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中文摘要
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描述(由申请人提供):NF-kB信号由IkB激酶复合物调节,包括IKK1, IKK2和NEMO。然而,最近的研究表明,IKK1和IKK2在很大程度上具有不同的功能。在这项工作中,我们将确定IKK1在GC B细胞中的内在功能。我们最近报道了表达不能被NIK磷酸化的IKK1突变分子(IKK1AA)的B细胞不形成gc。在这里,我们将通过CD40/BAFF-R/TNF-R2信号传导和T细胞共刺激来检测GC中IKK1依赖的功能,从而确定这一发现的基础。我们还将使用免疫组织化学方法原位评估IKK1通路的激活。为了补充这些研究,将产生表达条件IKK1flox/flox等位基因的小鼠,与诱导的B细胞特异性cre表达小鼠交叉,从而使我们能够在GC反应之前和期间/之后鉴定ikk1依赖的B细胞功能。这些小鼠将与携带突变条件IKK1等位基因的小鼠杂交,以探测IKK1的结构域特异性功能。总之,拟议的研究将提供IKK1在体内功能的明确机制见解。
英文摘要
DESCRIPTION (provided by applicant): NF-kB signaling is regulated by the IkB kinase complex, consisting of IKK1, IKK2 and NEMO. However, recent studies have shown that IKK1 and IKK2 have largely distinct functions. In the proposed work, we will determine the intrinsic functions of IKK1 in GC B cells. We have recently reported that B cells expressing a mutant IKK1 molecule that cannot be phosphorylated by NIK (IKK1AA) do not form GCs. Herein we will determine the basis for this finding by examining IKK1- dependent functions in the GC via CD40/BAFF-R/TNF-R2 signaling and T cell costimulation. We will also assess activation of the IKK1 pathway in situ using immunohistochemical approaches. To complement these studies, mice will be generated expressing conditional IKK1flox/flox alleles to intercross with inducible B cell-specific Cre-expressing mice, thus allowing us to identify IKK1-dependent B cell functions prior to and during/after the GC reaction. These mice will be intercrossed with mice bearing mutant conditional IKK1 alleles to probe domain-specific functions of IKK1. Together, the proposed studies will provide definitive mechanistic insight into IKK1 function in vivo. PUBLIC HEALTH RELEVANCE: Germinal centers are microenvironments that form in the secondary lymphoid tissues following infection or immunization. It is here where B lymphocytes are selected to be high-affinity memory B cells or antibody-producing cells. Thus, understanding the molecular cues that guide germinal center B cell development is critical to understanding the basis of humoral immunity.
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