Julius Wolff Institut, BIH at Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
BIH Center for Regenerative Therapies, BIH at Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Cells. 2023 Dec 24;13(1):40. doi: 10.3390/cells13010040.
The healing of a bone injury is a highly complex process involving a multitude of different tissue and cell types, including immune cells, which play a major role in the initiation and progression of bone regeneration.
We histologically analyzed the spatio-temporal occurrence of cells of the innate immune system (macrophages), the adaptive immune system (B and T lymphocytes), and bone cells (osteoblasts and osteoclasts) in the fracture area of a femoral osteotomy over the healing time. This study was performed in a bone osteotomy gap mouse model. We also investigated two key challenges of successful bone regeneration: hypoxia and revascularization.
Macrophages were present in and around the fracture gap throughout the entire healing period. The switch from initially pro-inflammatory M1 macrophages to the anti-inflammatory M2 phenotype coincided with the revascularization as well as the appearance of osteoblasts in the fracture area. This indicates that M2 macrophages are necessary for the restoration of vessels and that they also play an orchestrating role in osteoblastogenesis during bone healing. The presence of adaptive immune cells throughout the healing process emphasizes their essential role for regenerative processes that exceeds a mere pathogen defense. B and T cells co-localize consistently with bone cells throughout the healing process, consolidating their crucial role in guiding bone formation. These histological data provide, for the first time, comprehensive information about the complex interrelationships of the cellular network during the entire bone healing process in one standardized set up. With this, an overall picture of the spatio-temporal interplay of cellular key players in a bone healing scenario has been created.
A spatio-temporal distribution of immune cells, bone cells, and factors driving bone healing at time points that are decisive for this process-especially during the initial steps of inflammation and revascularization, as well as the soft and hard callus phases-has been visualized. The results show that the bone healing cascade does not consist of five distinct, consecutive phases but is a rather complex interrelated and continuous process of events, especially at the onset of healing.
骨损伤的愈合是一个高度复杂的过程,涉及多种不同的组织和细胞类型,包括免疫细胞,它们在骨再生的启动和进展中起主要作用。
我们在股骨截骨骨折区域的愈合时间内,通过组织学分析先天免疫系统(巨噬细胞)、适应性免疫系统(B 和 T 淋巴细胞)和骨细胞(成骨细胞和破骨细胞)在骨折区域的时空发生情况。本研究在骨截骨间隙小鼠模型中进行。我们还研究了成功骨再生的两个关键挑战:缺氧和再血管化。
巨噬细胞在整个愈合期内存在于骨折间隙及其周围。最初促炎 M1 巨噬细胞向抗炎 M2 表型的转变与再血管化以及成骨细胞在骨折区域的出现同时发生。这表明 M2 巨噬细胞对于血管的恢复是必要的,并且它们在骨愈合过程中成骨细胞的形成中也起着协调作用。适应性免疫细胞在整个愈合过程中的存在强调了它们在超出单纯病原体防御的再生过程中的重要作用。B 和 T 细胞在整个愈合过程中与骨细胞一致地共定位,巩固了它们在指导骨形成中的关键作用。这些组织学数据首次提供了关于在一个标准化设置中整个骨愈合过程中细胞网络复杂相互关系的全面信息。通过这种方式,创建了一个在骨愈合场景中细胞关键参与者时空相互作用的整体图景。
在对该过程具有决定性意义的时间点(尤其是在炎症和再血管化以及软、硬骨痂阶段的初始步骤),免疫细胞、骨细胞和驱动骨愈合的因素的时空分布已经可视化。结果表明,骨愈合级联反应不是由五个不同的、连续的阶段组成,而是一个复杂的相互关联和连续的过程,尤其是在愈合开始时。