Cyclic stretching of mesangial cells up-regulates intercellular adhesion molecule-1 and leukocyte adherence: a

B L Riser1, J Varani, P Cortes

  • 1Department of Medicine, Division of Nephrology and Hypertension, Henry Ford Hospital, Detroit, MI 48202, USA. riserb@usa.net

Insights

Intraglomerular hypertension increases mesangial cell intercellular adhesion molecule-1 (ICAM-1), promoting leukocyte adherence. This finding links hypertension to inflammation and glomerulosclerosis in kidney diseases.

Area of Science:

  • Nephrology
  • Cell Biology
  • Pathophysiology

Background:

  • Intraglomerular hypertension drives glomerulosclerosis in diabetic nephropathy and renal ablation.
  • Glomerular mesangial cell (MC) inflammation and MC/leukocyte interactions are implicated in kidney diseases.
  • Intercellular adhesion molecule-1 (ICAM-1) mediates MC/leukocyte interactions in glomerulonephritis.

Purpose of the Study:

  • To investigate if cyclic stretching of mesangial cells up-regulates ICAM-1 expression and activity.
  • To determine the relationship between mechanical stretch and inflammatory responses in mesangial cells.

Main Methods:

  • Cultured mesangial cells were subjected to cyclic stretching.
  • ICAM-1 mRNA and protein levels were measured.
  • Leukocyte adherence to stretched mesangial cells was quantified.
  • Effects of tumor necrosis factor-alpha (TNF-α) were compared.

Main Results:

  • Cyclic stretching significantly increased mesangial cell ICAM-1 mRNA and protein levels in a dose- and time-dependent manner.
  • Stretch-induced ICAM-1 led to increased phagocytic leukocyte adherence, comparable to TNF-α.
  • Combined stretch and TNF-α resulted in an additive increase in leukocyte adherence.

Conclusions:

  • Mechanical stretch is a potent stimulus for ICAM-1 expression in mesangial cells.
  • Stretch-induced ICAM-1 provides a direct link between intraglomerular hypertension and inflammation.
  • This mechanism contributes to glomerulosclerosis progression in various kidney diseases.

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