Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Stem Cells Dev. 2021 May 1;30(9):473-484. doi: 10.1089/scd.2021.0011. Epub 2021 Apr 19.
Heterotopic ossification (HO) is a devastating condition in which ectopic bone forms inappropriately in soft tissues following traumatic injuries and orthopedic surgeries as a result of aberrant mesenchymal progenitor cell (MPC) differentiation. HO leads to chronic pain, decreased range of motion, and an overall decrease in quality of life. While several treatments have shown promise in animal models, all must be given during early stages of formation. Methods for early determination of whether and where endochondral ossification/soft tissue mineralization (HO anlagen) develop are lacking. At-risk patients are not identified sufficiently early in the process of MPC differentiation and soft tissue endochondral ossification for potential treatments to be effective. Hence, a critical need exists to develop technologies capable of detecting HO anlagen soon after trauma, when treatments are most effective. In this study, we investigate high frequency spectral ultrasound imaging (SUSI) as a noninvasive strategy to identify HO anlagen at early time points after injury. We show that by determining quantitative parameters based on tissue organization and structure, SUSI identifies HO anlagen as early as 1-week postinjury in a mouse model of burn/tenotomy and 3 days postinjury in a rat model of blast/amputation. We analyze single cell RNA sequencing profiles of the MPCs responsible for HO formation and show that the early tissue changes detected by SUSI match chondrogenic and osteogenic gene expression in this population. SUSI identifies sites of soft tissue endochondral ossification at early stages of HO formation so that effective intervention can be targeted when and where it is needed following trauma-induced injury. Furthermore, we characterize the chondrogenic to osteogenic transition that occurs in the MPCs during HO formation and correlate gene expression to SUSI detection of the HO anlagen.
异位骨化(HO)是一种破坏性疾病,在外伤和骨科手术后,由于间充质祖细胞(MPC)异常分化,异位骨在软组织中形成。HO 导致慢性疼痛、运动范围减小和整体生活质量下降。虽然几种治疗方法在动物模型中显示出前景,但都必须在形成的早期阶段进行。缺乏早期确定是否以及在何处形成软骨内骨化/软组织矿化(HO 前体)的方法。在 MPC 分化和软组织软骨内骨化的过程中,高危患者没有被足够早地识别出来,因此无法有效地进行潜在的治疗。因此,迫切需要开发能够在创伤后尽早检测到 HO 前体的技术,因为此时治疗效果最佳。在这项研究中,我们研究了高频光谱超声成像(SUSI)作为一种非侵入性策略,以在受伤后早期识别 HO 前体。我们表明,通过确定基于组织组织和结构的定量参数,SUSI 可以在烧伤/肌腱切开术的小鼠模型中在受伤后 1 周,在爆炸/截肢的大鼠模型中在受伤后 3 天识别出 HO 前体。我们分析了负责 HO 形成的 MPC 的单细胞 RNA 测序图谱,并表明 SUSI 检测到的早期组织变化与该群体中的软骨和成骨基因表达相匹配。SUSI 在 HO 形成的早期阶段识别软组织软骨内骨化的部位,以便在创伤后发生创伤时在需要的时间和地点对其进行有效干预。此外,我们描述了 HO 形成过程中 MPC 中发生的软骨向成骨的转变,并将基因表达与 SUSI 对 HO 前体的检测相关联。