THE MAINTENANCE OF FETAL MATERNAL TOLERANCE IN MARSUPIALS

有袋动物胎儿母体耐受性的维持

基本信息

  • 批准号:
    7382029
  • 负责人:
  • 金额:
    $ 10.15万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2006
  • 资助国家:
    美国
  • 起止时间:
    2006-07-01 至 2007-06-30
  • 项目状态:
    已结题

项目摘要

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. One of the remaining enigmas in immunology is the ability of the fetus to escape rejection by the maternal immune system despite antigenic differences in the embryo contributed by paternal alleles. It is clear from studies in placental mammals, humans in particular, that the maternal immune system is "aware" of the fetal antigens as foreign. How the maternal immune system is regulated to prevent rejection of fetal, specifically placental tissues, is not completely understood. A novel approach to understanding the problem of how fetal-maternal tolerance is maintained is to ask, "what mechanisms appeared during mammalian evolution to adapt the immune system to tolerate an allogeneic placenta?" This question can only be answered through comparative analysis of mammalian fetal-maternal interactions. In this proposal we are using marsupials as the alternative models of evolution of mammalian reproduction. Two species of marsupials are used in this study; the South American opossum, Monodelphis domestica, which has a simple yolk sac placenta and the Northern brown bandicoot, Isoodon macrourus, which has a chorio-allantoic placenta, not unlike eutherian mammals such as humans and mice. These two species should provide interesting insights into how different levels of placentation affect mechanisms of fetal-maternal tolerance. This study takes advantage of the NIH funded whole genome sequence of M. domestica.
该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者(PI)可能从另一个NIH来源获得主要资金,因此可以在其他CRISP条目中表示。所列机构为中心机构,不一定为研究者机构。免疫学中剩下的一个谜团是,尽管胚胎中的抗原差异是由父亲的等位基因贡献的,但胎儿仍有能力逃避母体免疫系统的排斥。从胎盘哺乳动物,特别是人类的研究中可以清楚地看出,母体免疫系统“知道”胎儿抗原是外来的。如何调节母体免疫系统以防止胎儿,特别是胎盘组织的排斥,还没有完全了解。一种新的方法来理解胎儿-母体耐受性是如何维持的问题是问,“在哺乳动物进化过程中出现了什么机制来适应免疫系统以耐受同种异体胎盘?“这个问题只能通过对哺乳动物胎儿-母体相互作用的比较分析来回答。在这个建议中,我们使用有袋动物作为哺乳动物生殖进化的替代模型。本研究中使用了两种有袋动物:南美洲负鼠(Monodelphis astritica),它有一个简单的卵黄囊胎盘;北方棕色袋狸(Isodon macrourus),它有一个绒毛膜-尿囊胎盘,与人类和小鼠等真兽目哺乳动物没有什么不同。这两个物种应该提供有趣的见解如何不同水平的胎盘影响机制的胎儿-母亲的耐受性。本研究利用NIH资助的M.南极洲

项目成果

期刊论文数量(0)
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MICHELLE L BAKER其他文献

MICHELLE L BAKER的其他文献

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{{ truncateString('MICHELLE L BAKER', 18)}}的其他基金

SHINING A LIGHT ON BAT CELLULAR IMMUNITY FOLLOWING VIRUS INFECTION
揭示病毒感染后蝙蝠细胞免疫
  • 批准号:
    10449406
  • 财政年份:
    2022
  • 资助金额:
    $ 10.15万
  • 项目类别:
SHINING A LIGHT ON BAT CELLULAR IMMUNITY FOLLOWING VIRUS INFECTION
揭示病毒感染后蝙蝠细胞免疫
  • 批准号:
    10618969
  • 财政年份:
    2022
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE INTERFERON RESPONSE OF A MODEL CHIROPTERAN BAT; THE BLACK FLYING FOX, PTEROP
翼手目蝙蝠模型的干扰素反应;
  • 批准号:
    8360211
  • 财政年份:
    2011
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE INTERFERON RESPONSE OF A MODEL CHIROPTERAN BAT; THE BLACK FLYING FOX, PTEROP
翼手目蝙蝠模型的干扰素反应;
  • 批准号:
    8168271
  • 财政年份:
    2010
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE MAINTENANCE OF FETAL MATERNAL TOLERANCE IN MARSUPIALS
有袋动物胎儿母体耐受性的维持
  • 批准号:
    7960516
  • 财政年份:
    2009
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE MAINTENANCE OF FETAL MATERNAL TOLERANCE IN MARSUPIALS
有袋动物胎儿母体耐受性的维持
  • 批准号:
    7610561
  • 财政年份:
    2007
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE MAINTENANCE OF FETAL MATERNAL TOLERANCE IN MARSUPIALS
有袋动物胎儿母体耐受性的维持
  • 批准号:
    7171260
  • 财政年份:
    2005
  • 资助金额:
    $ 10.15万
  • 项目类别:
THE MAINTENANCE OF FETAL MATERNAL TOLERANCE IN MARSUPIALS
有袋动物胎儿母体耐受性的维持
  • 批准号:
    6981926
  • 财政年份:
    2004
  • 资助金额:
    $ 10.15万
  • 项目类别:

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母体细胞外囊泡是妊娠并发 1 型糖尿病时胎儿生长和后代心脏代谢健康的关键介质。
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