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Bone morphogenetic proteins for articular cartilage regeneration

机译:用于关节软骨再生的骨形态发生蛋白

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摘要

Degeneration of articular cartilage (AC) tissue is the most common cause of osteoarthritis (OA) and rheumatoid arthritis. Bone morphogenetic proteins (BMPs) play important roles in bone and cartilage formation. This article reviews the experimental and clinical applications of BMPs in cartilage regeneration. Experimental evidence indicates that BMPs play an important role in protection against cartilage damage caused by inflammation or trauma, by binding to different receptor combinations and, consequently, activating different intracellular signaling pathways. Loss of function of BMP-related receptors contributes to the decreased intrinsic repair capacity of damaged cartilage and, thus, the multifunctional effects of BMPs make them attractive tools for the treatment of cartilage damage in patients with degenerative diseases. However, the development of BMP therapy as a treatment modality for cartilage regeneration has been hampered by certain factors, such as the eligibility of participants in clinical trials, financial support, drug delivery carrier safety, availabilities of effective scaffolds, appropriate selection of optimal dose and timing of administration, and side effects. Further research is needed to overcome these issues for future routine clinical applications. Research and development leading to the successful application of BMPs can initiate a new era in the treatment of cartilage degenerative diseases like OA.
机译:关节软骨(AC)组织的退化是骨关节炎(OA)和类风湿性关节炎的最常见原因。骨形态发生蛋白(BMPS)在骨和软骨形成中起重要作用。本文综述了BMP在软骨再生中的实验和临床应用。实验证据表明,BMPS通过与不同的受体组合结合,并因此激活不同的细胞内信号传导途径来保护炎症或创伤引起的软骨损伤的重要作用。与BMP相关的受体功能的丧失有助于降低受损软骨的内在修复能力,因此,BMP的多功能效应使其成为治疗退行性疾病患者软骨损伤的有吸引力的工具。 However, the development of BMP therapy as a treatment modality for cartilage regeneration has been hampered by certain factors, such as the eligibility of participants in clinical trials, financial support, drug delivery carrier safety, availabilities of effective scaffolds, appropriate selection of optimal dose and管理时间和副作用。需要进一步研究以克服未来常规临床应用的这些问题。导致BMPS成功应用的研究和开发可以在oa等软骨退行性疾病治疗中启动新时代。

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