FACTORS AND GENES RESPONSIBLE FOR ADIPOCYTE COMMITMENT
影响脂肪细胞承诺的因素和基因
基本信息
- 批准号:6916180
- 负责人:
- 金额:$ 40.88万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2003
- 资助国家:美国
- 起止时间:2003-09-15 至 2007-08-31
- 项目状态:已结题
- 来源:
- 关键词:SDS polyacrylamide gel electrophoresisadipocytesadipose tissueathymic mousebone morphogenetic proteinsgene expressionimmunocytochemistryliquid chromatographymass spectrometrymessenger RNAnorthern blottingsphosphorylationpolymerase chain reactionposttranslational modificationsprotein structure functionstem cellstissue /cell culturetransfectionwestern blottings
项目摘要
DESCRIPTION: The long-term goal is to determine the mechanisms by which pluripotent stem cells of the vascular stroma of adipose tissue undergo commitment to the adipocyte lineage. The SPECIFIC AIMS are: 1. (A) To identify BMP4-induced genes and proteins, and (B) to identify molecules that undergo phosphorylation on serine, threonine or tyrosine residues upon BMP4 treatment in C3H10TI/2 pluripotent stem cells. 2. To determine whether expression of genes "identified" above causes commitment to the adipocyte lineage in cell culture or in vivo contexts and to determine the mechanistic basis for such commitment. 3. To identify, using a proteomic approach, secreted proteins that initiate, or are involved in, the commitment process.
Changes in gene expression induced by BMP4 will be examined at both the mRNA transcript and protein levels. At the transcript level, changes in expression will be monitored with oligonucleotide arrays. Since mRNA and protein levels do not always reflect regulation by post-transcriptional mechanisms, differences in protein levels will also be directly assessed by mass spectrometry-based proteomic methods. This combined approach should not only provide verification of the transcript data, but also allow identification of molecules whose mRNA levels do not change and would otherwise be missed by microarray-based methods. Other advantages of mass spectrometry-based methods include identification of proteins that undergo post-translational modifications such as BMP4-induced phosphorylation and identification of novel molecules by de novo sequencing.
Our studies should result in a detailed map of the adipocyte commitment process, as we should not only be able to identify the extracellular factors that influence this process but also elucidate the intracellular signaling pathways that are involved.
描述:长期目标是确定脂肪组织血管间质多能干细胞向脂肪细胞谱系转变的机制。具体目标是:1。(A)鉴定BMP4诱导的基因和蛋白,(B)鉴定在C3H10TI/2多能干细胞中BMP4处理后丝氨酸、苏氨酸或酪氨酸残基磷酸化的分子。2. 确定上述“鉴定”的基因的表达是否在细胞培养或体内环境下导致脂肪细胞系的承诺,并确定这种承诺的机制基础。3. 用蛋白质组学方法鉴定启动或参与承诺过程的分泌蛋白。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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M DANIEL LANE其他文献
M DANIEL LANE的其他文献
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{{ truncateString('M DANIEL LANE', 18)}}的其他基金
FACTORS AND GENES RESPONSIBLE FOR ADIPOCYTE COMMITMENT
影响脂肪细胞承诺的因素和基因
- 批准号:
6730265 - 财政年份:2003
- 资助金额:
$ 40.88万 - 项目类别:
FACTORS AND GENES RESPONSIBLE FOR ADIPOCYTE COMMITMENT
影响脂肪细胞承诺的因素和基因
- 批准号:
6799692 - 财政年份:2003
- 资助金额:
$ 40.88万 - 项目类别:
FACTORS AND GENES RESPONSIBLE FOR ADIPOCYTE COMMITMENT
影响脂肪细胞承诺的因素和基因
- 批准号:
7098681 - 财政年份:2003
- 资助金额:
$ 40.88万 - 项目类别:
Antiadipogenic Influence of HIV Protease Inhibitors
HIV 蛋白酶抑制剂的抗脂肪形成作用
- 批准号:
6423684 - 财政年份:2002
- 资助金额:
$ 40.88万 - 项目类别:
Antiadipogenic Influence of HIV Protease Inhibitors
HIV 蛋白酶抑制剂的抗脂肪形成作用
- 批准号:
6620938 - 财政年份:2002
- 资助金额:
$ 40.88万 - 项目类别:
Antiadipogenic Influence of HIV Protease Inhibitors
HIV 蛋白酶抑制剂的抗脂肪形成作用
- 批准号:
6700257 - 财政年份:2002
- 资助金额:
$ 40.88万 - 项目类别:
Antiadipogenic Influence of HIV Protease Inhibitors
HIV 蛋白酶抑制剂的抗脂肪形成作用
- 批准号:
6848325 - 财政年份:2002
- 资助金额:
$ 40.88万 - 项目类别:
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