Moreno-Miralles Isabel, Schisler Jonathan C, Patterson Cam
Carolina Cardiovascular Biology Center, USA.
Curr Opin Hematol. 2009 May;16(3):195-201. doi: 10.1097/MOH.0b013e32832a07d6.
The role of bone morphogenetic proteins (BMPs) in vasculogenesis is still not well understood, despite many recent developments in this area of research. In this review, we discuss the most recent studies that identify new critical mechanisms through which BMP signaling acts with a focus on angiogenesis.
New evidence brought to light over the last few years suggests that BMP-binding proteins, formerly thought of as antagonists, can also increase BMP activity under certain conditions. It has also recently been determined that components of the extracellular matrix are involved in the BMP signaling pathways that regulate angiogenesis. Through the BMP pathway, myosin-X and cyclooxygenase 2 serve as target genes that have been determined to play a role in blood vessel formation. BMPs also conduct Smad-independent signaling and crosstalk with other pathways. Finally, BMPs have been shown to play an antiangiogenic role in specific settings.
Better understanding of the BMP signaling pathway and its regulators can have potentially great effects on therapeutic strategies from cardiovascular disease to cancer.
尽管骨形态发生蛋白(BMPs)在血管生成方面的研究最近有许多进展,但人们对其在血管发生中的作用仍未完全了解。在本综述中,我们讨论了最新研究,这些研究确定了BMP信号传导发挥作用的新关键机制,重点是血管生成。
过去几年中发现的新证据表明,以前被认为是拮抗剂的BMP结合蛋白在某些条件下也可以增加BMP活性。最近还确定,细胞外基质的成分参与调节血管生成的BMP信号通路。通过BMP途径,肌球蛋白-X和环氧化酶2作为已确定在血管形成中起作用的靶基因。BMP还进行不依赖Smad的信号传导并与其他途径发生串扰。最后,已证明BMP在特定环境中发挥抗血管生成作用。
更好地了解BMP信号通路及其调节剂可能对从心血管疾病到癌症的治疗策略产生潜在的重大影响。