Lymphocytes modulate peritoneal leukocyte recruitment in peritonitis

Inflamm Res. 2009 Sep;58(9):553-60. doi: 10.1007/s00011-009-0019-5. Epub 2009 Mar 5.

Abstract

Objective and design: To investigate the modulating role of lymphocytes in leukocyte recruitment in a murine model of peritonitis.

Materials or subjects: RAG-1 knockout (KO) mice, NUDE mice and microMT KO mice were compared to their wild-type controls.

Treatment: Mice were administered with 1 ml of Brewer's thioglycollate (BTG) and terminal peritoneal lavages were performed at 8, 24, 72 and 120 h after treatment.

Methods: Leukocyte numbers recruited at the different time points following a BTG administration were determined. Chemokine and cytokine levels were assessed by either ELISAs or cytometric bead array.

Results: RAG-1 KO mice (absent B and T cells) exhibited increased early neutrophil infiltration and blunted late monocyte/macrophage infiltration. NUDE mice (absent T cells) exhibited both increased neutrophil and monocyte/macrophage infiltration. In contrast, microMT KO mice (absent B cells) demonstrated reduced influx of both neutrophils and monocyte/macrophages. Chemokine analysis revealed various differences in important chemokines.

Conclusions: These data suggest that T cells act to suppress leukocyte recruitment while B cells promote leukocyte recruitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / immunology
  • Chemokines / immunology
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Leukocytes / cytology
  • Leukocytes / immunology*
  • Lymphocytes / cytology
  • Lymphocytes / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Nude
  • Peritoneum* / cytology
  • Peritoneum* / immunology
  • Peritonitis / immunology*
  • T-Lymphocytes / immunology

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Chemokines
  • Homeodomain Proteins
  • Interleukin-6
  • RAG-1 protein