Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Spine Institute, Shanghai Academy of Traditional Chinese Medicine, Shanghai, 200032, China.
BMC Musculoskelet Disord. 2021 May 28;22(1):494. doi: 10.1186/s12891-021-04360-z.
Macrophages and inflammatory cytokines play important roles in bone fracture healing. However, the expression patterns of macrophages and inflammatory cytokines during fracture healing under the condition of postmenopausal osteoporosis have not been fully revealed.
Tibia transverse fracture was established 12 weeks after ovariectomy or sham operation in 16-week old female mice. Tibias were harvested before fracture or 1, 3, 5, 7, 14, 21, 28 days after fracture for radiological and histological examinations. M1/M2 inflammatory macrophages, osteal macrophages and gene expressions of tumor necrosis factor-α, interleukin-6, interleukin-1β and macrophage conversion related molecules in the fracture haematoma or callus were also detected.
The processes of fracture healing, especially the phases of endochondral ossification and callus remodeling, were delayed in ovariectomized mice. The expressions of tumor necrosis factor-α and interleukin-6, but not interleukin-1β, in the fracture haematoma or callus were disturbed. Expressions of tumor necrosis factor-α were decreased at 1, 14 and 21 days post-fracture (DPF), and were increased at 3, 5 and 7 DPF. Interleukin-6 expressions at 1, 3 and 21 DPF were significantly increased. We found the decreases in M1 and M2 macrophages at 1 DPF of the initial inflammatory stage. M2 macrophages at 14 DPF of the middle stage and osteal macrophages at 14, 21 and 28 DPF of the middle and late stages of fracture healing were also reduced in ovariectomized mice.
The expressions of macrophages and inflammatory cytokines were impaired in ovariectomized mice, which might contribute partially to poor fracture healing.
巨噬细胞和炎症细胞因子在骨折愈合中发挥重要作用。然而,在绝经后骨质疏松症的情况下,骨折愈合过程中巨噬细胞和炎症细胞因子的表达模式尚未完全揭示。
在 16 周龄雌性小鼠中,在卵巢切除或假手术后 12 周建立胫骨横断骨折。在骨折前或骨折后 1、3、5、7、14、21、28 天采集胫骨进行影像学和组织学检查。还检测了血肿或骨痂中的 M1/M2 炎性巨噬细胞、成骨巨噬细胞以及肿瘤坏死因子-α、白细胞介素-6、白细胞介素-1β和巨噬细胞转化相关分子的基因表达。
骨折愈合过程,特别是软骨内骨化和骨痂重塑阶段,在去卵巢小鼠中延迟。血肿或骨痂中肿瘤坏死因子-α和白细胞介素-6(而非白细胞介素-1β)的表达受到干扰。骨折后 1、14 和 21 天(DPF)肿瘤坏死因子-α的表达降低,而在 3、5 和 7 DPF 时增加。白细胞介素-6 在 1、3 和 21 DPF 的表达显著增加。我们发现初始炎症阶段的 1 DPF 时 M1 和 M2 巨噬细胞减少。中间阶段的 14 DPF 时 M2 巨噬细胞和中间及晚期的 14、21 和 28 DPF 时成骨巨噬细胞在去卵巢小鼠中也减少。
巨噬细胞和炎症细胞因子的表达在去卵巢小鼠中受损,这可能部分导致骨折愈合不良。