Division of Pharmacology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Amsterdam University Medical Centers, University of Amsterdam, Amsterdam Neuroscience, Department of (Neuro)Pathology, Amsterdam, the Netherlands; Stichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands.
Cell Rep Med. 2024 Jun 18;5(6):101609. doi: 10.1016/j.xcrm.2024.101609.
ATP-binding cassette (ABC) transporters facilitate the movement of diverse molecules across cellular membranes, including those within the CNS. While most extensively studied in microvascular endothelial cells forming the blood-brain barrier (BBB), other CNS cell types also express these transporters. Importantly, disruptions in the CNS microenvironment during disease can alter transporter expression and function. Through this comprehensive review, we explore the modulation of ABC transporters in various brain pathologies and the context-dependent consequences of these changes. For instance, downregulation of ABCB1 may exacerbate amyloid beta plaque deposition in Alzheimer's disease and facilitate neurotoxic compound entry in Parkinson's disease. Upregulation may worsen neuroinflammation by aiding chemokine-mediated CD8 T cell influx into multiple sclerosis lesions. Overall, ABC transporters at the BBB hinder drug entry, presenting challenges for effective pharmacotherapy. Understanding the context-dependent changes in ABC transporter expression and function is crucial for elucidating the etiology and developing treatments for brain diseases.
三磷酸腺苷结合盒(ABC)转运蛋白促进多种分子在细胞膜内的运动,包括中枢神经系统内的分子。尽管这些转运蛋白在形成血脑屏障(BBB)的微血管内皮细胞中研究得最为广泛,但其他中枢神经系统细胞类型也表达这些转运蛋白。重要的是,疾病期间中枢神经系统微环境的破坏会改变转运蛋白的表达和功能。通过这项全面的综述,我们探讨了 ABC 转运蛋白在各种脑病理中的调节作用,以及这些变化的上下文相关后果。例如,ABCB1 的下调可能会加剧阿尔茨海默病中的淀粉样β斑块沉积,并促进帕金森病中神经毒性化合物的进入。上调可能会通过协助趋化因子介导的 CD8 T 细胞流入多发性硬化病变而加重神经炎症。总体而言,BBB 上的 ABC 转运蛋白会阻碍药物进入,这给有效的药物治疗带来了挑战。了解 ABC 转运蛋白表达和功能的上下文相关变化对于阐明脑疾病的病因和开发治疗方法至关重要。