Nrf2 Activation in Keratinocytes: A Central Role in Diabetes-Associated Wound Healing

IF 3.5 3区 医学 Q1 DERMATOLOGY Experimental Dermatology Pub Date : 2024-10-07 DOI:10.1111/exd.15189
Srinivasan Kaussikaa, Murali Krishna Prasad, Kunka Mohanram Ramkumar
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Abstract

Wound healing is a complex biological process crucial for tissue repair, wherein keratinocytes play a pivotal role in initiating, sustaining and completing the cascade. Various local and systemic factors, such as lifestyle, age metabolic disorders and vascular insufficiency, can influence this process, and in the context of diabetic wounds, disrupted biological mechanisms, including inflammation, tissue hypoxia, decrease in collagen production along with increased oxidative stress and keratinocyte dysfunction, contribute to delayed healing. During re-epithelialisation, keratinocytes undergo rapid multiplication and migration, forming a dense hyperproliferative epithelial layer that restores the epidermal barrier. Nuclear factor-erythroid 2-related factor (Nrf2), a vital transcription factor, emerges as a central regulator in managing antioxidant proteins and detoxifying enzymes, serving as a guardian against elevated reactive oxygen species (ROS) levels during stress. Nrf2 also orchestrates angiogenesis and anti-inflammatory responses crucial for wound repair. Studies demonstrate that under high-glucose conditions, Nrf2 activation promotes wound healing by enhancing cell proliferation and migration while reducing apoptosis. Nrf2 activators stimulate endogenous antioxidant production, thereby mitigating oxidative stress. Furthermore, Nrf2 upregulation is associated with decreased expression of cytokines such as TNF-α and IL- 6. Recent research underscores the potential of bioactive molecules, including dietary polyphenols, traditional medicinal compounds and pharmacological agents, in activating Nrf2 and preventing diseases such as diabetes due to their robust antioxidative properties. This review aims to investigate the activation of Nrf2 by these bioactive molecules in cultured keratinocytes and animal models, elucidating the key molecular regulatory mechanisms involved in alleviating oxidative stress and facilitating the diabetic wound healing process. Understanding these complex pathways may offer insights into novel therapeutic strategies for enhanced wound healing in diabetes-associated complications.

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角质形成细胞中的 Nrf2 激活:在糖尿病相关伤口愈合中的核心作用
伤口愈合是一个复杂的生物过程,对组织修复至关重要,其中角质细胞在启动、维持和完成级联过程中发挥着关键作用。各种局部和全身因素,如生活方式、年龄、代谢紊乱和血管功能不全等,都会影响这一过程,而在糖尿病伤口中,生物机制紊乱,包括炎症、组织缺氧、胶原蛋白生成减少、氧化应激增加和角质形成细胞功能障碍等,都会导致伤口愈合延迟。在表皮重建过程中,角质形成细胞会迅速增殖和迁移,形成致密的增生上皮层,从而恢复表皮屏障。核因子-红细胞 2 相关因子(Nrf2)是一种重要的转录因子,它是管理抗氧化蛋白和解毒酶的核心调节因子,在应激过程中起到保护作用,防止活性氧(ROS)水平升高。Nrf2 还能协调对伤口修复至关重要的血管生成和抗炎反应。研究表明,在高血糖条件下,Nrf2 的活化可促进细胞增殖和迁移,同时减少细胞凋亡,从而促进伤口愈合。Nrf2 激活剂可刺激内源性抗氧化剂的产生,从而减轻氧化应激。此外,Nrf2 的上调与 TNF-α 和 IL- 6 等细胞因子的表达减少有关。最近的研究强调了生物活性分子(包括膳食多酚、传统药用化合物和药剂)在激活 Nrf2 和预防糖尿病等疾病方面的潜力,因为它们具有强大的抗氧化特性。本综述旨在研究这些生物活性分子在培养的角质细胞和动物模型中对 Nrf2 的激活作用,阐明参与缓解氧化应激和促进糖尿病伤口愈合过程的关键分子调控机制。了解这些复杂的通路可为制定新的治疗策略提供见解,从而促进糖尿病相关并发症的伤口愈合。
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来源期刊
Experimental Dermatology
Experimental Dermatology 医学-皮肤病学
CiteScore
6.70
自引率
5.60%
发文量
201
审稿时长
2 months
期刊介绍: Experimental Dermatology provides a vehicle for the rapid publication of innovative and definitive reports, letters to the editor and review articles covering all aspects of experimental dermatology. Preference is given to papers of immediate importance to other investigators, either by virtue of their new methodology, experimental data or new ideas. The essential criteria for publication are clarity, experimental soundness and novelty. Letters to the editor related to published reports may also be accepted, provided that they are short and scientifically relevant to the reports mentioned, in order to provide a continuing forum for discussion. Review articles represent a state-of-the-art overview and are invited by the editors.
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