Auriemma Renato, Sponchioni Mattia, Capasso Palmiero Umberto, Rossino Giacomo, Rossetti Arianna, Marsala Andrea, Collina Simona, Sacchetti Alessandro, Moscatelli Davide, Peviani Marco
Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via Mancinelli 7, 20131 Milano, Italy.
Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, 8093 Zürich, Switzerland.
Nanomaterials (Basel). 2021 Jun 28;11(7):1693. doi: 10.3390/nano11071693.
Reactive microgliosis is a pathological hallmark that accompanies neuronal demise in many neurodegenerative diseases, ranging from acute brain/spinal cord injuries to chronic diseases, such as amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD) and age-related dementia. One strategy to assess and monitor microgliosis is to use positron emission tomography (PET) by exploiting radioligands selective for the 18 kDa translocator protein (TSPO) which is highly upregulated in the brain in pathological conditions. Several TSPO ligands have been developed and validated, so far. Among these, PBR28 has been widely adopted for PET imaging at both preclinical and clinical levels, thanks to its high brain penetration and high selectivity. For this reason, PBR28 represents a good candidate for functionalization strategies, where this ligand could be exploited to drive selective targeting of TSPO-expressing cells. Since the PBR28 structure lacks functional moieties that could be exploited for derivatization, in this work we explored a synthetic pathway for the synthesis of a PBR28 derivative carrying an alkyne group (PBR-alkyne), enabling the fast conjugation of the ligand through azide-alkyne cycloaddition, also known as click-chemistry. As a proof of concept, we demonstrated in silico that the derivatized PBR28 ligand maintains the capability to fit into the TSPO binding pocked, and we successfully exploited PBR-alkyne to decorate zwitterionic biodegradable polymer nanoparticles (NPs) resulting in efficient internalization in cultured microglia-like cell lines.
反应性小胶质细胞增生是许多神经退行性疾病中伴随神经元死亡的病理标志,这些疾病范围从急性脑/脊髓损伤到慢性疾病,如肌萎缩侧索硬化症(ALS)、阿尔茨海默病(AD)和年龄相关性痴呆。评估和监测小胶质细胞增生的一种策略是利用正电子发射断层扫描(PET),通过利用对18 kDa转位蛋白(TSPO)具有选择性的放射性配体,该蛋白在病理条件下在大脑中高度上调。到目前为止,已经开发并验证了几种TSPO配体。其中,PBR28由于其高脑渗透性和高选择性,已在临床前和临床水平上广泛用于PET成像。因此,PBR28是功能化策略的良好候选者,在该策略中,该配体可用于驱动对表达TSPO的细胞进行选择性靶向。由于PBR28结构缺乏可用于衍生化的功能部分,在这项工作中,我们探索了一种合成途径,用于合成带有炔基的PBR28衍生物(PBR-炔烃),通过叠氮化物-炔烃环加成反应(也称为点击化学)实现配体的快速共轭。作为概念验证,我们在计算机模拟中证明,衍生化的PBR28配体保持了适合TSPO结合口袋的能力,并且我们成功地利用PBR-炔烃修饰两性离子可生物降解聚合物纳米颗粒(NPs),从而在培养的小胶质细胞样细胞系中实现有效内化。