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The Role of Necroptosis, Apoptosis, and Inflammation in Fowl Cholera-Associated Liver Injury in a Chicken Model

机译:Necroptis,细胞凋亡和炎症在鸡模型中禽霍乱相关肝损伤的作用

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Fowl cholera resulting from infection with Pasteurella multocida causes huge economic losses in the poultry industry. Necrotic hepatitis is reported to be a significant lesion associated with fowl cholera in chickens. Clarifying the underlying molecular mechanism of hepatic injury caused by P. multocida infection is needed to develop new strategies to control fowl cholera. Pasteurella multocida Q (the standard reference strain) and P. multocida 1G1 (a clinical strain) were used to infect healthy laying hens. Clinical signs were observed and gross lesions in livers were observed postmortem. Histologic lesions and the localization and expression of protein molecules associated with necroptosis, apoptosis, and inflammation in hepatic tissues were examined by hematoxylin and eosin staining and immunohistochemistry. Western blot analysis was used to determine the expression of liver injury-related genes. Necroptotic molecules such as RIPK1 (receptor interaction protein kinases 1), RIPK3 (receptor interaction protein kinases 3), and MLKL (mixed lineage kinase domain-like protein) were observed by immunostaining primarily in the cytoplasm of hepatocytes within or around necrotic foci, and inflammatory mediators HMGB1 (high-mobility group box 1) and IL-6 (interleukin-6) were found in the cytoplasm of heterophils, monocytes/ macrophages, and hepatic sinusoids. In addition, MMP9 (matrix metalloproteinase 9) and TIMP1 (tissue inhibitor of metalloproteinase 1) were observed in hepatic parenchymal cells, inflammatory cells, and interstitial spaces, whereas the apoptotic effector molecule caspase-3 (cysteine-containing aspartic proteolytic enzymes 3) was mainly found in hepatocytes. The expression of RIPK1, RIPK3, and MLKL was significantly higher in the infected chickens than in the controls. HMGB1 and IL-6 protein levels were also increased in infected chickens relative to those in controls. Both MMP9 and TIMP1 were highly expressed in infected chickens. In addition, caspase-3 protein levels were significantly elevated in infected chickens. Necroptosis, apoptosis, and inflammation played a significant role in hepatic injury caused by P. multocida.
机译:由Pasteurella Multocad感染引起的禽霍乱导致家禽业的经济损失巨大。据报道,坏死性肝炎是鸡中鸡霍乱相关的重要病变。阐明P. Multocida感染引起的肝损伤的潜在分子机制,以产生控制禽霍乱的新策略。 Pasteurella Multiocida Q(标准参考菌株)和P. Multocida 1G1(临床菌株)用于感染健康的母鸡。观察到临床迹象,并观察到肝脏的严重病变被观察到淘汰后期。通过苏木精和曙红染色和免疫组化检查肝脏组织中患者凋亡,细胞凋亡和肝脏组织相关蛋白质分子的组织病变和蛋白质分子的局部化和表达。 Western印迹分析用于确定肝损伤相关基因的表达。通过主要染色在坏死病灶内或周围的肝细胞的细胞质中,通过免疫染色,观察诸如RIPK1(受体相互作用蛋白激酶1),RIPK3(受体相互作用蛋白激酶1),RIPK3(受体相互作用蛋白激酶3)和MLK1(混合谱系激酶畴样蛋白),在异质,单核细胞/巨噬细胞和肝脏正弦状细胞质中发现炎症介质HMGB1(高迁移率组箱1)和IL-6(白细胞介素-6)。另外,在肝实质细胞,炎症细胞和间质空间中观察MMP9(基质金属蛋白酶9)和TIMP1(金属蛋白酶1的组织抑制剂),而凋亡效应分子Caspase-3(含半胱氨酸天冬氨酸蛋白化酶3)是主要在肝细胞中发现。感染鸡的表达显着高于对照物。在感染的鸡中相对于对照中的那些,HMGB1和IL-6蛋白水平也增加。 MMP9和TIMP1两者都在受感染的鸡中表达。此外,Caspase-3蛋白水平在受感染的鸡中显着升高。 Necroptis,细胞凋亡和炎症在P. Multocida引起的肝损伤中发挥了重要作用。

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