Cell Surface Changes During the Egg-to-Embryo Transition

卵子到胚胎转变过程中细胞表面的变化

基本信息

  • 批准号:
    7931221
  • 负责人:
  • 金额:
    $ 1.2万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2009
  • 资助国家:
    美国
  • 起止时间:
    2009-09-30 至 2010-09-29
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): If fertilized, all eggs undergo an egg-to-embryo transition. Within minutes or hours of insemination, depending on the animal, the egg shuffles its existing molecular machinery and transforms itself into a cell with vastly different developmental potential. The first mechanistic alteration of this egg-to-embryo transition establishes the block to polyspermy, which is followed by and integrated with the turnover of maternal mRNA and cytoplasmic proteins, altered signal transduction capabilities, and changes at the cell surface including the addition and removal of specific membrane proteins and lipids. This transition is independent of new transcriptional activity, and for technical reasons, a majority of recent research towards understanding the egg-to-embryo transition has focused on signal transduction mechanisms and changes in mRNAs. The sea urchin and starfish, however, offer an opportunity to examine the changes that occur specifically at the cell surface. While the details of this process differ among animals, as with much of the reproductive phenomena, all eggs undergo this general transition. We will take advantage of the sea urchin and starfish because 1) millions of oocytes, eggs and embryos are readily obtained; 2) all the major proteins of the cortical granules have been defined; 3) the egg and oocyte plasma membrane can be manipulated experimentally in many ways; and 4) the genome sequence and genomic resources from the sea urchin Strongylocentrotus purpuratus are available. Results of this study will elucidate conserved mechanisms of this major developmental transition in all animals. Furthermore, because the changes examined here are at the cell surface, they will help clinicians develop new methods to non-invasively assess developmental potential in IVF applications for humans. PUBLIC HEALTH RELEVANCE: Immediately after fertilization, the egg rapidly transforms into an embryo with many new biochemical, cellular, and developmental features. This essential change is programmed into the egg and is independent of new gene expression; i.e., they reflect changes of the existing molecular machinery. Our research focuses on the changes that occur on the cell surface of the egg to embryo transition. These are some of the most rapid and conserved changes that occur in embryos and are detectable from the outside of the cell. Thus, this research will lead to a better understanding of a major transition in fertilization and development of all animals, and to the identification of non invasive, early markers indicative of successful development. Our results will have particular significance to clinical IVF predictions in human reproductive health.
描述(由申请人提供):如果受精,所有的卵子都经历了卵子到胚胎的转变。在授精后的几分钟或几小时内,取决于动物,卵子改组其现有的分子机制,并将自己转变为具有截然不同的发育潜力的细胞。这种卵-胚胎转变的第一个机制改变建立了多精受精的阻断,随后是母体mRNA和细胞质蛋白的周转,改变的信号转导能力,以及细胞表面的变化,包括特定膜蛋白和脂质的添加和去除。这种转变独立于新的转录活性,并且由于技术原因,大多数最近的研究都集中在了解卵子到胚胎的转变的信号转导机制和mRNA的变化。然而,海胆和海星提供了一个检查细胞表面发生的变化的机会。虽然这一过程的细节在动物中各不相同,但正如许多生殖现象一样,所有的卵子都经历了这一普遍的转变。我们将利用海胆和海星,因为1)数百万的卵母细胞,卵子和胚胎很容易获得; 2)皮质颗粒的所有主要蛋白质都已被定义; 3)卵子和卵母细胞质膜可以通过多种方式进行实验操作; 4)来自海胆的基因组序列和基因组资源是可用的。这项研究的结果将阐明所有动物的这一主要发育转变的保守机制。此外,由于这里检查的变化是在细胞表面,它们将帮助临床医生开发新的方法来非侵入性地评估人类IVF应用中的发育潜力。公共卫生相关性:受精后,卵子迅速转变为具有许多新的生化,细胞和发育特征的胚胎。这种基本的变化被编程到卵子中,并且不依赖于新的基因表达;即,它们反映了现有分子机制的变化。我们的研究重点是发生在卵子到胚胎过渡的细胞表面上的变化。这些是胚胎中发生的最快速和最保守的变化,可以从细胞外部检测到。因此,这项研究将有助于更好地了解所有动物受精和发育的主要转变,并确定指示成功发育的非侵入性早期标记。我们的研究结果将对人类生殖健康的临床IVF预测具有特殊意义。

项目成果

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科研奖励数量(0)
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GARY M WESSEL其他文献

GARY M WESSEL的其他文献

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{{ truncateString('GARY M WESSEL', 18)}}的其他基金

Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10797823
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10624736
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10472183
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10397891
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10725044
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10414946
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
  • 批准号:
    10631065
  • 财政年份:
    2021
  • 资助金额:
    $ 1.2万
  • 项目类别:
Sequential restriction of germ line progenitors by induction
通过诱导连续限制种系祖细胞
  • 批准号:
    9980947
  • 财政年份:
    2019
  • 资助金额:
    $ 1.2万
  • 项目类别:
2015 Fertilization and Activation of Development Gordon Research Conference & Gordon Research Seminar
2015年施肥与发育激活戈登研究会议
  • 批准号:
    8975378
  • 财政年份:
    2015
  • 资助金额:
    $ 1.2万
  • 项目类别:
Single Nucleotide Genome Modifications in Oocytes
卵母细胞中的单核苷酸基因组修饰
  • 批准号:
    8691207
  • 财政年份:
    2014
  • 资助金额:
    $ 1.2万
  • 项目类别:

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