Expression & function of micro RNAs in neural stem cells

表达

• 批准号: 7229899
• 负责人: MARTIN H GRUMET
• 金额: $ 16.85万
• 依托单位: RUTGERS, THE STATE UNIV OF N.J.
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-01-10 至 2008-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7229899
• 关键词: Adult; Affect; Age; Anatomy; Animals; Brain; Cell Differentiation process; Cells; Characteristics; Class; Condition; Custom; Development; Event; Exploratory/Developmental Grant; Foundations; Gene Targeting; Glial Differentiation; Goals; Guidelines; Human; In Situ Hybridization; In Vitro; Location; Maps; Methods; MicroRNAs; Molecular; Mus; Nervous system structure; Neuroglia; Neurons; Numbers; Pattern; Plants; Program Development; Protein Overexpression; RNA; Radial; Rattus; Regulation; Relative (related person); Reporting; Role; Small Interfering RNA; Solid; Staging; Staining method; Stains; Stem cells; Techniques; Testing; Thinking; Tissues; Transcription Repressor/Corepressor; Translational Repression; Validation; base; cell type; design; in vivo; laser capture microdissection; loss of function; nerve stem cell; neurodevelopment; novel strategies; programs; protein expression; relating to nervous system; transcription factor

DESCRIPTION (provided by applicant): Recent studies have identified a small set of micro RNAs (miRNAs) that are differentially expressed early during CNS development and in cultured stem cells but are lost with differentiation. MiRNAs are thought to act as post-transcriptional repressors of multiple target genes that can regulate protein expression and programs of development. Our hypothesis is that early events in neural development are regulated by specific miRNAs. Thus the restriction of neural stem cells and their progeny to different fates are predicted to be regulated by identifiable sets of miRNAs. Our preliminary results demonstrate that certain sets of miRNAs are expressed transiently in neural stem cells and some of their progeny but are not found in embryoid bodies or adult tissues. We propose two specific aims: (1) Identify miRNAs that are regulated during cortical differentiation. We will determine the relative expression levels of miRNAs during rat and mouse brain development (E10.5-E18.5) by testing miRNAs from different ages on custom-designed miRNA microarrays. Those that are expressed transiently during development or in restricted anatomic locations will then be mapped further by laser capture microdissection to identify discrete pools of cells representing different developmental fates. (2) Modulate differentiation of neural stem cells and radial glia by antisense inhibition or overexpression of specific miRNAs. Gain and loss of function techniques will be used to manipulate miRNA actions in cultured neural stem cells. Two different immortalized clones derived from E13.5 rat cortices that are neurogenic (L2.2) or gliogenic (L2.3) will be used to analyze patterns of neuronal and glial differentiation, respectively. Finally, we will analyze the ability of miRNAs to regulate expression of selected transcription factors that are known to regulate neuronal and glial development. This project represents a novel approach to analyze expression of miRNA during CNS development and to explore how regulation of miRNA expression affects neuronal and glial development.

描述（由申请人提供）：最近的研究已经鉴定了一小组微小RNA（miRNA），其在CNS发育早期和培养的干细胞中差异表达，但随着分化而丢失。miRNAs被认为是多个靶基因的转录后抑制因子，可以调节蛋白质表达和发育程序。我们的假设是，神经发育的早期事件是由特定的miRNA调控的。因此，神经干细胞及其后代对不同命运的限制被预测为受可识别的miRNA组的调节。我们的初步研究结果表明，某些组的miRNAs在神经干细胞和它们的一些后代中瞬时表达，但在胚状体或成体组织中没有发现。我们提出了两个具体的目标：（1）确定在皮质分化过程中调控的miRNA。我们将通过在定制设计的miRNA微阵列上测试来自不同年龄的miRNA来确定大鼠和小鼠大脑发育期间（E10.5-E18.5）miRNA的相对表达水平。那些在发育过程中或在有限的解剖位置短暂表达的细胞将通过激光捕获显微切割进一步映射，以识别代表不同发育命运的离散细胞库。(2)通过反义抑制或过表达特定的miRNA来调节神经干细胞和放射状胶质细胞的分化。功能获得和丧失技术将用于操纵培养的神经干细胞中的miRNA作用。两个不同的永生化克隆衍生自E13.5大鼠皮质，是神经源性（L2.2）或胶质源性（L2.3），将分别用于分析神经元和神经胶质分化的模式。最后，我们将分析miRNAs调节已知调节神经元和神经胶质发育的选定转录因子表达的能力。该项目代表了一种新的方法来分析CNS发育过程中miRNA的表达，并探索miRNA表达的调控如何影响神经元和神经胶质细胞的发育。

项目成果

Differentiating human multipotent mesenchymal stromal cells regulate microRNAs: prediction of microRNA regulation by PDGF during osteogenesis.

• DOI: 10.1016/j.exphem.2008.05.004
• 发表时间: 2008-10
• 期刊: EXPERIMENTAL HEMATOLOGY
• 影响因子: 2.6
• 作者: Goff, Loyal A.;Boucher, Shayne;Ricupero, Christopher L.;Fenstermacher, Sara;Swerdel, Mavis;Chase, Lucas G.;Adams, Christopher C.;Chesnut, Jonathan;Lakshmipathy, Uma;Hart, Ronald P.
• 通讯作者: Hart, Ronald P.