Al-Omar Mohsen S, Jabir Majid, Karsh Esraa, Kadhim Rua, Sulaiman Ghassan M, Taqi Zainab J, Khashan Khawla S, Mohammed Hamdoon A, Khan Riaz A, Mohammed Salman A A
Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Qassim 51452, Saudi Arabia.
Medicinal Chemistry and Pharmacognosy Department, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Nanomaterials (Basel). 2021 May 24;11(6):1382. doi: 10.3390/nano11061382.
The study aimed to investigate the roles of gold nanoparticles (GNPs) and graphene oxide flakes (GOFs) as phagocytosis enhancers against cancer cells. The nanomaterials were characterized through SEM and UV-VIS absorptions. The GNPs and GOFs increased the macrophages' phagocytosis ability in engulfing, thereby annihilating the cancer cells in both in vitro and in vivo conditions. The GNPs and GOFs augmented serine protease class apoptotic protein, granzyme, passing through the aquaporin class protein, perforin, with mediated delivery through the cell membrane site for the programmed, calibrated, and conditioned cancer cells killing. Additionally, protease inhibitor 3,4-dichloroisocoumarin (DCI) significantly reduced granzyme and perforin activities of macrophages. The results demonstrated that the GOFs and GNPs increased the activation of phagocytic cells as a promising strategy for controlling cancer cells by augmenting the cell mortality through the granzyme-perforin-dependent mechanism.
该研究旨在调查金纳米颗粒(GNPs)和氧化石墨烯片(GOFs)作为吞噬作用增强剂对抗癌细胞的作用。通过扫描电子显微镜(SEM)和紫外可见吸收对这些纳米材料进行了表征。金纳米颗粒和氧化石墨烯片增强了巨噬细胞在吞噬过程中的吞噬能力,从而在体外和体内条件下消灭癌细胞。金纳米颗粒和氧化石墨烯片增加了丝氨酸蛋白酶类凋亡蛋白颗粒酶,通过水通道蛋白类蛋白穿孔素介导传递,通过细胞膜位点实现对程序化、校准化和条件化癌细胞的杀伤。此外,蛋白酶抑制剂3,4-二氯异香豆素(DCI)显著降低了巨噬细胞的颗粒酶和穿孔素活性。结果表明,氧化石墨烯片和金纳米颗粒通过颗粒酶-穿孔素依赖性机制增加细胞死亡率,增强吞噬细胞的激活,是一种控制癌细胞的有前景的策略。