Regulation of Foxp3 Function

Foxp3功能的调控

基本信息

批准号：
8206600
负责人：
ANDREW D WELLS
金额：
$ 36.28万
依托单位：
CHILDREN'S HOSP OF PHILADELPHIA
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-01-15 至 2013-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8206600
关键词：
Autoimmune Diseases Binding CD4 Positive T Lymphocytes CD8B1 gene Carcinoma Cell physiology Cells Cytokine Gene DNA Binding DNA-Binding Proteins Diabetes Mellitus Experimental Models Family Gene Expression Gene Targeting Genetic Programming Genetic Transcription Graft Rejection Human Human Resources IL2 gene IL2RA gene IL4 gene Immune Immune Tolerance Inflammatory Interferons Interleukin-10 Interleukin-2 Jurkat Cells Laboratories Mediating Modeling Molecular Mus Mutation Names Organ Transplantation Participant Pathology Principal Investigator Publishing Regulation Regulatory T-Lymphocyte Reporter Repression Research Research Personnel Retroviral Vector Structure T-Lymphocyte Techniques Thymus Gland allograft rejection design experience gene induction improved member mutant novel therapeutics programs promoter research study

项目摘要

DESCRIPTION (provided by applicant): Regulatory T cells are crucial for the control of immune-mediated pathology during organ transplant rejection and autoimmune disease, therefore understanding the underlying mechanisms by which these cells function will be critical for promoting immune tolerance in humans. Recent studies in experimental models have established that Foxp3, which is a member of the forkhead family of DNA binding proteins, is necessary and sufficient for specification of regulatory T lymphocyte lineage choice and function. and therefore is crucial for acquired immune tolerance. Expression of Foxp3 initiates a unique transcriptional program which includes the induction of genes such as GITR, CD25, CTLA-4, IL-10 and TGF2, and repression of pro-inflammatory cytokine genes such as IL-2 and IFN?. The mechanisms by which Foxp3 enforces this genetic program are unclear. The studies proposed in this application are centered around basic questions of how Foxp3 binds to target genes, and how Foxp3 represses or induces transcription at these loci. The proposed studies will add significantly to our understanding of how Foxp3 regulates gene expression, and the information gained from these studies will have relevance for the design of novel therapeutic strategies by which tolerance can be promoted in humans.

描述（由申请人提供）：调节性 T 细胞对于器官移植排斥和自身免疫性疾病期间免疫介导的病理学的控制至关重要，因此了解这些细胞发挥作用的潜在机制对于促进人类免疫耐受至关重要。最近的实验模型研究表明，Foxp3（DNA 结合蛋白叉头家族的成员）对于调节性 T 淋巴细胞谱系选择和功能的规范是必要且充分的。因此对于获得性免疫耐受至关重要。 Foxp3的表达启动独特的转录程序，包括诱导GITR、CD25、CTLA-4、IL-10和TGF2等基因，以及抑制促炎细胞因子基因（例如IL-2和IFNα）。 Foxp3 执行该遗传程序的机制尚不清楚。本申请中提出的研究主要围绕 Foxp3 如何与靶基因结合以及 Foxp3 如何抑制或诱导这些基因座的转录的基本问题。拟议的研究将显着增加我们对 Foxp3 如何调节基因表达的理解，并且从这些研究中获得的信息将与设计新的治疗策略相关，通过该策略可以促进人类的耐受性。

项目成果

期刊论文数量（3）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

A ChIP-seq-defined genome-wide map of MEF2C binding reveals inflammatory pathways associated with its role in bone density determination.

ChIP-seq 定义的 MEF2C 结合全基因组图谱揭示了与其在骨密度测定中的作用相关的炎症途径。

DOI：
发表时间：
2014-04
期刊：
影响因子：
4.2
作者：
Johnson, Matthew E;Deliard, Sandra;Zhu, Fengchang;Xia, Qianghua;Wells, Andrew D;Hankenson, Kurt D;Grant, Struan F A
通讯作者：
Grant, Struan F A

Mutiny on the Boun-T: controlling dangerous T cells through anergy.

Boun-T 上的叛变：通过无能控制危险的 T 细胞。