Effect of single-walled carbon nanotubes on primary
immune cells
ZHANG Jin-chao1, JI Xiao-yu1, LIU Cui-lian1, SHEN Shi-gang1, WANG Shu-xiang1, SUN Jing2
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1.College of Chemistry and Environmental Science, Hebei University;Chemical Biology Laboratory, Hebei University; 2.B-Ultrasound Room, Affiliated Hospital of Hebei University
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Published
05 Jun 2008
Issue Date
05 Jun 2008
Abstract
Carbon nanotubes (CNTs) are emerging as innovative tools in nanobiotechnology. However, their toxic effects on environment and health have become an issue of great concern. The effect of single-walled carbon nanotubes (SWCNTs) on primary immune cells in vitro was studied in this paper. The results indicated that SWCNTs (25 and 50 ?g/mL) could promote the proliferation of spleen cells. However, they had no significant effect on the proliferation of spleen cells at concentrations of 1 and 10 ?g/mL. They also had no effect on T-lymphocyte proliferation stimulated by concanavalinA (ConA) at lower concentrations. Moreover, they turned to inhibit T-lymphocyte proliferation at higher concentrations. It was found that SWCNTs inhibited the B-lymphocyte proliferation stimulated by lipopolysaccharides (LPS) at concentrations of 1, 10, 25 and 50 ?g/mL. What is more, they significantly decreased the Natural Killer (NK) cell activity compared with the control group at all tested concentrations. The results suggest that SWCNTs have possibly negative effects on immune cells in vitro.
ZHANG Jin-chao, JI Xiao-yu, LIU Cui-lian, SHEN Shi-gang, WANG Shu-xiang, SUN Jing.
Effect of single-walled carbon nanotubes on primary
immune cells. Front. Mater. Sci., 2008, 2(2): 228‒232 https://doi.org/10.1007/s11706-008-0038-0
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References
1. Service R F Nanomaterialsshow signs of toxicityScience 2003 300(11)243245. doi:10.1126/science.300.5617.243a 2. Kelly K L Nanotechnologygrows upScience 2004 30417321734. doi:10.1126/science.304.5678.1732 3. Brumfiel G A LittleknowledgeNature 2003 424(17)246247. doi:10.1038/424246a 4. Zhang W X Environmentaltechnologies at the nanoscaleEnvironmentalScience & Technology 2003 37(5)103108 5. Wang B Feng W Y Zhao Y L et al.Status of study on biological and toxicologicaleffects of nanoscale materialsScience inChina Ser. B: Chemistry 2005 48(5)385394. doi:10.1360/042004‐26 6. Lam C W James J T McCluskey R et al.Pulmonary toxicity of single-wall carbon nanotubesin mice 7 and 90 days after intratracheal instillationToxicology Science 2004 77(1)126134. doi:10.1093/toxsci/kfg243 7. Zanello L P Zhao B Hu H et al.Bone cell proliferation on carbon nanotubesNano Letters 2006 6(3)562567. doi:10.1021/nl051861e 8. Zhang D W Yi C Q Zhang J C et al.The effects of carbon nanotubes on the proliferationand differentiation of primary osteoblastsNanotechnology 2007 18475102(9 pages) 9. Liu J Andrew G R Dai H J et al.Fullerene pipesScience 1998 280(5367)12531256. doi:10.1126/science.280.5367.1253 10. Ribeiro-Dias F Barbuto J A M Tsujita M et al.Discrimination between NK and LAK cytotoxic activitiesof murine spleen cell by MTT assay: differential inhibition by PGE2 and EDTAJournal of ImmunologicalMethods 2000 241(1–2)121129. doi:10.1016/S0022‐1759(00)00206‐4 11. Mosmann T Rapidcolorimetric assay for cellular growth and survival: application toproliferation and cytotoxicity assaysJournalof Immunological Methods 1983 655563. doi:10.1016/0022‐1759(83)90303‐4 12. Dumortier H Lacotte S P Giorgia P et al.Functionalized carbon nanotubes are non-cytotoxicand preserve the functionality of primary immune cellsNano Letters 2006 6(7)15221528. doi:10.1021/nl061160x
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