Lipopolysaccharide-binding protein: localization in secretory granules of Paneth cells in the mouse small intestine

Histochem Cell Biol. 2009 Jun;131(6):727-32. doi: 10.1007/s00418-009-0572-6. Epub 2009 Feb 21.

Abstract

Lipopolysaccharide (LPS)-binding protein (LBP) is an acute-phase protein involved in the host's response to endotoxin and mainly synthesized and secreted to the blood by the liver. But in addition, LBP is also made by extrahepatic cells, including the enterocyte-like cell line Caco-2. To study in closer detail the synthesis and storage of LBP in the intestinal mucosal epithelium, we performed an immunolocalization of LBP in mouse small intestine. By immunofluorescence microscopy, an antibody recognizing the 58-60 kDa protein of LBP distinctly labeled a small population of cells located deep into the crypts. This cell population was also positive for lysozyme and alpha-defensin 4, identifying Paneth cells as the main intestinal LBP-producing cells. By immunogold electron microscopy, intense labeling was observed in the secretory granules of these cells. We conclude that Paneth cells express LBP together with other proteins acting in the innate immune response of the gut, such as lysozyme, defensins and intelectin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / metabolism*
  • Animals
  • Caco-2 Cells
  • Carrier Proteins / metabolism*
  • Cell Line, Tumor
  • Humans
  • Intestine, Small / metabolism*
  • Intestine, Small / ultrastructure
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Microscopy, Immunoelectron
  • Muramidase / metabolism
  • Paneth Cells / metabolism*
  • Paneth Cells / ultrastructure
  • Secretory Vesicles / metabolism*
  • Secretory Vesicles / ultrastructure
  • alpha-Defensins / metabolism

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • Membrane Glycoproteins
  • alpha-Defensins
  • lipopolysaccharide-binding protein
  • Muramidase