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Stem Cell Microvesicles: Potential Tools for Retinal Regeneration

干细胞微泡：视网膜再生的潜在工具

基本信息

批准号：
7534779
负责人：
DEBORA B FARBER
金额：
$ 19.25万
依托单位：
UNIVERSITY OF CALIFORNIA LOS ANGELES
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-12-01 至 2009-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7534779
关键词：
Anterior Aqueous Humor Blood Platelets Bromodeoxyuridine Cell Culture Techniques Cell membrane Cells Ciliary Body Complex Cues EGF gene ES Cell Line Electron Microscopy Endothelial Cells Environment Epithelium Eye FGF2 gene Goals Green Fluorescent Proteins Hematopoietic Human Immunohistochemistry In Vitro Injection of therapeutic agent Invertebrates Label Lead Learning Lipids Liquid Chromatography Lymphocyte Mammals Mass Spectrum Analysis Mediating Mediator of activation protein Membrane Proteins Messenger RNA MicroRNAs Microarray Analysis Molecular Multipotent Stem Cells Mus Natural regeneration Play Population Proteins RNA Reporting Retina Retinal Reverse Transcriptase Polymerase Chain Reaction Role Signal Transduction Small RNA Stem cell transplant Stem cells Supporting Cell Testing Time Transcript Transfer RNA Translations Vertebrates Vesicle Western Blotting anterior chamber aqueous cell type embryonic stem cell extracellular granulocyte immunocytochemistry in vivo intercellular communication migration nano neoplastic cell nestin protein novel paracrine particle pluripotency progenitor programs protein profiling regenerative research study retinal progenitor cell retinal regeneration stem stem cell differentiation stem cell fate stem cell niche stem cell population tool

项目摘要

DESCRIPTION (provided by applicant): The retina in lower vertebrates shows a remarkable regenerative ability that is lost in mammals. Multipotent progenitor cells, that are capable of differentiating into a variety of retinal cell types, have been isolated from the ciliary margin and retina of mammalian eyes. Despite their presence, these progenitor cells are normally quiescent and unable to regenerate damaged retina. This proposal will investigate the ability of microvesicles, released from mouse embryonic stem cells, to reactivate mouse retinal progenitor cells. The long term goal of this project is to discover novel ways of reactivating quiescent progenitor cell populations in the human eye, so that regeneration of damaged retina may be possible. Microvesicles are plasma-membrane particles that are released into the extracellular environment. Very recently, microvesicles have been reported from embryonic stem cells cultured in vitro. Our preliminary results show that these embryonic stem cell microvesicles contain RNA and protein. Most interestingly, they contain a specific class of RNA molecules called microRNAs, which are potent regulators of translation. Microvesicles may serve a role in intercellular communication in one of several manners. They may transfer microRNAs, mRNAs, or proteins to cells. Alternatively they can signal cells through surface proteins found on microvesicles. Our first aim is to characterize the RNA and protein contents of mouse embryonic stem cell microvesicles to look for candidates that might alter stem cell programming. We will use microarray analysis and qRT-PCR for mRNA and microRNA profiling, and mass spectrometry, Western blot analysis, and immunocytochemistry for protein profiling. We will also explore in Aim I the ability of these microvesicles to directly transfer RNA or protein to cells in vitro. Our second aim is to determine if these microvesicles can activate the quiescent stem cell population found in the ciliary margin and retina of mouse eyes. We will inject microvesicles into the aqueous, vitreous, and subretinal space of mice and look for increased proliferation of stem cells with BrDU- labeling. Our final aim is to look for endogenous microvesicles in the aqueous and vitreous and also to characterize them using microarray profiling, qRT-PCR, mass spectrometry, Western blot analysis, immunocytochemistry, and electron microscopy. The information generated in this proposal will not only lead to an increased understanding of the role that extrinsic mRNA, microRNAs, and proteins play in determining stem cell fate, but may also identify microvesicles as novel endogenous signaling factors in the eye, and possibly contributing to the stem cell niche.

描述（由申请人提供）：低等脊椎动物的视网膜显示出在哺乳动物中丧失的显著的再生能力。多能祖细胞，能够分化成各种视网膜细胞类型，已经从哺乳动物眼睛的睫状缘和视网膜分离。尽管它们的存在，这些祖细胞通常是静止的，不能再生受损的视网膜。这项提议将研究从小鼠胚胎干细胞释放的微泡重新激活小鼠视网膜祖细胞的能力。该项目的长期目标是发现重新激活人眼中静止祖细胞群的新方法，从而使受损视网膜的再生成为可能。微泡是释放到细胞外环境中的质膜颗粒。最近，已经报道了来自体外培养的胚胎干细胞的微泡。我们的初步结果表明，这些胚胎干细胞微泡含有RNA和蛋白质。最有趣的是，它们含有一类特殊的RNA分子，称为microRNA，这是翻译的有效调节因子。微泡可以以几种方式之一在细胞间通讯中起作用。它们可以将microRNA、mRNA或蛋白质转移到细胞中。或者，它们可以通过在微泡上发现的表面蛋白质向细胞发出信号。我们的第一个目标是表征小鼠胚胎干细胞微泡的RNA和蛋白质含量，以寻找可能改变干细胞编程的候选者。我们将使用微阵列分析和qRT-PCR进行mRNA和microRNA分析，并使用质谱法、Western印迹分析和免疫细胞化学进行蛋白质分析。我们还将在Aim I中探索这些微泡在体外直接将RNA或蛋白质转移到细胞中的能力。我们的第二个目标是确定这些微泡是否可以激活小鼠眼睛睫状缘和视网膜中发现的静止干细胞群。我们将微泡注射到小鼠的房水、玻璃体和视网膜下腔中，并寻找BrDU标记的干细胞增殖增加。我们的最终目的是寻找内源性微泡在水和玻璃体，并使用微阵列分析，qRT-PCR，质谱，Western印迹分析，免疫细胞化学和电子显微镜来表征它们。在这个提议中产生的信息不仅会导致增加对外源性mRNA，microRNA和蛋白质在决定干细胞命运中所起作用的理解，而且还可能将微泡确定为眼睛中的新型内源性信号传导因子，并可能有助于干细胞生态位。