A20 Mediated Regulation of Colitis and Spondyloarthritis

描述（由申请人提供）：最近的研究表明，炎症性肠病（IBD）是由正常宿主免疫细胞对可引发肠道炎症的微生物分子的反应破坏引起的。树突状细胞（Dendritic cells，DC）是一种对微生物高度敏感的特异性免疫细胞，可以有效激活炎症细胞。由于DC可以频繁地或紧张性地感知肠道中微生物的存在，它们引起炎症的倾向可能取决于它们的细胞内调节或与微生物相遇的“解释”。因此，调节由微生物触发的信号的细胞内蛋白质可能是公开炎症反应的关键。A20是一种酶，有效地限制来自微生物传感途径的信号，包括Toll样受体（TLR），NOD和TNF信号。因此，我们的中心假设是，A20在DC中的特异性表达保持了免疫稳态并预防IBD和IBD相关关节炎。为了验证我们的中心假设，我们已经产生了一种新的小鼠品系，A20 FL/FL CD 11 c-Cre小鼠，其中A20特异性地从DC中缺失。值得注意的是，我们对这些小鼠的初步数据表明，这些小鼠自发地发生结肠炎、血清阴性关节炎和脊椎关节炎，这是人IBD中的典型综合征。我们现在建议使用这些A20 FL/FL CD 11-cre小鼠来确定DC中A20表达与这些挑衅性表型之间的细胞和分子机制。具体而言，我们将确定是否管腔微生物和T细胞参与A20缺陷型DC引起结肠炎和关节炎的病理生理学（目的1）。由于A20可以限制DC中的细胞内信号，包括MyD 88依赖性TLR信号，我们将使用化合物A20 FL/FL MyD 88 FL/FL CD 11 c-Cre小鼠来确定DC中哪些A20调节的信号是MyD 88依赖性的，哪些信号是MyD 88不依赖性的。对这些小鼠的研究将揭示哪些细胞内DC信号和DC产物调节T细胞活化、结肠炎和血清阴性关节炎（Aim 2）。A20是一种泛素修饰酶，可调节信号蛋白的泛素化，也可与NF κ B-1或ABIN-1的A20结合抑制剂结合。为了确定A20和ABIN-1可能协作以限制DC中的信号的分子机制，我们还产生了在DC中特异性缺乏ABIN-1的小鼠。我们现在将使用这些小鼠来研究ABIN-1如何与A20合作以限制DC中的信号传导并预防结肠炎和关节炎（Aim 3）。

DESCRIPTION (provided by applicant): Recent studies suggest that inflammatory bowel disease (IBD) results from the disruption of normal host immune cells responses to microbial molecules that can trigger inflammation in the intestine. Dendritic cells (DCs) are specialized immune cells that are highly sensitive to microbes and can potently activate inflammatory cells. As DCs may frequently or tonically sense the presence of microbes in the intestine, their propensity to cause inflammation may be dependent on their intracellular regulation or "interpretation" of encounters with microbes. Hence, intracellular proteins that regulate signals triggered by microbes may be central to the commitment to overt inflammatory responses. A20 is an enzyme that potently restricts signals from microbial sensing pathways, including Toll-like receptor (TLR), NOD and TNF signals. Thus, our central hypothesis is that A20 expression specifically in DCs preserves immune homeostasis and prevents IBD and IBD-associated arthritis. To test our central hypothesis, we have generated a novel strain of mice, A20FL/FL CD11c-Cre mice, in which A20 is deleted specifically from DCs. Remarkably; our preliminary data with these mice suggest that these mice spontaneously develop colitis, sero-negative arthritis and spondyloarthritis, a stereotypical syndrome in human IBD. We now propose to use these A20FL/FL CD11-cre mice to determine the cellular and molecular mechanisms linking A20 expression in DCs to these provocative phenotypes. Specifically, we will determine whether luminal microbes and T cells are involved in the pathophysiologies by which A20 deficient DCs cause colitis and arthritis (Aim 1). As A20 may restrict intracellular signals in DCs, including MyD88 dependent TLR signals, we will use compound A20FL/FL MyD88FL/FL CD11c-Cre mice to determine which A20 regulated signals in DCs are MyD88-dependent and which signals are MyD88-independent. Studies with these mice will unveil which intracellular DC signals and DC products regulate T cell activation, colitis, and sero-negative arthritis (Aim 2). A20 is a ubiquitn modifying enzyme that regulates ubiquitination of signaling proteins and also binds to A20 Binding Inhibitor of NFkB-1, or ABIN-1. To define the molecular mechanisms by which A20 and ABIN-1 may collaborate to restrict signals in DCs, we have also generated mice lacking ABIN-1 specifically in DCs. We will now use these mice to study how ABIN-1 collaborates with A20 to restrict signaling in DCs and prevent colitis and arthritis (Aim 3).