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首页> 外文期刊>The Journal of investigative dermatology. >Topical ROR Inverse Agonists Suppress Inflammation in Mouse Models of Atopic Dermatitis and Acute Irritant Dermatitis
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Topical ROR Inverse Agonists Suppress Inflammation in Mouse Models of Atopic Dermatitis and Acute Irritant Dermatitis

机译:局部ROR反向激动剂抑制特应性皮炎和急性刺激性皮炎的小鼠模型中的炎症

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摘要

The retinoic acid receptor-related orphan receptors RORα and RORγ are critical for the functions of specific subsets of T cells and innate lymphoid cells, which are key drivers of inflammatory disease in barrier tissues. Here, we investigate the anti-inflammatory potential of SR1001, a synthetic RORα/γ inverse agonist, in mouse models of atopic dermatitis and acute irritant dermatitis. Topical treatment with SR1001 reduces epidermal and dermal features of MC903-induced atopic dermatitis-like disease and suppresses the production of type 2 cytokines and other inflammatory mediators in lesional skin. In the epidermis, SR1001 treatment blocks MC903-induced expression of TSLP and reverses impaired keratinocyte differentiation. SR1001 is also effective in alleviating acute dermatitis triggered by 12- O -tetradecanoylphorbol-13-acetate. Overall, our results suggest that RORα/γ are important therapeutic targets for cutaneous inflammation and suggest topical usage of inhibitory ligands as an approach to treating skin diseases of inflammatory etiology.
机译:视黄酸受体相关的孤儿受体RORα和RORγ是用于T细胞和先天淋巴样细胞的特定子集的功能,这些功能是在阻挡组织炎性疾病的关键因素是至关重要的。在这里,我们调查SR1001,合成RORα/γ反相激动剂的抗炎潜力,在小鼠模型的过敏性皮炎和急性刺激性皮炎。与SR1001局部治疗降低MC903诱导的异位性的表皮和真皮特征皮炎样疾病并抑制生产2型细胞因子和在损伤皮肤等炎症介质的。在表皮,SR1001处理块MC903诱导的TSLP的表达和挫折受损角质形成细胞分化。 SR1001是也有效地缓解急性性皮炎12-ö-tetradecanoylphorbol -13-乙酸酯触发。总的来说,我们的研究结果表明,RORα/γ对于皮肤炎症重要的治疗目标,并提出抑制性配体局部使用作为一种方法来治疗炎症的病因的皮肤疾病。

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