Shariati Kaavian, Bedar Meiwand, Huang Kelly X, Moghadam Shahrzad, Mirzaie Sarah, LaGuardia Jonnby S, Chen Wei, Kang Youngnam, Ren Xiaoyan, Lee Justine C
Division of Plastic & Reconstructive Surgery, University of California, Los Angeles David Geffen School of Medicine, Los Angeles, CA, 90095, USA.
Research Service, Greater Los Angeles VA Healthcare System, Los Angeles, CA, 91343, USA.
Adv Ther (Weinh). 2025 Jan;8(1). doi: 10.1002/adtp.202400296. Epub 2024 Nov 15.
Tissue regeneration involves dynamic dialogue between and among different cells and their surrounding matrices. Bone regeneration is specifically governed by reciprocity between osteoblasts and osteoclasts within the bone microenvironment. Osteoclast-directed resorption and osteoblast-directed formation of bone are essential to bone remodeling, and the crosstalk between these cells is vital to curating a sequence of events that culminate in the creation of bone tissue. Among bone biomaterial strategies, many have investigated the use of different material cues to direct the development and activity of osteoblasts. However, less attention has been given to exploring features that similarly target osteoclast formation and activity, with even fewer strategies demonstrating or integrating biomaterial-directed modulation of osteoblast-osteoclast coupling. This review aims to describe various biomaterial cues demonstrated to influence osteoclastogenesis and osteoclast function, emphasizing those that enhance a material construct's ability to achieve bone healing and regeneration. Additionally discussed are approaches that influence the communication between osteoclasts and osteoblasts, particularly in a manner that takes advantage of their coupling. Deepening our understanding of how biomaterial cues may dictate osteoclast differentiation, function, and influence on the microenvironment may enable the realization of bone-replacement interventions with enhanced integrative and regenerative capacities.
组织再生涉及不同细胞及其周围基质之间的动态对话。骨再生具体受骨微环境中成骨细胞和破骨细胞之间的相互作用调控。破骨细胞介导的骨吸收和成骨细胞介导的骨形成对骨重塑至关重要,这些细胞之间的相互作用对于策划一系列最终导致骨组织形成的事件至关重要。在骨生物材料策略中,许多研究都探讨了使用不同的材料线索来指导成骨细胞的发育和活性。然而,对于探索类似地靶向破骨细胞形成和活性的特征的关注较少,展示或整合生物材料介导的成骨细胞-破骨细胞偶联调节的策略甚至更少。本综述旨在描述已证明影响破骨细胞生成和破骨细胞功能的各种生物材料线索,重点强调那些增强材料构建体实现骨愈合和再生能力的线索。还讨论了影响破骨细胞和成骨细胞之间通讯的方法,特别是以利用它们偶联的方式。加深我们对生物材料线索如何决定破骨细胞分化、功能以及对微环境影响的理解,可能有助于实现具有增强整合和再生能力的骨替代干预措施。