课题基金 / 基金详情

Origin and Fate of Myogenic Stem Cells

Origin and Fate of Myogenic Stem Cells
肌源干细胞的起源和命运
批准号:
6848295
负责人:
MINDY GEORGE-WEINSTEIN
金额:
$19.64万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-03-01 至 2007-02-28

项目摘要

项目成果

MINDY GEORGE-WEINSTEIN的其他基金

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中文摘要
翻译
描述(申请人提供):未分化的干细胞存在于成年机体中。在大多数情况下,尚不清楚这些细胞是否能够沿着多条途径分化,或者是否被编程为沿着一条途径发展。此外,成体干细胞的来源尚不清楚。下面的研究重点是肌源性干细胞。在这些实验中要检验的一般假设是,致力于骨骼肌谱系的干细胞:(1)存在于早期鸡胚胎的外胚层中,(2)在原肠形成过程中结合到缺乏骨骼肌的器官中,以及(3)能够诱导多能干细胞形成肌肉。这些假说是先前研究的结果,在这些研究中,来自上胚层和各种缺乏骨骼肌的胎儿器官的少量细胞在体内表达肌源性转录因子MyoD,并在体外分化。对骨骼肌谱系的承诺将通过首先分析调控其他组织发育的转录因子是否与MyoD在上皮细胞中共表达来测试。其次,使用G8抗体从鹌鹑胚胎中分离MyoD阳性的上皮样细胞,移植到发育中的心野区和肢芽的软骨化区,然后分析心脏和软骨特异性分子的表达。为了测试胎儿器官中存在的肌源性干细胞是否来自于外胚层中表达MyoD的细胞,将从鹌鹑外胚层中分离MyoD/G8阳性细胞,将其移植到鸡的外胚层中,发育到胎儿阶段的胚胎,并检查器官中是否存在鹌鹑细胞。成年鸡和小鼠的器官将通过RT-PCR和原位杂交来分析MyoD和Myf5的表达。最后,肌源性干细胞诱导多能干细胞形成肌肉的能力将通过将MyoD/G8阳性细胞与鸡上皮细胞和小鼠胚胎干细胞共同培养来测试。这些实验将开始解决这样一种可能性,即稳定编程的细胞与多能干细胞结合后,可以用来增强体内组织的再生。
英文摘要
DESCRIPTION (provided by applicant): Undifferentiated stem cells are present in the adult organism. In most cases it is unclear whether these cells are capable of differentiating along multiple pathways or programmed to develop along a single pathway. Furthermore, the origin of adult stem cells is unknown. The following studies focus on myogenic stem cells. The general hypotheses to be tested in these experiments are that stem cells committed to the skeletal muscle lineage: (1) are present in the epiblast of the early chick embryo, (2) become incorporated into organs lacking skeletal muscle during gastrulation, and (3) are able to induce multipotent stem cells to form muscle. These hypotheses were formulated as a result of previous studies in which small numbers of cells from the epiblast and a variety of fetal organs lacking skeletal muscle express the myogenic transcription factor MyoD in vivo and differentiate in vitro. Commitment to the skeletal muscle lineage will be tested by first analyzing whether transcription factors that regulate the development of other tissues are co-expressed with MyoD in epiblast cells. Second, MyoD positive epiblast cells will be isolated from the quail embryo using the G8 antibody, implanted into the developing heart fields and chondrogenic region of the limb bud, then analyzed for the expression of cardiac and cartilage specific molecules. To test whether the myogenic stem cells present in fetal organs originate from cells that express MyoD in the epiblast, the MyoD/G8 positive cells will be isolated from the quail epiblast, implanted into the chick epiblast, the embryos grown to fetal stages, and organs examined for the presence of quail cells. Organs from adult chickens and mice will be analyzed by RT-PCR and in situ hybridization for the expression of MyoD and Myf5. Finally, the ability of myogenic stem cells to induce multipotent stem cells to form muscle will be tested by co-culturing MyoD/G8 positive cells with chick epiblast cells and mouse embryonic stem cells. These experiments will begin to address the possibility that stably programmed cells could be used to enhance tissue regeneration in vivo when combined with multipotent stem cells.
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Directing the Fate of Cells to Myogenic Lineages
Directing the Fate of Cells to Myogenic Lineages
Directing the Fate of Cells to Myogenic Lineages
Directing the Fate of Cells to Myogenic Lineages