Priming and activation of mouse macrophages by trehalose 6,6'-dicorynomycolate vesicles from Corynebacterium glutamicum

FEMS Immunol Med Microbiol. 2002 Jan 14;32(2):141-7. doi: 10.1111/j.1574-695X.2002.tb00546.x.

Abstract

Vesicles consisting of pure trehalose dicorynomycolate (TDCM), the corynebacterial analog of the most studied mycobacterial glycolipid 'cord factor', were isolated from Corynebacterium glutamicum cells by mild detergent treatment; these induced in vivo a macrophage priming similar to that obtained with mycobacterial-derived trehalose dimycolate. In vitro, both TDCM and bacterial lipopolysaccharide (LPS) induced in macrophages the production of nitric oxide (NO) and tumor necrosis factor-alpha (TNF-alpha), endotoxin tolerance, and were primed for an enhanced secondary NO response to LPS. Interferon-gamma pretreatment did not influence the LPS-induced TNF-alpha response, but considerably increased the TDCM-induced response.

MeSH terms

  • Adjuvants, Immunologic*
  • Animals
  • Cells, Cultured
  • Cord Factors / immunology*
  • Cord Factors / isolation & purification
  • Corynebacterium / immunology*
  • Female
  • Macrophage Activation / immunology*
  • Macrophages, Peritoneal / cytology
  • Macrophages, Peritoneal / immunology*
  • Mice

Substances

  • Adjuvants, Immunologic
  • Cord Factors
  • 6,6'-dicorynomycolyl trehalose