Intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) expression and function on cultured human glomerular epithelial cells

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Abstract
SUMMARY: Glomerular epithelial cells are involved in extracapillary inflammation (crescents) but the mechanisms of this extracapillary accumulation of macrophages, epithelial cells and occasional lymphocytes are unknown. Human glomerular parietal epithelial cells express ICAM-1 and VCAM-1 on immunohistological stains of renal biopsies. We studied the expression of these cell adhesion molecules on cultured human glomerular epithelial cells (HGEC), their regulation by pro-inflammatory cytokines, and their role in mediating the adhesion of concanavalin A (Con A)-activated peripheral blood mononuclear cells. Human glomerular epithelial cells in culture constitutively express ICAM-1 and VCAM-1. The expression of ICAM-1 was not significantly altered by tumour necrosis factor-alpha (TNF-α) (P= 0·32), IL-β (P= 0·24), interferon-gamma (IFN-γ) (P=0·66) or IL-4 (P = 0·85). VCAM-1 expression was increased by all four cytokines, but only significantly so by IL-4 (P= 0·0001). Con A-stimulated, monocyte-depleted peripheral blood lymphocytes bound to human glomerular epithelial cells, median 28·9% (range 14·5–37·9%). This adherence was significantly inhibited by anti-ICAM-1 (P=0·03) and anti-LFA-1 (P=0·02), but not by anti-VCAM-1 (P= 0·13) or by antibody to von Willebrand factor (P= NS). The interaction between ICAM-1 on HGEC and LFA-1 on mononuclear cells may be important in the pathogenesis of extracapillary inflammation in glomerulonephritis.