靶向吲哚胺2,3-双加氧酶1的细胞穿透肽核酸在ifn γ-处理的人角质形成细胞中的抗炎活性

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Biomolecules & Therapeutics Pub Date : 2025-05-01 Epub Date: 2025-04-30 DOI:10.4062/biomolther.2024.207
Daram Jung, Sungjin Ahn, In Guk Park, Yeasel Jeon, Sangbong Lee, Minsoo Noh
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引用次数: 0

摘要

吲哚胺2,3-双加氧酶1 (IDO1)是一种在免疫调节中发挥关键作用的酶,通过代谢色氨酸转化为犬尿氨酸,导致T细胞抑制和促进免疫耐受。然而,IDO1的持续激活可导致皮肤疾病和慢性炎症等炎症条件下的长期免疫刺激。在这项研究中,我们开发了修饰肽核酸(PNAs),结合阳离子脂链靶向IDO1前mrna,并评估了它们在人角质形成细胞中的抗炎作用。修饰的PNAs表现出增强的溶解度,强大的结合亲和力和有效渗透到角质形成细胞。定量PCR结果显示,干扰素γ (IFNγ)处理的角质形成细胞中IDO1和促炎细胞因子如IL-6、IL-8和PTGS2显著下调。这些发现表明,靶向IDO1的细胞穿透PNAs具有治疗炎症性皮肤病和慢性炎症的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Inflammatory Activity of Cell-Penetrating Peptide Nucleic Acids Targeting Indoleamine 2,3-Dioxygenase 1 in IFNγ-Treated Human Keratinocytes.

Indoleamine 2,3-dioxygenase 1 (IDO1) is an enzyme that plays a pivotal role in immune regulation by metabolizing tryptophan into kynurenine, leading to T cell suppression and promoting immune tolerance. However, persistent activation of IDO1 can lead to prolonged immune stimulation in inflammatory conditions such as skin diseases and chronic inflammation. In this study, we developed modified peptide nucleic acids (PNAs) conjugated with cationic lipid chains to target IDO1 pre-mRNA and evaluated their anti-inflammatory effects in human keratinocytes. The modified PNAs demonstrated enhanced solubility, robust binding affinity, and effective penetration into keratinocytes. Quantitative PCR results showed significant downregulation of IDO1 and pro-inflammatory cytokines such as IL-6, IL-8, and PTGS2 in interferon γ (IFNγ)-treated keratinocytes. These findings suggest that cell-penetrating PNAs targeting IDO1 hold potential as a therapeutic approach for inflammatory skin disorders and chronic inflammation.

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来源期刊
CiteScore
6.60
自引率
8.10%
发文量
72
审稿时长
6-12 weeks
期刊介绍: Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.
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