Developmental BioEngineering Department, Faculty of Science and Technology and TechMed Centre, University of Twente, Enschede, The Netherlands.
Orthopaedic Biomechanics, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Tissue Eng Part A. 2022 Jun;28(11-12):478-499. doi: 10.1089/ten.TEA.2021.0226. Epub 2022 May 20.
Osteoarthritis (OA) and chronic low back pain due to degenerative (intervertebral) disc disease (DDD) are two of the major causes of disabilities worldwide, affecting hundreds of millions of people and leading to a high socioeconomic burden. Although OA occurs in synovial joints and DDD occurs in cartilaginous joints, the similarities are striking, with both joints showing commonalities in the nature of the tissues and in the degenerative processes during disease. Consequently, repair strategies for articular cartilage (AC) and nucleus pulposus (NP), the core of the intervertebral disc, in the context of OA and DDD share common aspects. One of such tissue engineering approaches is the use of injectable hydrogels for AC and NP repair. In this review, the state-of-the-art and recent developments in injectable hydrogels for repairing, restoring, and regenerating AC tissue suffering from OA and NP tissue in DDD are summarized focusing on cell-free approaches. The various biomaterial strategies exploited for repair of both tissues are compared, and the synergies that could be gained by translating experiences from one tissue to the other are identified. Impact statement Joints affected by osteoarthritis (OA) and degenerative (intervertebral) disc disease (DDD) share similarities in tissue composition and in the degenerative disease processes. This has led to the development of similar tissue engineering approaches to repair the articular cartilage (AC) and the nucleus pulposus (NP), in the context of OA and DDD, such as injectable hydrogels. In this review, recent developments in injectable hydrogels for repair of AC and NP tissues are summarized, biomaterial strategies are compared, and synergies are identified focusing on cell-free approaches. The summarized developments are expected to inspire more cross talk between both research fields.
骨关节炎 (OA) 和因退行性 (椎间) 盘疾病 (DDD) 引起的慢性下腰痛是全球两大主要致残原因,影响数亿人,并导致高社会经济负担。虽然 OA 发生在滑膜关节,DDD 发生在软骨关节,但两者之间存在惊人的相似之处,这两个关节在组织性质和疾病过程中的退行性变化方面具有共同点。因此,OA 和 DDD 背景下关节软骨 (AC) 和椎间盘核心部位的髓核 (NP) 的修复策略具有共同的方面。其中一种组织工程方法是使用可注射水凝胶修复 AC 和 NP。在本综述中,总结了用于修复 OA 中受损 AC 组织和 DDD 中 NP 组织的可注射水凝胶的最新进展,重点关注无细胞方法。比较了用于修复这两种组织的各种生物材料策略,并确定了通过将一种组织的经验转化到另一种组织中可以获得的协同作用。
关节受骨关节炎 (OA) 和退行性 (椎间) 盘疾病 (DDD) 的影响,其组织成分和退行性疾病过程具有相似性。这导致了在 OA 和 DDD 背景下,类似的组织工程方法的发展,如可注射水凝胶,用于修复关节软骨 (AC) 和髓核 (NP)。在本综述中,总结了用于修复 AC 和 NP 组织的可注射水凝胶的最新进展,比较了生物材料策略,并重点关注无细胞方法,确定了协同作用。预期总结的发展将激发这两个研究领域之间更多的交流。