Skip to main content
Log in

Effect of single-walled carbon nanotubes on primary immune cells in vitro

  • Research Article
  • Published:
Frontiers of Materials Science in China Aims and scope Submit manuscript

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 μg/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 μg/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 μg/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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Service R F. Nanomaterials show signs of toxicity. Science, 2003, 300(11): 243–245

    Article  Google Scholar 

  2. Kelly K L. Nanotechnology grows up. Science, 2004, 304: 1732–1734

    Article  Google Scholar 

  3. Brumfiel G A. Little knowledge. Nature, 2003, 424(17): 246–247

    Article  CAS  Google Scholar 

  4. Zhang W X. Environmental technologies at the nanoscale. Environmental Science & Technology, 2003, 37(5): 103–108

    Google Scholar 

  5. Wang B, Feng W Y, Zhao Y L, et al. Status of study on biological and toxicological effects of nanoscale materials. Science in China Ser. B: Chemistry, 2005, 48(5): 385–394

    Article  Google Scholar 

  6. Lam C W, James J T, McCluskey R, et al. Pulmonary toxicity of single-wall carbon nanotubes in mice 7 and 90 days after intratracheal instillation. Toxicology Science, 2004, 77(1): 126–134

    Article  CAS  Google Scholar 

  7. Zanello L P, Zhao B, Hu H, et al. Bone cell proliferation on carbon nanotubes. Nano Letters, 2006, 6(3): 562–567

    Article  CAS  Google Scholar 

  8. Zhang D W, Yi C Q, Zhang J C, et al. The effects of carbon nanotubes on the proliferation and differentiation of primary osteoblasts. Nanotechnology, 2007, 18: 475102 (9 pages)

    Google Scholar 

  9. Liu J, Andrew G R, Dai H J, et al. Fullerene pipes. Science, 1998, 280(5367): 1253–1256

    Article  CAS  Google Scholar 

  10. Ribeiro-Dias F, Barbuto J A M, Tsujita M, et al. Discrimination between NK and LAK cytotoxic activities of murine spleen cell by MTT assay: differential inhibition by PGE2 and EDTA. Journal of Immunological Methods, 2000, 241(1–2): 121–129

    Article  CAS  Google Scholar 

  11. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Journal of Immunological Methods, 1983, 65: 55–63

    Article  CAS  Google Scholar 

  12. Dumortier H, Lacotte S P, Giorgia P, et al. Functionalized carbon nanotubes are non-cytotoxic and preserve the functionality of primary immune cells. Nano Letters, 2006, 6(7): 1522–1528

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jin-chao Zhang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhang, Jc., Ji, Xy., Liu, Cl. et al. Effect of single-walled carbon nanotubes on primary immune cells in vitro . Front. Mater. Sci. China 2, 228–232 (2008). https://doi.org/10.1007/s11706-008-0038-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11706-008-0038-0

Keywords

Navigation