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BMP-9 诱导间充质干细胞成骨分化:分子机制与治疗潜力。

BMP-9 induced osteogenic differentiation of mesenchymal stem cells: molecular mechanism and therapeutic potential.

机构信息

Molecular Oncology Laboratory, Department of Surgery, The University of Chicago Medical Center, IL 60637, USA.

出版信息

Curr Gene Ther. 2011 Jun;11(3):229-40. doi: 10.2174/156652311795684777.

DOI:10.2174/156652311795684777
PMID:21453282
Abstract

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.

摘要

促进成骨分化和有效的骨再生有可能彻底改变骨科和肌肉骨骼疾病的治疗方法。间充质干细胞(MSCs)是骨髓祖细胞,具有沿着成骨、软骨、肌和脂肪谱系分化的能力。沿着这些谱系的分化是一个严格控制的过程,部分受骨形态发生蛋白(BMPs)的调节。BMP-2 和 BMP-7 已被批准用于临床,因为它们的成骨诱导特性可作为手术的辅助治疗,这些手术中骨愈合受到损害。BMP-9 是研究最少的 BMP 之一,最近的体外和体内研究表明 BMP-9 是 MSCs 成骨分化的有效诱导剂。BMP-9 与 Wnt/β-catenin 和其他信号通路表现出显著的分子交叉对话,并且在 MSCs 中腺病毒表达 BMP-9 会增加成骨标志物的表达并诱导小梁骨和骨样基质的形成。此外,BMP-9 已被证明与其他信号通路(包括 Wnt/β-catenin、IGF 和视黄醇信号通路)在骨形成中具有协同作用。这些结果表明,BMP-9 应该作为一种有效的骨再生剂进行探索,特别是与辅助疗法结合使用,用于临床应用,例如大段骨缺损、骨不连骨折和/或脊柱融合。

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