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p38 丝裂原活化蛋白激酶同工型在 12-O-十四烷酰佛波醇 13-乙酸诱导的小鼠皮肤炎症中的作用。

Role of p38 mitogen-activated protein kinase isoforms in murine skin inflammation induced by 12-O-tetradecanoylphorbol 13-acetate.

机构信息

Department of Dermatology, Aarhus University Hospital, Denmark.

出版信息

Acta Derm Venereol. 2011 May;91(3):271-8. doi: 10.2340/00015555-1046.

Abstract

p38 mitogen-activated protein kinase plays a pivotal role in skin inflammation. The purpose of this study was to investigate the role of the various p38 isoforms. p38β/δ-knockout-C57BL/6 mice were generated, studied in a 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced skin inflammation model and compared with wild-type mice. The inflammatory response was determined by ear thickness, myeloperoxidase activity and histology. mRNA and protein expression of interleukin (IL)-1β and IL-6 was determined by quantitative real-time reverse transcription PCR and enzyme-linked immunoassay. In both groups application of TPA resulted in a significant increase in inflammation, and pretreatment with the p38α/β inhibitor, SB202190 resulted in a significant inhibition. A significantly slower onset but prolonged duration of the response was seen in p38β/δ knockout mice. This was paralleled by a significant, but transient, lower IL-1β and IL-6 protein expression in p38β/δ knockout mice. Although the p38α isoform is important, our data also demonstrate an important role of the p38β and/or δ isoforms in the regulation of TPA-induced skin inflammation.

摘要

p38 丝裂原活化蛋白激酶在皮肤炎症中起着关键作用。本研究旨在探讨各种 p38 同工型的作用。生成了 p38β/δ 敲除-C57BL/6 小鼠,在 12-O-十四烷酰佛波醇 13-乙酸酯 (TPA) 诱导的皮肤炎症模型中进行研究,并与野生型小鼠进行比较。通过耳厚度、髓过氧化物酶活性和组织学来确定炎症反应。通过定量实时逆转录 PCR 和酶联免疫吸附试验测定白细胞介素 (IL)-1β 和 IL-6 的 mRNA 和蛋白表达。在两组中,TPA 的应用导致炎症明显增加,并且 p38α/β 抑制剂 SB202190 的预处理导致明显抑制。p38β/δ 敲除小鼠的反应起始明显较慢,但持续时间延长。这与 p38β/δ 敲除小鼠中 IL-1β 和 IL-6 蛋白表达的显著但短暂降低相平行。尽管 p38α 同工型很重要,但我们的数据还表明 p38β 和/或 δ 同工型在调节 TPA 诱导的皮肤炎症中也起着重要作用。

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