO4对视网膜血管生成(angiogenesis)的调控及其分子机制
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批准号:81200692
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2012
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负责人:陈凌
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依托单位: