Department of Chemistry, University of Rome La Sapienza, Piazzale A. Moro 5, 00185, Rome, Italy.
Department of Environmental Biology, University of Rome La Sapienza, Piazzale A. Moro 5, 00185, Rome, Italy.
Plant Cell Rep. 2017 Dec;36(12):1917-1928. doi: 10.1007/s00299-017-2206-0. Epub 2017 Sep 14.
PLGA NPs' cell uptake involves different endocytic pathways. Clathrin-independent endocytosis is the main internalization route. The cell wall plays a more prominent role than the plasma membrane in NPs' size selection. In the last years, many studies on absorption and cell uptake of nanoparticles by plants have been conducted, but the understanding of the internalization mechanisms is still largely unknown. In this study, polydispersed and monodispersed poly(lactic-co-glycolic) acid nanoparticles (PLGA NPs) were synthesized, and a strategy combining the use of transmission electron microscopy (TEM), confocal analysis, fluorescently labeled PLGA NPs, a probe for endocytic vesicles (FM4-64), and endocytosis inhibitors (i.e., wortmannin, ikarugamycin, and salicylic acid) was employed to shed light on PLGA NP cell uptake in grapevine cultured cells and to assess the role of the cell wall and plasma membrane in size selection of PLGA NPs. The ability of PLGA NPs to cross the cell wall and membrane was confirmed by TEM and fluorescence microscopy. A strong adhesion of PLGA NPs to the outer side of the cell wall was observed, presumably due to electrostatic interactions. Confocal microscopy and treatment with endocytosis inhibitors suggested the involvement of both clathrin-dependent and clathrin-independent endocytosis in cell uptake of PLGA NPs and the latter appeared to be the main internalization pathway. Experiments on grapevine protoplasts revealed that the cell wall plays a more prominent role than the plasma membrane in size selection of PLGA NPs. While the cell wall prevents the uptake of PLGA NPs with diameters over 50 nm, the plasma membrane can be crossed by PLGA NPs with a diameter of 500-600 nm.
PLGA NPs 的细胞摄取涉及不同的内吞途径。网格蛋白非依赖内吞作用是主要的内化途径。细胞壁在纳米颗粒的尺寸选择中比质膜起着更为突出的作用。在过去的几年中,已经有许多关于植物对纳米颗粒吸收和细胞摄取的研究,但对内化机制的理解仍知之甚少。在这项研究中,合成了多分散和单分散的聚(乳酸-共-乙醇酸)纳米颗粒(PLGA NPs),并结合使用透射电子显微镜(TEM)、共聚焦分析、荧光标记的 PLGA NPs、内吞小泡探针(FM4-64)和内吞抑制剂(即wortmannin、ikarugamycin 和水杨酸)的策略,阐明了 PLGA NP 在葡萄培养细胞中的摄取机制,并评估了细胞壁和质膜在 PLGA NP 尺寸选择中的作用。通过 TEM 和荧光显微镜证实了 PLGA NPs 穿过细胞壁和细胞膜的能力。观察到 PLGA NPs 强烈附着在细胞壁的外侧,这可能是由于静电相互作用。共聚焦显微镜和内吞抑制剂处理表明,CLATHRIN 依赖性和 CLATHRIN 非依赖性内吞作用都参与了 PLGA NPs 的细胞摄取,后者似乎是主要的内化途径。对葡萄原生质体的实验表明,细胞壁在 PLGA NPs 的尺寸选择中比质膜起着更为突出的作用。虽然细胞壁阻止了直径超过 50nm 的 PLGA NPs 的摄取,但直径为 500-600nm 的 PLGA NPs 可以穿过质膜。