Hao Zichen, Li Jun, Li Bo, Alder Kareme D, Cahill Sean V, Munger Alana M, Lee Inkyu, Kwon Hyuk-Kwon, Back JungHo, Xu Shuogui, Kang Min-Jong, Lee Francis Y
Department of Orthopaedics and Rehabilitation, Yale University, School of Medicine, New Haven, CT, USA.
Department of Emergency and Trauma, Changhai Hospital, Navy Medical University, Shanghai, China.
J Bone Miner Res. 2021 Jan;36(1):186-198. doi: 10.1002/jbmr.4175. Epub 2020 Sep 24.
Smokers are at a higher risk of delayed union or nonunion after fracture repair. Few specific interventions are available for prevention because the molecular mechanisms that result in these negative sequelae are poorly understood. Murine models that mimic fracture healing in smokers are crucial in further understanding the local cellular and molecular alterations during fracture healing caused by smoking. We exposed three murine strains, C57BL/6J, 129X1/SvJ, and BALB/cJ, to cigarette smoke for 3 months before the induction of a midshaft transverse femoral osteotomy. We evaluated fracture healing 4 weeks after the osteotomy using radiography, micro-computed tomography (μCT), and biomechanical testing. Radiographic analysis demonstrated a significant decrease in the fracture healing capacity of smoking 129X1/SvJ mice. μCT results showed delayed remodeling of fracture calluses in all three strains after cigarette smoke exposure. Biomechanical testing indicated the most significant impairment in the functional properties of 129X1/SvJ in comparison with C57BL/6J and BALB/cJ mice after cigarette smoke exposure. Thus, the 129X1/SvJ strain is most suitable in simulating smoking-induced impaired fracture healing. Furthermore, in smoking 129X1/SvJ murine models, we investigated the molecular and cellular alterations in fracture healing caused by cigarette smoking using histology, flow cytometry, and multiplex cytokine/chemokine analysis. Histological analysis showed impaired chondrogenesis in cigarette smoking. In addition, the important reparative cell populations, including skeletal stem cells and their downstream progenitors, demonstrated decreased expansion after injury as a result of cigarette smoking. Moreover, significantly increased pro-inflammatory mediators and the recruitment of immune cells in fracture hematomas were demonstrated in smoking mice. Collectively, our findings demonstrate the significant cellular and molecular alterations during fracture healing impaired by smoking, including disrupted chondrogenesis, aberrant skeletal stem and progenitor cell activity, and a pronounced initial inflammatory response. © 2020 American Society for Bone and Mineral Research (ASBMR).
吸烟者在骨折修复后发生骨愈合延迟或骨不连的风险更高。由于导致这些不良后果的分子机制尚不清楚,因此几乎没有可用的特异性预防干预措施。模拟吸烟者骨折愈合的小鼠模型对于进一步了解吸烟引起的骨折愈合过程中的局部细胞和分子改变至关重要。我们在诱导股骨干中段横行截骨术前3个月,将C57BL/6J、129X1/SvJ和BALB/cJ这三种小鼠品系暴露于香烟烟雾中。我们在截骨术后4周,使用X线摄影、显微计算机断层扫描(μCT)和生物力学测试评估骨折愈合情况。X线摄影分析显示,吸烟的129X1/SvJ小鼠的骨折愈合能力显著下降。μCT结果显示,香烟烟雾暴露后,所有三个品系的骨折痂重塑均延迟。生物力学测试表明,与香烟烟雾暴露后的C57BL/6J和BALB/cJ小鼠相比,129X1/SvJ小鼠的功能特性受损最为显著。因此,129X1/SvJ品系最适合模拟吸烟引起的骨折愈合受损。此外,在吸烟的129X1/SvJ小鼠模型中,我们使用组织学、流式细胞术和多重细胞因子/趋化因子分析,研究了吸烟引起的骨折愈合过程中的分子和细胞改变。组织学分析显示吸烟会损害软骨形成。此外,重要的修复细胞群体,包括骨骼干细胞及其下游祖细胞,在损伤后因吸烟而显示出增殖减少。此外,吸烟小鼠骨折血肿中的促炎介质显著增加,免疫细胞募集也增加。总体而言,我们的研究结果表明,吸烟会导致骨折愈合过程中显著的细胞和分子改变,包括软骨形成中断、骨骼干细胞和祖细胞活动异常以及明显的初始炎症反应。©2020美国骨与矿物质研究学会(ASBMR)