Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Semin Nucl Med. 2017 Sep;47(5):553-575. doi: 10.1053/j.semnuclmed.2017.06.003. Epub 2017 Jul 13.
In this chapter, we provide a review of the challenges and advances in developing successful PET imaging agents for 3 major types of aggregated amyloid proteins: amyloid-beta (Aβ), tau, and alpha-synuclein (α-syn). These 3 amyloids are involved in the pathogenesis of a variety of neurodegenerative diseases, referred to as proteinopathies or proteopathies, that include Alzheimer disease, Lewy body dementias, multiple system atrophy, and frontotemporal dementias, among others. In the Introduction section, we briefly discuss the history of amyloid in neurodegenerative diseases and describe why progress in developing effective imaging agents has been hampered by the failure of crystallography to provide definitive ligand-protein interactions for rational radioligand design efforts. Instead, the field has relied on largely serendipitous, trial-and-error methods to achieve useful and specific PET amyloid imaging tracers for Aβ, tau, and α-syn deposits. Because many of the proteopathies involve more than 1 amyloid protein, it is important to develop selective PET tracers for the different amyloids to help assess the relative contribution of each to total amyloid burden. We use Pittsburgh compound B to illustrate some of the critical steps in developing a potent and selective Aβ PET imaging agent. Other selective Aβ and tau PET imaging compounds have followed similar pathways in their developmental processes. Success for selective α-syn PET imaging agents has not been realized yet, but work is ongoing in multiple laboratories throughout the world. In the tau sections, we provide background regarding 3-repeat (3R) and 4-repeat (4R) tau proteins and how they can affect the binding of tau radioligands in different tauopathies. We review the ongoing efforts to assess the properties of tau ligands, which are useful in 3R, 4R, or combined 3R-4R tauopathies. Finally, we describe in the α-syn sections recent attempts to develop selective tracers to image α-synucleinopathies.
在这一章中,我们将回顾开发成功的用于 3 种主要聚集态淀粉样蛋白的正电子发射断层扫描(PET)成像剂所面临的挑战和取得的进展,这 3 种淀粉样蛋白分别是β淀粉样蛋白(amyloid-beta,Aβ)、tau 蛋白和α-突触核蛋白(alpha-synuclein,α-syn)。这些淀粉样蛋白与多种神经退行性疾病的发病机制有关,这些疾病被称为蛋白病(proteinopathy)或蛋白相关疾病(proteopathy),包括阿尔茨海默病、路易体痴呆、多系统萎缩和额颞叶痴呆等。在引言部分,我们简要讨论了淀粉样蛋白在神经退行性疾病中的历史,并描述了为什么晶体学未能为合理配体-蛋白相互作用提供明确的信息,从而阻碍了开发有效成像剂的进展。相反,该领域主要依赖于偶然的、反复试验的方法,以实现用于 Aβ、tau 和 α-syn 沉积的有用且特异性的 PET 淀粉样蛋白成像示踪剂。由于许多蛋白病涉及不止一种淀粉样蛋白,因此开发针对不同淀粉样蛋白的选择性 PET 示踪剂来帮助评估每种淀粉样蛋白对总淀粉样蛋白负荷的相对贡献非常重要。我们使用匹兹堡化合物 B 来说明开发强效和选择性 Aβ PET 成像剂的一些关键步骤。其他选择性 Aβ 和 tau PET 成像化合物在其开发过程中也遵循了类似的途径。目前尚未成功开发出选择性的 α-syn PET 成像剂,但全世界多个实验室仍在进行相关工作。在 tau 部分,我们提供了关于 3 重复(3R)和 4 重复(4R)tau 蛋白的背景信息,以及它们如何影响不同 tau 病中 tau 配体的结合。我们回顾了评估 tau 配体特性的进展,这些特性对 3R、4R 或 3R-4R 混合 tau 病均有帮助。最后,我们在α-syn 部分描述了最近开发用于成像α-synucleinopathies 的选择性示踪剂的尝试。