ten Dijke P
Department of Molecular and Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Curr Med Res Opin. 2006;22 Suppl 1:S7-11. doi: 10.1185/030079906X80576.
Bone morphogenetic proteins (BMPs) promote bone formation by stimulating the proliferation and differentiation of osteoblasts. It has been suggested that non-union of the bone, and delayed healing, may be the result of decreased levels of BMP activity. Activation of BMP receptors initiates phosphorylation of the downstream effector proteins, known as receptor-regulated Smads, leading to signal transduction. Receptor-regulated Smads form a hetero-oligomeric complex with a common mediator Smad, which translocates into the nucleus and regulates target gene transcription. The BMP signalling cascade is closely regulated, with the inhibitory Smads blocking the intracellular signal cascade. Extracellular antagonists, such as noggin, inhibit binding to BMP receptors. BMP-2 and BMP-7 have demonstrated clinical utility for bone regeneration, and are commercially available through the use of recombinant DNA technology.
骨形态发生蛋白(BMPs)通过刺激成骨细胞的增殖和分化来促进骨形成。有人提出,骨不连和愈合延迟可能是BMP活性水平降低的结果。BMP受体的激活引发下游效应蛋白(即受体调节型Smads)的磷酸化,从而导致信号转导。受体调节型Smads与一种共同的介质Smad形成异源寡聚体复合物,该复合物易位进入细胞核并调节靶基因转录。BMP信号级联受到密切调控,抑制性Smads会阻断细胞内信号级联。细胞外拮抗剂,如头蛋白,会抑制与BMP受体的结合。BMP-2和BMP-7已证明在骨再生方面具有临床应用价值,并且可通过重组DNA技术进行商业生产。