School of Pharmacy, University of Nottingham, University Park, Nottingham NG7 2RD, U.K.
School of Cancer & Pharmaceutical Sciences, Faculty of Life Sciences & Medicine, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, U.K.
Mol Pharm. 2024 Jul 1;21(7):3603-3612. doi: 10.1021/acs.molpharmaceut.4c00333. Epub 2024 Jun 12.
Understanding the internalization of nanosized particles by mucosal epithelial cells is essential in a number of areas including viral entry at mucosal surfaces, nanoplastic pollution, as well as design and development of nanotechnology-type medicines. Here, we report our comparative study on pathways of cellular internalization in epithelial Caco-2 cells cultured in vitro as either a polarized, differentiated cell layer or as nonpolarized, nondifferentiated cells. The study reveals a number of differences in the extent that endocytic processes are used by cells, depending on their differentiation status and the nature of applied nanoparticles. In , actin-driven and dynamin-independent macropinocytosis plays a prominent role in the internalization of both positively and negatively charged nanoparticles, contrary to its modest contribution in nonpolarized cells. Clathrin-mediated cellular entry plays a prominent role in the endocytosis of positive nanoparticles and cholesterol inhibition in negative nanoparticles. However, in dynamin-dependent endocytosis is a major pathway in the internalization of both positive and negative nanoparticles. Cholesterol depletion affects both nonpolarized and polarized cells' internalization of positive and negative nanoparticles, which, in addition to the effect of cholesterol-binding inhibitors on the internalization of negative nanoparticles, indicates the importance of membrane cholesterol in endocytosis. The data collectively provide a new contribution to understanding endocytic pathways in epithelial cells, particularly pointing to the importance of the cell differentiation stage and the nature of the cargo.
了解黏膜上皮细胞对纳米颗粒的内化作用对于许多领域都至关重要,包括黏膜表面的病毒进入、纳米塑料污染,以及纳米技术药物的设计和开发。在这里,我们报告了一项关于体外培养的上皮细胞 Caco-2 细胞内化途径的比较研究,这些细胞分别处于极化分化和非极化非分化状态。研究揭示了细胞根据其分化状态和应用的纳米颗粒性质,在多大程度上利用内吞作用的差异。在分化细胞中,肌动蛋白驱动的、与网格蛋白无关的巨胞饮作用在正电荷和负电荷纳米颗粒的内化中起着重要作用,而在非极化细胞中其作用较小。网格蛋白介导的细胞内吞作用在正电荷纳米颗粒的内化中起着重要作用,而胆固醇抑制作用则在负电荷纳米颗粒中起作用。然而,在非极化细胞和极化细胞中,动力蛋白依赖性内吞作用是正电荷和负电荷纳米颗粒内化的主要途径。胆固醇耗竭会影响正电荷和负电荷纳米颗粒在非极化和极化细胞中的内化,除了胆固醇结合抑制剂对负电荷纳米颗粒内化的影响外,这表明膜胆固醇在内吞作用中的重要性。这些数据为理解上皮细胞的内吞途径提供了新的贡献,特别是指出了细胞分化阶段和货物性质的重要性。