Are murine marginal-zone macrophages the splenic white pulp analog of high endothelial venules?

Eur J Immunol. 1995 Nov;25(11):3165-72. doi: 10.1002/eji.1830251127.

Abstract

The entry of lymphocytes into the spleen, in contrast to lymph nodes, does not involve high endothelial venule (HEV) interaction. The precise point of entry, as well as the mechanism by which lymphocytes enter the lymphoid areas of the spleen, remains controversial. We examined in detail the effect of two agents, pertussis toxin (PT) and the sulfated polysaccharide fucoidan, on splenic lymphocyte entry and positioning. These have previously been shown to interfere with lymphocyte extravasation across HEV. PT prevents lymphocyte extravasation, but not binding, to HEV, whereas fucoidan prevents binding and thus subsequent extravasation. Studies presented here show that pretreatment of murine lymphocytes with PT does not numerically affect entry into spleen, but profoundly alters lymphocyte positioning within the spleen. When fluorescently labeled, PT-treated lymphocytes are injected intravenously, they initially accumulate in the marginal zone, in apparent association with the layer of marginal zone macrophages (MZM phi) which form a shell around the white pulp. They fail to traverse this layer into the white pulp, and subsequently localize in the red pulp. In contrast, untreated cells initially appear in the marginal zone, then continue to migrate into the white pulp after traversing the MZM phi layer. The localization of PT-pretreated lymphocytes adjacent to the MZM phi layer is disrupted by intravenous administration of fucoidan. Using a flow cytometric assay of aggregation between MZM phi and lymphocytes, we confirmed that fucoidan is also able to inhibit this association in vitro, whereas PT has no effect on this interaction. We propose that MZM phi in the mouse are the splenic analog of HEV, forming the port of entry of lymphocytes into the white pulp of the spleen.

MeSH terms

  • Animals
  • Cell Adhesion / drug effects
  • Cell Movement / drug effects*
  • Endothelium, Vascular / physiology*
  • Female
  • Lymphocytes / drug effects
  • Macrophages / cytology*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Pertussis Toxin
  • Polysaccharides / toxicity
  • Receptors, Lymphocyte Homing / drug effects
  • Spleen / cytology*
  • Spleen / drug effects
  • Virulence Factors, Bordetella / toxicity

Substances

  • Polysaccharides
  • Receptors, Lymphocyte Homing
  • Virulence Factors, Bordetella
  • fucoidan
  • Pertussis Toxin