Mater Research Institute-The University of Queensland, Translational Research Institute, Woolloongabba, Australia.
University of Versailles Saint Quentin en Yvelines, END:ICAP U1179 INSERM, UFR Simone Veil-Santé, Montigny le Bretonneux, France.
J Bone Miner Res. 2023 Nov;38(11):1700-1717. doi: 10.1002/jbmr.4905. Epub 2023 Sep 23.
Neurogenic heterotopic ossifications (NHO) are heterotopic bones that develop in periarticular muscles after severe central nervous system (CNS) injuries. Several retrospective studies have shown that NHO prevalence is higher in patients who suffer concomitant infections. However, it is unclear whether these infections directly contribute to NHO development or reflect the immunodepression observed in patients with CNS injury. Using our mouse model of NHO induced by spinal cord injury (SCI) between vertebrae T to T , we demonstrate that lipopolysaccharides (LPS) from gram-negative bacteria exacerbate NHO development in a toll-like receptor-4 (TLR4)-dependent manner, signaling through the TIR-domain-containing adapter-inducing interferon-β (TRIF/TICAM1) adaptor rather than the myeloid differentiation primary response-88 (MYD88) adaptor. We find that T to T SCI did not significantly alter intestinal integrity nor cause intestinal bacteria translocation or endotoxemia, suggesting that NHO development is not driven by endotoxins from the gut in this model of SCI-induced NHO. Relevant to the human pathology, LPS increased expression of osteoblast markers in cultures of human fibro-adipogenic progenitors isolated from muscles surrounding NHO biopsies. In a case-control retrospective study in patients with traumatic brain injuries, infections with gram-negative Pseudomonas species were significantly associated with NHO development. Together these data suggest a functional association between gram-negative bacterial infections and NHO development and highlights infection management as a key consideration to avoid NHO development in patients. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
神经源性异位骨化(NHO)是一种在严重中枢神经系统(CNS)损伤后的关节周围肌肉中形成的异位骨。几项回顾性研究表明,并发感染的患者 NHO 的患病率更高。然而,目前尚不清楚这些感染是否直接导致 NHO 的发展,还是反映了 CNS 损伤患者中观察到的免疫抑制。使用我们的 T 到 T 椎骨脊髓损伤(SCI)诱导的 NHO 小鼠模型,我们证明革兰氏阴性菌的脂多糖(LPS)通过 Toll 样受体 4(TLR4)依赖性方式加剧 NHO 的发展,通过 TIR 结构域包含衔接子诱导干扰素-β(TRIF/TICAM1)衔接子而不是髓样分化初级反应-88(MYD88)衔接子进行信号传递。我们发现 T 到 T SCI 并没有显著改变肠道完整性,也不会导致肠道细菌易位或内毒素血症,这表明在这种 SCI 诱导的 NHO 模型中,NHO 的发展不是由肠道内毒素驱动的。与人类病理学相关的是,LPS 增加了从围绕 NHO 活检的肌肉中分离出的人成纤维脂肪祖细胞培养物中骨细胞标志物的表达。在一项创伤性脑损伤患者的病例对照回顾性研究中,革兰氏阴性假单胞菌感染与 NHO 的发展显著相关。这些数据共同表明,革兰氏阴性细菌感染与 NHO 的发展之间存在功能关联,并强调感染管理是避免患者发生 NHO 发展的关键考虑因素。