Inhibition of bfl-1/A1 by siRNA inhibits mycobacterial growth in THP-1 cells by enhancing phagosomal acidification

Biochim Biophys Acta. 2008 Apr;1780(4):733-42. doi: 10.1016/j.bbagen.2007.12.010. Epub 2008 Jan 16.

Abstract

Virulent tubercle bacilli inhibit apoptosis to establish a safe environment within the host cells. Here, we report that NF-kappaB dependent antiapoptotic protein bfl-1/A1 plays an important role in this process. Both virulent and avirulent mycobacteria bearing THP-1 cells expressed considerable amount of bfl-1/A1 after 4 h of infection. However, after 48 h of infection, bfl-1/A1 expression was evident only in Mycobacterium tuberculosis H37Rv but not in M. tuberculosis H37Ra infected cells. When parallel experiments were performed with Human monocyte-derived macrophages (MDMs), differential expression of bfl-1/A1 mRNA was observed in case of M. tuberculosis H37Rv and M. tuberculosis H37Ra infection. siRNA mediated inhibition of bfl-1/A1 induced apoptosis in M. tuberculosis H37Rv infected THP-1 and MDMs. Reduction in intracellular mycobacterial growth was observed in bfl-1/A1 siRNA transfected, M. tuberculosis H37Rv infected THP-1 cells. Enhancement of phagosome-lysosome fusion was observed in bfl-1/A1 siRNA treated and M. tuberculosis H37Rv infected THP-1 cells. These results clearly indicated that differential expression of bfl-1/A1 in M. tuberculosis H37Rv and M. tuberculosis H37Ra infected THP-1 cells probably account for the difference in infection outcome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acids / chemistry
  • Apoptosis
  • Blotting, Western
  • Caspase 3 / metabolism
  • Cell Line
  • Cells, Cultured
  • Green Fluorescent Proteins / chemistry
  • Humans
  • Hydrogen-Ion Concentration
  • Intracellular Space / microbiology
  • Luciferases / genetics
  • Luciferases / metabolism
  • Macrophages / cytology
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Microscopy, Confocal
  • Minor Histocompatibility Antigens
  • Monocytes / cytology
  • Monocytes / metabolism*
  • Monocytes / microbiology
  • Mycobacterium tuberculosis / chemistry
  • Mycobacterium tuberculosis / growth & development*
  • Phagosomes / chemistry
  • Phagosomes / metabolism*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • RNA Interference
  • RNA, Small Interfering / genetics*
  • Reactive Oxygen Species / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transfection

Substances

  • Acids
  • BCL2-related protein A1
  • Minor Histocompatibility Antigens
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • Luciferases
  • Caspase 3