Osteogenic Small Molecule FK506 for Enhanced Bone Formation in a Rabbit Ankle Fusion Model.

IF 2.1 3区 医学 Q2 ORTHOPEDICS
Nicholas Huffman, Amogh Magesh, Hanna Solomon, Caroline Dingler, Sreedhara Sangadala, Jay M Patel, Jason T Bariteau
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Abstract

Non-union remains a significant complication following ankle fusion procedures, underscoring the need for effective osteogenic adjuvants to improve boney healing and fusion outcomes. This study investigates the osteogenic potential of FK506 (Tacrolimus), both in vitro and in vivo, for enhanced ankle fusion. Known orthobiologics in the market, such as recombinant human platelet-derived growth factor-BB (rhPDGF-BB), have been utilized to promote bone healing and were included in this study to assess their comparative and combinatory effects with FK506. Bovine marrow-derived cells (MDCs) were cultured in 2D and 3D environments to assess temporal markers of osteogenesis: RUNX2 nuclear localization (early), Alizarin Red S staining (intermediate), and mineral deposition with micro-computed tomography (late). A rabbit ankle fusion model (t = 4 weeks) was utilized to evaluate FK506's early in vivo efficacy. In 2D cultures, FK506 resulted in an increase, but rhPDGF-BB and the combination of rhPDGF-BB and FK506 yielded the highest mineral deposition. However, in 3D fibrin gel cultures, FK506 alone demonstrated the greatest bone volume and tissue mineralization. In vivo rabbit ankle studies revealed that while ankle joint fusion was not achieved, FK506-treated animals consistently showed substantial bone formation anterior to the joint, indicating its potential for localized osteogenesis in the ankle environment. This study demonstrates FK506's osteogenic potential as a standalone or combinatorial therapy. These findings highlight the need for further optimization of FK506 delivery methods and fixation strategies to maximize its clinical utility in ankle fusion procedures. Statement of Clinical Significance: The investigation of FK506 represents a potential pharmacological strategy for enhancing fusion healing and improving patient outcomes.

成骨小分子FK506在兔踝关节融合模型中促进骨形成。
骨不连仍然是踝关节融合术后的一个重要并发症,因此需要有效的成骨佐剂来改善骨愈合和融合术的结果。本研究探讨了FK506(他克莫司)在体外和体内增强踝关节融合的成骨潜能。市场上已知的骨科药物,如重组人血小板衍生生长因子- bb (rhPDGF-BB),已被用于促进骨愈合,并被纳入本研究,以评估它们与FK506的比较和联合作用。牛骨髓源性细胞(MDCs)在二维和三维环境中培养,以评估成骨的时间标记:RUNX2核定位(早期),茜素红S染色(中期),显微计算机断层扫描(晚期)的矿物沉积。采用兔踝关节融合模型(t = 4周)评价FK506的早期体内疗效。在2D培养中,FK506导致了矿物质沉积的增加,但rhPDGF-BB以及rhPDGF-BB和FK506的组合产生了最高的矿物质沉积。然而,在三维纤维蛋白凝胶培养中,FK506单独表现出最大的骨体积和组织矿化。兔踝关节体内研究显示,虽然踝关节未实现融合,但fk506治疗的动物在关节前一致显示出大量的骨形成,表明其在踝关节环境中具有局部成骨的潜力。这项研究证明了FK506作为单独或联合治疗的成骨潜力。这些发现强调需要进一步优化FK506的运送方法和固定策略,以最大化其在踝关节融合手术中的临床应用。临床意义声明:FK506的研究代表了一种潜在的增强融合愈合和改善患者预后的药理学策略。
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
Journal of Orthopaedic Research®
Journal of Orthopaedic Research® 医学-整形外科
CiteScore
6.10
自引率
3.60%
发文量
261
审稿时长
3-6 weeks
期刊介绍: The Journal of Orthopaedic Research is the forum for the rapid publication of high quality reports of new information on the full spectrum of orthopaedic research, including life sciences, engineering, translational, and clinical studies.
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