Application of a BMP2-binding heparan sulphate to promote periodontal regeneration.

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING
B Q Le, J H Too, T C Tan, R Aa Smith, V Nurcombe, S M Cool, N Yu
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引用次数: 3

Abstract

Periodontitis is the most common inflammatory disease that leads to periodontal defects and tooth loss. Regeneration of alveolar bone and soft tissue in periodontal defects is highly desirable but remains challenging. A heparan sulphate variant (HS3) with enhanced affinity for bone morphogenetic protein-2 (BMP2) that, when combined with collagen or ceramic biomaterials, enhances bone tissue regeneration in the axial and cranial skeleton in several animal models was reported previously. In the current study, establishing the efficacy of a collagen/HS3 device for the regeneration of alveolar bone and the adjacent periodontal apparatus and related structures was sought. Collagen sponges loaded with phosphate-buffered saline, HS3, BMP2, or HS3 + BMP2 were implanted into surgically-created intra-bony periodontal defects in rat maxillae. At the 6 week end- point the maxillae were decalcified, and the extent of tissue regeneration determined by histomorphometrical analysis. The combination of collagen/HS3, collagen/BMP2 or collagen/HS3 + BMP2 resulted in a three to four-fold increase in bone regeneration and up to a 1.5 × improvement in functional ligament restoration compared to collagen alone. Moreover, the combination of collagen/HS3 + BMP2 improved the alveolar bone height and reduced the amount of epithelial growth in the apical direction. The implantation of a collagen/ HS3 combination device enhanced the regeneration of alveolar bone and associated periodontal tissues at amounts comparable to collagen in combination with the osteogenic factor BMP2. This study highlights the efficacy of a collagen/HS3 combination device for periodontal regeneration that warrants further development as a point-of-care treatment for periodontitis-related bone and soft tissue loss.

结合bmp2的硫酸肝素促进牙周再生的应用。
牙周炎是最常见的炎症性疾病,可导致牙周缺损和牙齿脱落。牙周缺损的牙槽骨和软组织的再生是非常理想的,但仍然具有挑战性。硫酸肝素变体(HS3)与骨形态发生蛋白-2 (BMP2)的亲和力增强,当与胶原或陶瓷生物材料结合时,在几种动物模型中增强轴骨和颅骨骨骼的骨组织再生。在本研究中,我们试图建立胶原/HS3装置对牙槽骨和邻近牙周组织及相关结构的再生效果。将载有磷酸盐缓冲盐水、HS3、BMP2或HS3 + BMP2的胶原海绵植入手术造成的大鼠上颌骨内牙周缺损。6周结束时,上颌骨脱钙,组织形态计量学分析组织再生程度。与单独使用胶原蛋白相比,胶原蛋白/HS3、胶原蛋白/BMP2或胶原蛋白/HS3 + BMP2的组合可使骨再生增加3 - 4倍,功能韧带恢复提高1.5倍。胶原/HS3 + BMP2联合使用可提高牙槽骨高度,减少牙槽骨尖方向上皮细胞的生长。胶原/ HS3组合装置的植入促进了牙槽骨和相关牙周组织的再生,其量与胶原与成骨因子BMP2的组合相当。这项研究强调了胶原/HS3组合装置对牙周再生的功效,值得进一步开发,作为牙周炎相关骨和软组织损失的即时治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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