Neutrophils contribute to fracture healing by synthesizing fibronectin+ extracellular matrix rapidly after injury

被引:80
作者
Bastian, Okan W. [1 ]
Koenderman, Leo [2 ]
Alblas, Jacqueline [3 ]
Leenen, Luke P. H. [1 ]
Blokhuis, Taco J. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Traumatol, Heidelberglaan 100,HP G04-228, NL-3508 GA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Pulm Dis, Heidelberglaan 100,HP G04-228, NL-3508 GA Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Orthoped, Heidelberglaan 100,HP G04-228, NL-3508 GA Utrecht, Netherlands
关键词
Osteoimmunology; Bone; Regeneration; Repair; Inflammation; Leukocytes; POLYMORPHONUCLEAR NEUTROPHILS; INFLAMMATORY RESPONSE; RATS; FIBROBLASTS; HEMATOMA; CELLS;
D O I
10.1016/j.clim.2016.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The role of inflammatory cells in bone regeneration remains unclear. We hypothesize that leukocytes contribute to fracture healing by rapidly synthesizing an "emergency extracellular matrix (ECM)" before stromal cells infiltrate the fracture hematoma (FH) and synthesize the eventual collagenous bone tissue. 53 human FHs were isolated at different time points after injury, ranging from day 0 until day 23 after trauma and stained using (immuno)histochemistry. FHs isolated within 48 h after injury contained fibronectin(+) ECM, which increased over time. Neutrophils within the early FHs stained positive for cellular fibronectin and neutrophil derived particles were visible within the fibronectin(+) ECM. Stromal cells appeared at day 5 after injury or later and collagen type I birefringent fibrils could be identified during the second week after injury. Our study suggests that neutrophils contribute to bone regeneration by synthesizing an "emergency ECM" before stromal cells infiltrate the FH and synthesize the eventual bone tissue. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
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