Promoting Articular Cartilage Regeneration through Microenvironmental Regulation.

IF 3.5 3区 医学 Q2 IMMUNOLOGY Journal of Immunology Research Pub Date : 2024-07-26 eCollection Date: 2024-01-01 DOI:10.1155/2024/4751168
Kai Liu, Bingjun Zhang, Xiaoling Zhang
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Abstract

In recent years, as the aging population continues to grow, osteoarthritis (OA) has emerged as a leading cause of disability, with its incidence rising annually. Current treatments of OA include exercise and medications in the early stages and total joint replacement in the late stages. These approaches only relieve pain and reduce inflammation; however, they have significant side effects and high costs. Therefore, there is an urgent need to identify effective treatment methods that can delay the pathological progression of this condition. The changes in the articular cartilage microenvironment, which are complex and diverse, can aggravate the pathological progression into a vicious cycle, inhibiting the repair and regeneration of articular cartilage. Understanding these intricate changes in the microenvironment is crucial for devising effective treatment modalities. By searching relevant research articles and clinical trials in PubMed according to the keywords of articular cartilage, microenvironment, OA, mechanical force, hypoxia, cytokine, and cell senescence. This study first summarizes the factors affecting articular cartilage regeneration, then proposes corresponding treatment strategies, and finally points out the future research direction. We find that regulating the opening of mechanosensitive ion channels, regulating the expression of HIF-1, delivering growth factors, and clearing senescent cells can promote the formation of articular cartilage regeneration microenvironment. This study provides a new idea for the treatment of OA in the future, which can promote the regeneration of articular cartilage through the regulation of the microenvironment so as to achieve the purpose of treating OA.

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通过微环境调节促进关节软骨再生
近年来,随着老龄人口的不断增长,骨关节炎(OA)已成为导致残疾的主要原因,其发病率逐年上升。目前治疗 OA 的方法包括早期的运动和药物治疗,以及晚期的全关节置换。这些方法只能缓解疼痛和减轻炎症,但副作用大、费用高。因此,迫切需要找到有效的治疗方法,以延缓这一病症的病理发展。关节软骨微环境的变化复杂多样,会加剧病理进展,形成恶性循环,抑制关节软骨的修复和再生。了解微环境中这些错综复杂的变化对于设计有效的治疗方法至关重要。本研究以关节软骨、微环境、OA、机械力、缺氧、细胞因子和细胞衰老为关键词,在PubMed上搜索相关研究文章和临床试验。本研究首先总结了影响关节软骨再生的因素,然后提出了相应的治疗策略,最后指出了未来的研究方向。我们发现,调节机械敏感性离子通道的开放、调节HIF-1的表达、输送生长因子、清除衰老细胞可促进关节软骨再生微环境的形成。该研究为今后治疗 OA 提供了新思路,通过调节微环境促进关节软骨再生,从而达到治疗 OA 的目的。
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来源期刊
CiteScore
6.90
自引率
2.40%
发文量
423
审稿时长
15 weeks
期刊介绍: Journal of Immunology Research is a peer-reviewed, Open Access journal that provides a platform for scientists and clinicians working in different areas of immunology and therapy. The journal publishes research articles, review articles, as well as clinical studies related to classical immunology, molecular immunology, clinical immunology, cancer immunology, transplantation immunology, immune pathology, immunodeficiency, autoimmune diseases, immune disorders, and immunotherapy.
期刊最新文献
The Potential of Single-Chain Variable Fragment Antibody: Role in Future Therapeutic and Diagnostic Biologics. Taz/Tead1 Promotes Alternative Macrophage Activation and Kidney Fibrosis via Transcriptional Upregulation of Smad3. Promoting Articular Cartilage Regeneration through Microenvironmental Regulation. Exosome-Derived microRNA: Potential Target for Diagnosis and Treatment of Sepsis. Breastfeeding and Neonatal Age Influence Neutrophil-Driven Ontogeny of Blood Cell Populations in the First Week of Human Life.
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