Pleskova Svetlana N, Mikheeva Elza R, Gornostaeva Ekaterina E
Lobachevsky State University of Nizhny Novgorod, 23 Gagarin Ave., Build 3, 208, Nizhny Novgorod, 603950 Russia.
Lobachevsky State University of Nizhny Novgorod, 23 Gagarin Ave., Build 3, 208, Nizhny Novgorod, 603950 Russia.
Micron. 2018 Feb;105:82-92. doi: 10.1016/j.micron.2017.11.011. Epub 2017 Nov 23.
For biomedical applications, it is important to know, which kinds of blood cells can capture quantum dots (QDs). The maximum accumulation of QDs was found for the monocyte fraction of leukocytes, the minimum binding of QDs was observed for lymphocytes. It was found that CdSe/ZnS-MPA QDs are actively absorbed by the cells and have more expressed toxicity. The classical mechanism of the phagocytosis of QDs was revealed for neutrophils, when the QDs are located in phagolysosomes. The capture of QDs by neutrophil granulocytes has resulted in a destruction of certain types of QDs. The interaction of the neutrophils with the QDs has resulted in the death of the cells by one of the following cell death mechanisms: necrosis, apoptosis, autophagy, NETos, or mummification. The aggregation of the QDs manifested as an increase of the hydrodynamic diameter of the QDs was found to occur under the influence of serum and under the influence of blood cells (lymphocytes and neutrophils) in a serum-free medium.
对于生物医学应用而言,了解哪些类型的血细胞能够捕获量子点(QDs)至关重要。研究发现,白细胞中的单核细胞部分对量子点的积累量最大,而淋巴细胞对量子点的结合量最小。研究还发现,CdSe/ZnS-MPA量子点能被细胞积极吸收且具有更强的毒性。当中性粒细胞将量子点定位在吞噬溶酶体中时,揭示了量子点吞噬的经典机制。中性粒细胞对量子点的捕获导致了某些类型量子点的破坏。中性粒细胞与量子点的相互作用通过以下细胞死亡机制之一导致细胞死亡:坏死、凋亡、自噬、中性粒细胞胞外诱捕网(NETos)或木乃伊化。在血清的影响下以及在无血清培养基中血细胞(淋巴细胞和中性粒细胞)的影响下,发现量子点的聚集表现为量子点流体动力学直径的增加。