Choi Hyuck, Jeong Byung-Chul, Hur Sung-Woong, Kim Jung-Woo, Lee Keun-Bae, Koh Jeong-Tae
Department of Pharmacology and Dental Therapeutics, Research Center for Biomineralization Disorders, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.
Department of Orthopedic Surgery, Chonnam National University Medical School and Hospital, Gwangju, Republic of Korea.
PLoS One. 2015 Oct 14;10(10):e0140502. doi: 10.1371/journal.pone.0140502. eCollection 2015.
Craniofacial bone defects are observed in a variety of clinical situations, and their reconstructions require coordinated coupling between angiogenesis and osteogenesis. In this study, we explored the effects of cartilage oligomeric matrix protein-angiopoietin 1 (COMP-Ang1), a synthetic and soluble variant of angiopoietin 1, on bone morphogenetic protein 2 (BMP2)-induced cranial bone regeneration, and recruitment and osteogenic differentiation of perivascular pericytes. A critical-size calvarial defect was created in the C57BL/6 mouse and COMP-Ang1 and/or BMP2 proteins were delivered into the defects with absorbable collagen sponges. After 3 weeks, bone regeneration was evaluated using micro-computed tomography and histologic examination. Pericyte recruitment into the defects was examined using immunofluorescence staining with anti-NG2 and anti-CD31 antibodies. In vitro recruitment and osteoblastic differentiation of pericyte cells were assessed with Boyden chamber assay, staining of calcified nodules, RT-PCR and Western blot analyses. Combined administration of COMP-Ang1 and BMP2 synergistically enhanced bone repair along with the increased population of CD31 (an endothelial cell marker) and NG2 (a specific marker of pericyte) positive cells. In vitro cultures of pericytes consistently showed that pericyte infiltration into the membrane pore of Boyden chamber was more enhanced by the combination treatment. In addition, the combination further increased the osteoblast-specific gene expression, including bone sialoprotein (BSP), osteocalcin (OCN) and osterix (OSX), phosphorylation of Smad/1/5/8, and mineralized nodule formation. COMP-Ang1 can enhance BMP2-induced cranial bone regeneration with increased pericyte recruitment. Combined delivery of the proteins might be a therapeutic strategy to repair cranial bone damage.
颅面骨缺损在多种临床情况下均可观察到,其修复需要血管生成与骨生成之间的协同偶联。在本研究中,我们探讨了血管生成素1的合成可溶性变体软骨寡聚基质蛋白 - 血管生成素1(COMP - Ang1)对骨形态发生蛋白2(BMP2)诱导的颅骨再生以及血管周围周细胞的募集和成骨分化的影响。在C57BL / 6小鼠中制造临界大小的颅骨缺损,并用可吸收胶原海绵将COMP - Ang1和/或BMP2蛋白递送至缺损处。3周后,使用微型计算机断层扫描和组织学检查评估骨再生情况。使用抗NG2和抗CD31抗体的免疫荧光染色检查周细胞向缺损处的募集情况。通过Boyden小室试验、钙化结节染色、RT - PCR和蛋白质印迹分析评估周细胞在体外的募集和成骨细胞分化情况。COMP - Ang1和BMP2联合给药协同增强了骨修复,同时CD31(内皮细胞标志物)和NG2(周细胞特异性标志物)阳性细胞数量增加。周细胞的体外培养始终表明,联合治疗更能增强周细胞向Boyden小室膜孔的浸润。此外,联合治疗进一步增加了成骨细胞特异性基因的表达,包括骨唾液酸蛋白(BSP)、骨钙素(OCN)和osterix(OSX),Smad/1/5/8的磷酸化以及矿化结节的形成。COMP - Ang1可通过增加周细胞募集来增强BMP2诱导的颅骨再生。联合递送这些蛋白质可能是修复颅骨损伤的一种治疗策略。