干细胞分化和成骨过程中的 BMP9 信号传导

IF 1.5 Q4 CELL BIOLOGY American journal of stem cells Pub Date : 2013-03-08 Print Date: 2013-01-01
Joseph D Lamplot, Jiaqiang Qin, Guoxin Nan, Jinhua Wang, Xing Liu, Liangjun Yin, Justin Tomal, Ruidong Li, Wei Shui, Hongyu Zhang, Stephanie H Kim, Wenwen Zhang, Jiye Zhang, Yuhan Kong, Sahitya Denduluri, Mary Rose Rogers, Abdullah Pratt, Rex C Haydon, Hue H Luu, Jovito Angeles, Lewis L Shi, Tong-Chuan He
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引用次数: 0

摘要

骨形态发生蛋白(BMPs)是 TGF-β 超家族的成员,在骨骼发育、骨形成和干细胞分化中发挥着关键作用。BMP 信号传导中断会导致各种骨骼和骨骼外异常。BMP9是BMP家族中一个特征不明显的成员,也是成骨性最强的BMP之一,在体外和体内都能促进间充质干细胞(MSCs)的成骨分化。各种体内和分子研究的最新发现强烈表明,BMP9 介导的骨诱导机制与其他成骨 BMP 不同。已发现许多具有不同功能的信号通路在 BMP9 介导的成骨过程中发挥作用。其中一些途径在其他细胞系(包括脂肪细胞和软骨细胞)的分化过程中也至关重要。众所周知,BMP9 是一种强效的成骨因子,但它也影响其他几种途径,包括癌症发展、血管生成和肌肉生成。虽然 BMP9 已被证明是最具成骨作用的 BMP 之一,但人们对其产生这些作用的具体机制却知之甚少。在动物模型中,BMP9 在促进脊柱融合和骨性不愈合修复方面具有疗效,显示出巨大的转化前景。本综述旨在总结我们目前对 BMP9 介导的成骨作用的认识,介绍最近完成的工作,这些工作可能有助于我们进一步阐明这些途径。
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BMP9 signaling in stem cell differentiation and osteogenesis.

Bone morphogenetic proteins (BMPs) are members of the TGF-β superfamily and play a critical role in skeletal development, bone formation and stem cell differentiation. Disruptions in BMP signaling result in a variety of skeletal and extraskeletal anomalies. BMP9 is a poorly characterized member of the BMP family and is among the most osteogenic BMPs, promoting osteoblastic differentiation of mesenchymal stem cells (MSCs) both in vitro and in vivo. Recent findings from various in vivo and molecular studies strongly suggest that the mechanisms governing BMP9-mediated osteoinduction differ from other osteogenic BMPs. Many signaling pathways with diverse functions have been found to play a role in BMP9-mediated osteogenesis. Several of these pathways are also critical in the differentiation of other cell lineages, including adipocytes and chondrocytes. While BMP9 is known to be a potent osteogenic factor, it also influences several other pathways including cancer development, angiogenesis and myogenesis. Although BMP9 has been demonstrated as one of the most osteogenic BMPs, relatively little is known about the specific mechanisms responsible for these effects. BMP9 has demonstrated efficacy in promoting spinal fusion and bony non-union repair in animal models, demonstrating great translational promise. This review aims to summarize our current knowledge of BMP9-mediated osteogenesis by presenting recently completed work which may help us to further elucidate these pathways.

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