Elvas Filipe, Stroobants Sigrid, Wyffels Leonie
Molecular Imaging Center Antwerp, University of Antwerp, Universiteitsplein 1, Wilrijk, 2610, Belgium.
Department of Nuclear Medicine, Antwerp University Hospital, Wilrijkstraat 10, 2650, Edegem, Belgium.
Apoptosis. 2017 Aug;22(8):971-987. doi: 10.1007/s10495-017-1384-0.
Phosphatidylethanolamine (PE) is one of the most abundant phospholipids in mammalian plasma membranes. In healthy cells, PE resides predominantly in the inner leaflet of the cell membrane. In dead or dying cells on the other hand, PE is externalized to the outer leaflet of the plasma membrane. The exposure of PE on the cell surface has therefore become an attractive target for the molecular imaging of cell death using single-photon emission computed tomography (SPECT) and positron emission tomography (PET). This has motivated the development of PE-specific probes to measure cell death in vitro and non-invasively in vivo. In this review, we highlight the biological roles of PE on cell membranes, and PE exposure as a biomarker of cell death in disease processes, along with the use of PE-binding molecular probes to target PE for the characterization of cell death on a cellular and tissue level. We specifically emphasize the preclinical applications of radiolabeled duramycin for the non-invasive imaging of cell death in animal models of disease and in tumors after therapy. In addition, we discuss the clinical relevance, limitations and future perspectives of this imaging approach of cell death.
磷脂酰乙醇胺(PE)是哺乳动物质膜中含量最丰富的磷脂之一。在健康细胞中,PE主要存在于细胞膜的内小叶。另一方面,在死亡或濒死细胞中,PE会外化至质膜的外小叶。因此,细胞表面PE的暴露已成为使用单光子发射计算机断层扫描(SPECT)和正电子发射断层扫描(PET)对细胞死亡进行分子成像的一个有吸引力的靶点。这推动了用于体外测量细胞死亡和体内非侵入性测量细胞死亡的PE特异性探针的开发。在本综述中,我们强调了PE在细胞膜上的生物学作用,以及PE暴露作为疾病过程中细胞死亡生物标志物的作用,同时还介绍了使用PE结合分子探针靶向PE以在细胞和组织水平上表征细胞死亡的情况。我们特别强调了放射性标记短杆菌肽在疾病动物模型和治疗后肿瘤中细胞死亡非侵入性成像的临床前应用。此外,我们还讨论了这种细胞死亡成像方法的临床相关性、局限性和未来前景。