Carlson William D, Keck Peter C, Bosukonda Dattatreyamurty, Carlson Frederic Roy
Division of Cardiology, Mass General Hospital/Harvard, Boston, MA, United States.
Harvard Medical School, Boston, MA, United States.
Front Pharmacol. 2022 Jul 8;13:864509. doi: 10.3389/fphar.2022.864509. eCollection 2022.
Growth Factors have been evaluated as therapeutic targets for the treatment of a broad spectrum of diseases. Because they are proteins with pleiotropic effects, the quest to harness their beneficial effects has presented challenges. Most Growth Factors operate at the extracellular-receptor level and have natural feedback mechanisms that modulate their effects. As proteins, they are difficult and expensive to manufacture. Frequently proteins must be administered parenterally, may invoke an immune response, and may be neutralized by naturally occurring inhibitors. To circumvent these limitations, we have undertaken an effort to develop mimetics for the Bone Morphogenetic Protein (BMP) signaling pathway effects that incorporate the beneficial effects, eliminate the deleterious effects, and thereby create effective drug-like compounds.To this end, we have designed and tested a family of small peptide BMP mimetics. The design used the three-dimensional structure of BMP-7 to identify likely active surface regions. Lead sequences were then optimized based on assays that examine the selective binding to BMP receptors, demonstrate the phosphorylation of Smad-1,5,8, detect anti-apoptosis and anti-inflammation, and block the epithelial to mesenchymal transition (EMT) in renal tubular epithelial cells. These sequences were further optimized using assays of the attenuation of acute kidney injury in a rat-model of unilateral clamp ischemic reperfusion. This process uses a Structure Variance Analysis algorithm (SVA) to identify structure/activity relationships. One member of this family, THR-184, is an agonist of BMP signaling and a potent antagonist of TGFβ signaling. This small peptide mimetic inhibits inflammation, apoptosis, fibrosis and reverses epithelial to mesenchymal transition (EMT) by regulating multiple signaling pathways involved in the cellular injury of multiple organs. Its effects have been shown to control Acute Kidney Injury (AKI). THR-184 has progressed through phase I and II clinical trials for the prevention of Cardio-Vascular Surgery (CVS) associated AKI. This work provides a roadmap for the development of other growth factor mimetics and demonstrates how we might harness their therapeutic potential.
生长因子已被评估为治疗多种疾病的治疗靶点。由于它们是具有多效性的蛋白质,利用其有益作用的探索面临诸多挑战。大多数生长因子在细胞外受体水平发挥作用,并具有调节其作用的天然反馈机制。作为蛋白质,它们的生产困难且成本高昂。蛋白质通常必须通过肠胃外给药,可能引发免疫反应,并且可能被天然存在的抑制剂中和。为了克服这些限制,我们致力于开发模拟骨形态发生蛋白(BMP)信号通路效应的模拟物,这些模拟物兼具有益作用、消除有害作用,从而创造出有效的类药物化合物。为此,我们设计并测试了一系列小肽BMP模拟物。该设计利用BMP-7的三维结构来确定可能的活性表面区域。然后基于检测与BMP受体的选择性结合、证明Smad-1、5、8的磷酸化、检测抗凋亡和抗炎作用以及阻断肾小管上皮细胞中的上皮-间质转化(EMT)的试验对先导序列进行优化。使用单侧夹闭缺血再灌注大鼠模型中急性肾损伤的减轻试验进一步优化这些序列。这个过程使用结构方差分析算法(SVA)来确定结构/活性关系。该家族的一个成员THR-184是BMP信号的激动剂和TGFβ信号的强效拮抗剂。这种小肽模拟物通过调节参与多个器官细胞损伤的多种信号通路来抑制炎症、凋亡、纤维化并逆转上皮-间质转化(EMT)。其作用已被证明可控制急性肾损伤(AKI)。THR-184已完成预防心血管手术(CVS)相关AKI的I期和II期临床试验。这项工作为其他生长因子模拟物的开发提供了路线图,并展示了我们如何利用它们的治疗潜力。