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深入了解银屑病中的腺苷途径:阐明其作用和潜在的治疗应用。

Insight into adenosine pathway in psoriasis: Elucidating its role and the potential therapeutical applications.

机构信息

Department of Pharmacy, University of Salerno, Fisciano, SA, Italy; PhD Program in Drug Discovery and Development, University of Salerno, Fisciano, SA, Italy.

Department of Pharmacy, University of Naples "Federico II", Napoli, NA, Italy; PhD Program in Nutraceuticals, Functional Foods and Human Health, University of Naples "Federico II", Napoli, NA, Italy.

出版信息

Life Sci. 2024 Nov 15;357:123071. doi: 10.1016/j.lfs.2024.123071. Epub 2024 Sep 21.

Abstract

Psoriasis is an inflammatory skin disease, that can manifest as different phenotypes, however its most common form is psoriasis vulgaris (plaque psoriasis), characterized by abnormal keratinocyte proliferation, leading to characteristic histopathological signs of acanthosis, hyperkeratosis and parakeratosis. For many years, there has been a debate regarding whether keratinocyte dysfunction leads to immune system dysregulation in psoriasis or vice versa. It is now understood that epidermal hyperplasia results from immune system activation. Besides epidermal hyperplasia, psoriatic skin shows leukocyte infiltration, evident angiogenesis in the papillary dermis, characterized by tortuous, dilated capillaries, as well as oedema. There is substantial early evidence that adenosine is a key mediator of the immune response; it derives from ATP hydrolysis and accumulates into tissue in response to systemic and local stress conditions, hypoxia, metabolic stress, inflammation. Adenosine controls several cell functions by signalling through its 4 receptor subtypes, A, A, A and A. Evidence suggests that adenosine may play a role in psoriasis pathogenesis by controlling several immune cell functions, keratinocyte proliferation, neo-angiogenesis. Expression of adenosine receptor varies in psoriatic skin, and this can significantly impact on tissue homeostasis. Indeed, an altered adenosine receptor profile may contribute to the dysregulation observed in psoriasis, affecting immune responses and inflammatory pathways. Here, we discuss the role of adenosine in regulating the functions of the main cell populations implied in the pathogenesis of psoriasis. Furthermore, we give evidence for adenosine signalling pathway as target for therapeutic intervention in psoriasis.

摘要

银屑病是一种炎症性皮肤病,可以表现为不同的表型,但最常见的形式是寻常型银屑病(斑块状银屑病),其特征是角质形成细胞异常增殖,导致棘层肥厚、角化过度和角化不全等特征性组织病理学表现。多年来,人们一直在争论是角质形成细胞功能障碍导致银屑病的免疫系统失调,还是反之亦然。现在人们已经明白,表皮增生是免疫系统激活的结果。除了表皮增生,银屑病皮肤还表现为白细胞浸润,乳头层明显的血管生成,表现为扭曲、扩张的毛细血管以及水肿。有大量早期证据表明,腺苷是免疫反应的关键介质;它来自于 ATP 的水解,并在全身和局部应激条件、缺氧、代谢应激、炎症反应时积聚到组织中。腺苷通过其 4 种受体亚型 A、A、A 和 A 传递信号,控制着几种细胞功能。有证据表明,腺苷可能通过控制几种免疫细胞功能、角质形成细胞增殖和新血管生成,在银屑病发病机制中发挥作用。在银屑病皮肤中,腺苷受体的表达存在差异,这可能对组织稳态产生重大影响。事实上,腺苷受体谱的改变可能导致银屑病中观察到的失调,影响免疫反应和炎症途径。在这里,我们讨论了腺苷在调节参与银屑病发病机制的主要细胞群的功能中的作用。此外,我们还提供了腺苷信号通路作为银屑病治疗干预靶点的证据。

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