Orzechowska Beata U, Kukowska-Latallo Jolanta F, Coulter Alexa D, Szabo Zsuzsanna, Gamian Andrzej, Myc Andrzej
Department of Immunology of Infectious Diseases, Laboratory of Virology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.
Michigan Nanotechnology Institute for Medicine and Biological Sciences, University of Michigan Medical School, Ann Arbor, MI, United States.
Vaccine. 2015 May 5;33(19):2289-2296. doi: 10.1016/j.vaccine.2015.03.002. Epub 2015 Mar 25.
Nanoemulsions (NEs) are adjuvants that enhance antigen penetration of the nasal mucosa, increase cellular uptake of antigens by both epithelial and dendritic cells, and promote the migration of antigen-loaded dendritic cells to regional lymph nodes within 24-h of vaccine administration. The objective of this study was to elucidate cell death caused by W805EC NE and identify caspases and genes associated with death pathways. Consistent with this aim, we show that exposure of human epithelial cells (EC), both RPMI 2650 and FaDu, to NE results in the activation of caspases (1, 3/7, 6, 8, and 9) and the expression of genes involved in apoptotic as well as authophagy and necrosis pathways. Interestingly, the NE activates caspase 8 which promotes "immunogenic apoptosis". The rescue assay was employed to investigate the fate of RPMI 2650 cells treated with W805EC NE. After four-hour treatment with as little as 0.03% of NE no cells were rescued at 72h. Remarkably, immediately after four-hour treatment, the cells morphologically resembled untreated cells and most of the cells were alive. Altogether, these results suggest that NE induces death of human ECs through multiple pathways. Epithelial cell death caused by W805EC may have further implications on antigen uptake, processing, and presentation by DC's.
纳米乳剂(NEs)是一种佐剂,可增强鼻黏膜对抗原的渗透,增加上皮细胞和树突状细胞对抗原的摄取,并在疫苗接种后24小时内促进负载抗原的树突状细胞向局部淋巴结迁移。本研究的目的是阐明W805EC纳米乳剂引起的细胞死亡,并确定与死亡途径相关的半胱天冬酶和基因。与此目标一致,我们发现,将人上皮细胞(EC),即RPMI 2650细胞和FaDu细胞,暴露于纳米乳剂会导致半胱天冬酶(1、3/7、6、8和9)的激活以及参与凋亡、自噬和坏死途径的基因表达。有趣的是,纳米乳剂激活了促进“免疫原性凋亡”的半胱天冬酶8。采用挽救试验来研究用W805EC纳米乳剂处理的RPMI 2650细胞的命运。用低至0.03%的纳米乳剂处理4小时后,72小时时没有细胞被挽救。值得注意的是,在4小时处理后立即观察,细胞形态与未处理的细胞相似,并且大多数细胞是存活的。总之,这些结果表明纳米乳剂通过多种途径诱导人上皮细胞死亡。W805EC引起的上皮细胞死亡可能对抗原摄取、处理以及树突状细胞的呈递产生进一步影响。