Torres-Guzman Ricardo A, Avila Francisco R, Maita Karla C, Garcia John P, De Sario Gioacchino D, Borna Sahar, Eldaly Abdullah S, Quinones-Hinojosa Alfredo, Zubair Abba C, Ho Olivia A, Forte Antonio J
Division of Plastic Surgery, Mayo Clinic, 4500 San Pablo Rd., Jacksonville, FL 32224, USA.
Department of Neurosurgery, Mayo Clinic, Jacksonville, FL 32224, USA.
J Clin Med. 2023 Jun 15;12(12):4064. doi: 10.3390/jcm12124064.
The use of bone morphogenic protein and mesenchymal stem cells has shown promise in promoting bone regeneration in calvarial defects. However, a systematic review of the available literature is needed to evaluate the efficacy of this approach.
We comprehensively searched electronic databases using MeSH terms related to skull defects, bone marrow mesenchymal stem cells, and bone morphogenic proteins. Eligible studies included animal studies that used BMP therapy and mesenchymal stem cells to promote bone regeneration in calvarial defects. Reviews, conference articles, book chapters, and non-English language studies were excluded. Two independent investigators conducted the search and data extraction.
Twenty-three studies published between 2010 and 2022 met our inclusion criteria after a full-text review of the forty-five records found in the search. Eight of the 23 studies used mice as models, while 15 used rats. The most common mesenchymal stem cell was bone marrow-derived, followed by adipose-derived. BMP-2 was the most popular. Stem cells were embedded in Scaffold (13), Transduction (7), and Transfection (3), and they were delivered BMP to cells. Each treatment used 2 × 10-1 × 10 mesenchymal stem cells, averaging 2.26 × 10. Most BMP-transduced MSC studies used lentivirus.
This systematic review examined BMP and MSC synergy in biomaterial scaffolds or alone. BMP therapy and mesenchymal stem cells in calvarial defects, alone, or with a scaffold regenerated bone. This method treats skull defects in clinical trials. The best scaffold material, therapeutic dosage, administration method, and long-term side effects need further study.
骨形态发生蛋白和间充质干细胞在促进颅骨缺损的骨再生方面已显示出前景。然而,需要对现有文献进行系统综述以评估这种方法的疗效。
我们使用与颅骨缺损、骨髓间充质干细胞和骨形态发生蛋白相关的医学主题词全面搜索了电子数据库。符合条件的研究包括使用骨形态发生蛋白疗法和间充质干细胞促进颅骨缺损骨再生的动物研究。综述、会议文章、书籍章节和非英语语言研究被排除。两名独立研究人员进行了搜索和数据提取。
在对搜索中找到的45条记录进行全文审查后,2010年至2022年发表的23项研究符合我们的纳入标准。23项研究中有8项使用小鼠作为模型,15项使用大鼠。最常见的间充质干细胞是骨髓来源的,其次是脂肪来源的。骨形态发生蛋白-2最受欢迎。干细胞被嵌入支架(13项)、转导(7项)和转染(3项)中,并将骨形态发生蛋白递送至细胞。每种治疗使用2×10 - 1×10个间充质干细胞,平均为2.26×10个。大多数骨形态发生蛋白转导的间充质干细胞研究使用慢病毒。
本系统综述研究了骨形态发生蛋白和间充质干细胞在生物材料支架中或单独使用时的协同作用。骨形态发生蛋白疗法和间充质干细胞在颅骨缺损中单独或与支架一起可使骨再生。这种方法在临床试验中治疗颅骨缺损。最佳的支架材料、治疗剂量、给药方法和长期副作用需要进一步研究。