Neutrophils are involved in early bone formation during midpalatal expansion

间质细胞 骨髓 细胞生物学 流式细胞术 血管生成 化学 男科 病理 医学 免疫学 生物 内科学
作者
Ting Jiang,Xin‐Yue Tang,Han Su,J Q Chen,Yu‐Qi Qin,Yu‐Chen Qin,Ningjuan Ouyang,Guo‐Hua Tang
出处
期刊:Oral Diseases [Wiley]
卷期号:30 (7): 4483-4494 被引量:7
标识
DOI:10.1111/odi.14849
摘要

Abstract Objective Midpalatal expansion (MPE) is routinely employed to treat transverse maxillary arch deficiency. Neutrophils are indispensable for recruiting bone marrow stromal cells (BMSCs) at the initial stage of bone regeneration. This study aimed to explore whether neutrophils participate in MPE and how they function during bone formation under mechanical stretching. Materials and Methods The presence and phenotype of neutrophils in the midpalatal suture during expansion were detected by flow cytometry and immunofluorescence staining. The possible mechanism of neutrophil recruitment and polarization was explored in vitro by exposing vascular endothelial cells (VECs) to cyclic tensile strain. Results The number of neutrophils in the distracted suture peaked on Day 3, and N2‐type neutrophils significantly increased on Day 5 after force application. The depletion of circulatory neutrophils reduced bone volume by 43.6% after 7‐day expansion. The stretched VECs recruited neutrophils via a CXCR2 mechanism in vitro, which then promoted BMSC osteogenic differentiation through the VEGFA/VEGFR2 axis. Consistently, these neutrophils showed higher expression of canonical N2 phenotype genes, including CD206 and Arg1. Conclusions These results suggested that neutrophils participated in early bone formation during MPE. Based on these findings, we propose that stretched VECs recruited and polarized neutrophils, which, in turn, induced BMSC osteogenic differentiation.
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