Mechanisms of fetal intestinal stem cell regulation and maturation
Mechanisms of fetal intestinal stem cell regulation and maturation
批准号:
8918614
负责人:
Jason Spence
金额:
$33.98万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-01 至 2019-08-31
关键词:
AdultAffectAnimalsBindingBiological ModelsCellsChromatinConflict (Psychology)DataDevelopmentDiseaseDistalEmbryoEpigenetic ProcessEpithelialEventG-Protein-Coupled ReceptorsGene Expression ProfileGenesGeneticGoalsGrowthHealthHumanIn VitroIntestinal AtresiaIntestinesLabelLifeLigandsLinkLiteratureMesenchymalModelingMolecularMusNeonatalOrganoidsPluripotent Stem CellsPopulationProcessRegulationRegulator GenesRoleShort Bowel SyndromeSignal TransductionSmall IntestinesStagingStem cellsSystemTestingTimeTissuesTransgenic Organismsadult stem cellbaseembryonic stem cellepigenomeepigenomicsfetalgain of functionhuman embryonic stem cellhuman embryonic stem cell linein vitro Modelin vivomouse modelnovelprogenitorregenerativeresearch studystemstemnesstranscription factor
中文摘要
描述(申请人提供):胚胎肠干细胞调控和成熟的机制胚胎祖细胞和成体组织特异性干细胞的调控已被深入研究。然而,这些群体(胚胎祖细胞与成体干细胞)通常被认为是存在于时间和空间中的离散实体。例如,人们一致认为胎儿肠祖细胞产生成人肠上皮细胞,但一些文献表明,成人肠干细胞在隐窝形成过程中从头出现,并且在分子上与其胚胎前辈不同。然而,我们的初步观察表明,在胎儿/胚胎肠,成人肠干细胞基因的表达和维持在整个发展/分化的细胞亚群。基于这些结果,我们假设“成体干细胞”状态不是一个离散事件,而是发育连续体的一部分。也就是说,“干/祖”状态在胚胎肠细胞亚群中发育建立,产生成体肠干细胞。为了检验我们的假设,我们将利用两个模型系统,小鼠模型系统和人多能干细胞衍生的肠组织。结合起来,这些强大的体内和体外系统将使我们能够研究遗传和表观遗传
肠干细胞前体和成体肠干细胞的个体发生。
英文摘要
DESCRIPTION (provided by applicant): Mechanisms of fetal intestinal stem cell regulation and maturation Regulation of embryonic progenitor cells and adult tissue-specific stem cells has been intensely studied. However, these populations (embryonic progenitor vs. adult stem cell) are often considered to be discrete entities existing within time and space. For example, it is uniformly accepted that fetal intestinal progenitor cells give rise to the adult intestinal epithelum, but some literature suggests that adult intestinal stem cells emerge de novo during crypt formation and are molecularly distinct from their embryonic predecessors. However, our preliminary observations suggest that in the fetal/embryonic intestine, adult intestinal stem cell genes are expressed and maintained in a subset of cells throughout development/differentiation. Based on these results, we hypothesize that the "adult stem cell" state is not a discrete event, but part of a developmental continuum. That is, a "stem/progenitor" state is established developmentally in a subset of embryonic intestinal cells that give rise to adult intestinal stem cells. To test our hypothesis we will take advantage of two model systems, the murine model system and human pluripotent stem cell derived intestinal tissue. Combined, these powerful in vivo and in vitro systems will allow us to investigate the genetic and epigenetic
ontogeny of intestinal stem cell precursors and adult intestinal stem cells.
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海外基金