[Response of mouse macrophage cell line infected with Bacille Calmette-Guerin in vitro]

Wei Sheng Wu Xue Bao. 2010 Mar;50(3):373-9.
[Article in Chinese]

Abstract

Objective: To illuminate the response of mouse macrophage cell line RAW264.7 after infected with Bacille Calmette-Guerin (BCG) in vitro.

Methods: We analyzed the morphology and expression of co-stimulatory molecules on the surface of RAW264. 7 after exposure to BCG for 23 hours. Then during the different culture time after discard the BCG in the supernatant, we analyzed the response of RAW264. 7 by flow cytometry using carboxyfluorescein diacetate, succinimidyl ester (CFDA-SE), annexin V/PI and Rhodamine 123, respectively.

Results: We observed the phagosome containing BCG under transmission electronic microscope and RAW264. 7 cells still grow well after incubated with BCG for 23 hours. We found that the expression level of co-stimulatory molecules, CD40, CD54, CD80, CD86 and CD11b, were elevated evidently, except CD11c, I-A(d) and H-2K(d). The fluorescence intensity of BCG stained with CFDA-SE decreased with the prolongation of culture time, but it was still more higher than unstained control four days later. After removal of uninfected BCG, the percents of BCG-infected cell decreased and we didn't detected BCG-infected cells evidently for 60 h culture. Furthermore, we also found that there was no obvious cell apoptosis for all the time, and the mitochondrial membrane potential of BCG-infected cells increased early and then decreased to the same level as the uninfected control.

Conclusion: These results would be helpful to elucidate the mechanism of BCG vaccination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B7-1 Antigen / metabolism
  • B7-2 Antigen / metabolism
  • CD11b Antigen / metabolism
  • CD40 Antigens / metabolism
  • Cell Line
  • Flow Cytometry
  • Fluoresceins
  • Intercellular Adhesion Molecule-1 / metabolism
  • Macrophages / metabolism*
  • Macrophages / microbiology*
  • Macrophages / ultrastructure
  • Membrane Potential, Mitochondrial
  • Mice
  • Mice, Inbred BALB C
  • Microscopy
  • Microscopy, Electron, Transmission
  • Mycobacterium bovis / growth & development*
  • Mycobacterium bovis / physiology
  • Mycobacterium bovis / ultrastructure
  • Phagosomes / ultrastructure
  • Rhodamine 123
  • Succinimides

Substances

  • 5-(6)-carboxyfluorescein diacetate succinimidyl ester
  • B7-1 Antigen
  • B7-2 Antigen
  • CD11b Antigen
  • CD40 Antigens
  • Fluoresceins
  • Succinimides
  • Intercellular Adhesion Molecule-1
  • Rhodamine 123