间充质干细胞
Wnt信号通路
骨形态发生蛋白
骨形态发生蛋白2
细胞生物学
软骨发生
祖细胞
干细胞
脂肪生成
脱钙骨基质
再生(生物学)
骨愈合
化学
癌症研究
医学
生物
信号转导
解剖
体外
材料科学
生物化学
基因
放大器
数据库管理
光电子学
CMOS芯片
作者
Gaurav Aman Luther,Eric R. Wagner,Gaohui Zhu,Quan Kang,Qing Luo,Joseph D. Lamplot,Yang Bi,Xiaoji Luo,Jinyong Luo,Chad M. Teven,Qiong Shi,Stephanie H. Kim,Jian‐Li Gao,Enyi Huang,Ke Yang,Richard Rames,Xing Liu,Mi Li,Ning Hu,Hong Shu Liu
标识
DOI:10.2174/156652311795684777
摘要
Promoting osteogenic differentiation and efficacious bone regeneration have the potential to revolutionize the treatment of orthopaedic and musculoskeletal disorders. Mesenchymal Stem Cells (MSCs) are bone marrow progenitor cells that have the capacity to differentiate along osteogenic, chondrogenic, myogenic, and adipogenic lineages. Differentiation along these lineages is a tightly controlled process that is in part regulated by the Bone Morphogenetic Proteins (BMPs). BMPs 2 and 7 have been approved for clinical use because their osteoinductive properties act as an adjunctive treatment to surgeries where bone healing is compromised. BMP-9 is one of the least studied BMPs, and recent in vitro and in vivo studies have identified BMP-9 as a potent inducer of osteogenic differentiation in MSCs. BMP-9 exhibits significant molecular cross-talk with the Wnt/ β-catenin and other signaling pathways, and adenoviral expression of BMP-9 in MSCs increases the expression of osteogenic markers and induces trabecular bone and osteiod matrix formation. Furthermore, BMP-9 has been shown to act synergistically in bone formation with other signaling pathways, including Wnt/ β-catenin, IGF, and retinoid signaling pathways. These results suggest that BMP-9 should be explored as an effective bone regeneration agent, especially in combination with adjuvant therapies, for clinical applications such as large segmental bony defects, non-union fractures, and/or spinal fusions.
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