Naudot Marie, Davrou Julien, Djebara Az-Eddine, Barre Anaïs, Lavagen Nolwenn, Lardière Sandrine, Azdad Soufiane Zakaria, Zabijak Luciane, Lack Stéphane, Devauchelle Bernard, Marolleau Jean-Pierre, Le Ricousse Sophie
Research Unit 7516, CHIMERE, Jules Verne University of Picardie, Amiens, France.
Department of Maxillofacial Surgery, Pitié Salpêtrière Hospital, AP-HP, Paris, France.
Plast Reconstr Surg Glob Open. 2020 Apr 29;8(4):e2743. doi: 10.1097/GOX.0000000000002743. eCollection 2020 Apr.
One of the major difficulties in cleft palate repair is the requirement for several surgical procedures and autologous bone grafting to form a bony bridge across the cleft defect. Engineered tissue, composed of a biomaterial scaffold and multipotent stem cells, may be a useful alternative for minimizing the non-negligible risk of donor site morbidity. The present study was designed to confirm the healing and osteogenic properties of a novel alginate-based hydrogel in palate repair.
Matrix constructs, seeded with allogeneic bone marrow-derived mesenchymal stem cells (BM-MSCs) or not, were incorporated into a surgically created, critical-sized cleft palate defect in the rat. Control with no scaffold was also tested. Bone formation was assessed using microcomputed tomography at weeks 2, 4, 8, and 12 and a histologic analysis at week 12.
At 12 weeks, the proportion of bone filling associated with the use of hydrogel scaffold alone did not differ significantly from the values observed in the scaffold-free experiment (61.01% ± 5.288% versus 36.91% ± 5.132%; = 0.1620). The addition of BM-MSCs stimulated bone formation not only at the margin of the defect but also in the center of the implant.
In a relevant in vivo model of cleft palate in the rat, we confirmed the alginate-based hydrogel's biocompatibility and real advantages for tissue healing. Addition of BM-MSCs stimulated bone formation in the center of the implant, demonstrating the new biomaterial's potential for use as a bone substitute grafting material for cleft palate repair.
腭裂修复的主要困难之一是需要多次外科手术和自体骨移植来在腭裂缺损处形成骨桥。由生物材料支架和多能干细胞组成的工程组织可能是一种有用的替代方法,可将供体部位发病的不可忽视风险降至最低。本研究旨在证实一种新型藻酸盐基水凝胶在腭裂修复中的愈合和成骨特性。
将接种或未接种异体骨髓间充质干细胞(BM-MSCs)的基质构建体植入大鼠手术造成的临界尺寸腭裂缺损处。还测试了无支架对照。在第2、4、8和12周使用微型计算机断层扫描评估骨形成,并在第12周进行组织学分析。
在12周时,单独使用水凝胶支架的骨填充比例与无支架实验中观察到的值无显著差异(61.01%±5.288%对36.91%±5.132%;P = 0.1620)。添加BM-MSCs不仅刺激了缺损边缘的骨形成,还刺激了植入物中心的骨形成。
在大鼠腭裂的相关体内模型中,我们证实了藻酸盐基水凝胶的生物相容性及其在组织愈合方面的实际优势。添加BM-MSCs刺激了植入物中心的骨形成,证明了这种新型生物材料作为腭裂修复骨替代移植材料的潜在用途。