Kumari Neelam, Adhikari Anupriya, Bhagat Sunita, Mishra Anil K, Tiwari Anjani K
Division of Cyclotron and Radiopharmaceutical Sciences (DCRS), Institute of Nuclear Medicine and Allied Sciences (INMAS), Defence Research & Development Organization, Brig S K Mazumdar Road, Delhi, 110054, India.
Department of Chemistry, Sri Venkateswara College, University of Delhi, Delhi, India.
Mol Divers. 2025 Apr 21. doi: 10.1007/s11030-025-11192-9.
Translocator protein 18 kDa (TSPO) has been a salient target for probing and monitoring inflammation in the central nervous system (CNS) and peripheral systems. Leveraging our previously developed, TSPO specific, modified acetamidobenzoxazolone derivative, the present work describes the synthesis and development of an optical probe for lung inflammation imaging: 2-(3,6-dihydroxy-9H-xanthen-9-yl)-5-(3-(3-(2-(methyl(phenyl)amino)-2-oxoethyl)-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)thioureido)benzoic acid (FITC-MBP). The FITC-MBP is prepared through facile methodology by conjugating MBP to fluorophore dye FITC. Spectral properties remained equivalent to FITC dye with absorption and emission wavelength at 486 and 520 nm, respectively. Cellular uptake studies established overexpression of TSPO in lipopolysaccharide (LPS)-induced inflammation in H1299 lung cells. Reduced mean fluorescence intensity (MFI) during blocking experiments with PK11195 in flow cytometry suggests the specificity of the fluorescent probe towards TSPO. In-vivo optical imaging analysis on LPS-induced lung-inflamed balb/c mice revealed major sequestration of FITC-MBP in the lungs compared to control at 25 min post-injection that significantly decreased on pretreatment with PK11195 due to competitive binding to TSPO. On ground of these findings, we believe the novel fluorescent probe (FITC-MBP) might be utilized to visualize the overexpressed TSPO.
18 kDa转位蛋白(TSPO)一直是探测和监测中枢神经系统(CNS)及外周系统炎症的重要靶点。利用我们之前开发的TSPO特异性修饰乙酰氨基苯并恶唑酮衍生物,本研究描述了一种用于肺部炎症成像的光学探针的合成与开发:2-(3,6-二羟基-9H-呫吨-9-基)-5-(3-(3-(2-(甲基(苯基)氨基)-2-氧代乙基)-2-氧代-2,3-二氢苯并[d]恶唑-5-基)硫脲基)苯甲酸(FITC-MBP)。FITC-MBP通过将MBP与荧光染料FITC共轭的简便方法制备。光谱特性与FITC染料相当,吸收和发射波长分别为486和520 nm。细胞摄取研究证实了TSPO在脂多糖(LPS)诱导的H1299肺细胞炎症中过表达。流式细胞术中用PK11195进行阻断实验期间平均荧光强度(MFI)降低,表明荧光探针对TSPO具有特异性。对LPS诱导的肺部炎症的balb/c小鼠进行的体内光学成像分析显示,与对照组相比,注射后25分钟时FITC-MBP在肺部大量滞留,由于与TSPO的竞争性结合,在用PK11195预处理后显著降低。基于这些发现,我们认为新型荧光探针(FITC-MBP)可用于可视化过表达的TSPO。