Initiation of the Sterile Inflammatory Response in Acute Pancreatitis

急性胰腺炎无菌炎症反应的启动

• 批准号: 8496030
• 负责人: Rafaz Hoque
• 金额: $ 15.48万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-15 至 2016-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8496030
• 关键词: Acinar Cell; Alcohol consumption; Binding; Bone Marrow; Caerulein; Caspase-1; Cell Communication; Cell Death; Cells; Chimera organism; Cholelithiasis; Coculture Techniques; DNA; Data; Disease; Edema; Enzyme Precursors; Immune; Individual; Inflammation; Inflammatory Response; Injury; Interleukin-18; Interleukins; Leucocytic infiltrate; Life; Link; Molecular; NADP; Pancreas; Pancreatic Injury; Pancreatic duct; Pancreatitis; Pathway interactions; Pattern; Pharmaceutical Preparations; Population; Process; Production; Proteins; Regulation; Relative (related person); Role; Signal Transduction; Sterility; TLR4 gene; Therapeutic; Up-Regulation; Work; acute pancreatitis; cell injury; cytotoxicity; design; effective therapy; in vivo; inhibitor/antagonist; injured; neutrophil; prevent; receptor; research study; response

DESCRIPTION (provided by applicant): Acute pancreatitis (AP) is initiated by injury to pancreatic acinar cells resulting in zymogen activation. This initial insult induces a rapid sterile inflammatory response (SIR) characterized by edema, cellular infiltrate, and further acinar cell death. Many lines of evidence point towards the SIR having a vital role in pancreatic damage, but the crucial link between acinar cell injury and induction of the SIR has not been identified. Our preliminary data demonstrate that in caerulein-induced acute pancreatitis: i. In the absence of TLR9 or the inflammasome components ASC, NLRP3, and caspase-1 there is reduced SIR and acinar cell injury. ii. Inhibitors of TLR9 can reduce the SIR and acinar cell death. iii. TLR9 expression is localized to resident immune, endothelial, and pancreatic duct cells in vivo. We hypothesize that initial acinar cell injury releases damage associated molecular patterns (DAMPs) which are sensed by resident pancreatic cells, resulting in the SIR which increases acinar cell death. Aim 1: Identify the pancreatic DAMP-sensing cell. (a) Bone marrow chimeras will be constructed to identify the relative contribution of immune and parenchymal cells to the SIR. (b) Selective depletion will determine the contributions of individual cell populations to the SIR. Aim 2: Identify which components of inflammasome activation induce acinar cell cytotoxicity. Acinar cells will be isolated and assessed for cell death and zymogen activation in response to (a) IL-1beta and IL-18, and (b) co-culture with the DAMP-sensing cell identified in Aim 1. Aim 3: Identify the regulation of the inflammasome and TLR9 signaling by TLR4 activation in acute pancreatitis. The ability of TLR4 activation to regulate both (a) NLRP3 inflammasome and (b) TLR9 signaling will be assessed in the DAMP-sensing cells identified in Aim 1. The proposed work will identify a detailed cellular and molecular mechanism for the initiation of the inflammatory response in acute pancreatitis.

描述（由申请人提供）：急性胰腺炎（AP）是由胰腺腺泡细胞损伤导致酶原激活引起的。这种最初的损伤诱导快速无菌炎症反应（SIR），其特征是水肿、细胞浸润和进一步的腺泡细胞死亡。许多证据表明SIR在胰腺损伤中起着至关重要的作用，但腺泡细胞损伤与SIR诱导之间的关键联系尚未确定。我们的初步数据表明，在小蛋白诱导的急性胰腺炎中：i.在缺乏TLR9或炎性小体成分ASC、NLRP3和caspase-1的情况下，SIR和腺泡细胞损伤减少。2。TLR9抑制剂可降低SIR和腺泡细胞死亡。3。在体内，TLR9的表达局限于常驻免疫细胞、内皮细胞和胰管细胞。我们假设最初的腺泡细胞损伤释放损伤相关分子模式（DAMPs），这些损伤相关分子模式被常驻胰腺细胞感知，导致SIR增加腺泡细胞死亡。目的1：鉴定胰腺湿感细胞。(a)将构建骨髓嵌合体，以确定免疫细胞和实质细胞对SIR的相对贡献。(b)选择性耗竭将决定单个细胞群对SIR的贡献。目的2：确定炎性小体激活的哪些成分诱导腺泡细胞毒性。将分离腺泡细胞并评估细胞死亡和酶原激活情况，以响应(a) il -1 β和IL-18，以及(b)与Aim 1中鉴定的潮湿感应细胞共培养。目的3：研究急性胰腺炎中TLR4激活对炎性小体和TLR9信号的调控。TLR4激活调节(a) NLRP3炎性体和(b) TLR9信号传导的能力将在Aim 1中鉴定的damp传感细胞中进行评估。提出的工作将确定一个详细的细胞和分子机制的启动炎症反应在急性胰腺炎。