Yanagita Motoko
Kyoto University Graduate School of Medicine, Career-Path Promotion Unit for Young Life Scientists, Yoshida-konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Curr Opin Investig Drugs. 2010 Mar;11(3):315-22.
Bone morphogenetic proteins (BMPs) are phylogenetically conserved signaling molecules that belong to the TGFbeta superfamily and are involved in the morphogenesis, as well as the pathogenesis, of several disorders. The function of BMPs is regulated by BMP antagonists that bind directly to the proteins, thus inhibiting binding to the relevant receptors. Pharmacological doses of BMP-7 have been demonstrated to repair established renal injury and, thus, BMP antagonists modulating endogenous BMP-7 activities may be possible therapeutic targets for kidney disease. In this review, recent findings on the BMP antagonists that modify the function of BMP-7 in kidney disease are summarized, and possible implications for therapeutic strategies are discussed.
骨形态发生蛋白(BMPs)是在系统发育上保守的信号分子,属于转化生长因子β(TGFβ)超家族,参与多种疾病的形态发生以及发病机制。BMPs的功能由直接与这些蛋白结合的BMP拮抗剂调节,从而抑制与相关受体的结合。已证实药理剂量的BMP-7可修复已有的肾损伤,因此,调节内源性BMP-7活性的BMP拮抗剂可能是肾脏疾病的潜在治疗靶点。在本综述中,总结了关于在肾脏疾病中改变BMP-7功能的BMP拮抗剂的最新研究发现,并讨论了其对治疗策略的潜在影响。