Existence of a regulatory loop between MCP-1 and TGF-beta in glomerular immune injury

Am J Physiol Renal Physiol. 2002 Nov;283(5):F1075-84. doi: 10.1152/ajprenal.00349.2001.

Abstract

Glomerular upregulation of monocyte chemotactic protein-1 (MCP-1), followed by an influx of monocytes resulting eventually in extracellular matrix deposition is a common sequel of many types of glomerulonephritis. However, it is not entirely clear how early expression of MCP-1 is linked to the later development of glomerulosclerosis. Because transforming growth factor-beta (TGF-beta) is a key regulator of extracellular matrix proteins, we hypothesized that there might be a regulatory loop between early glomerular MCP-1 induction and subsequent TGF-beta expression. To avoid interference with other cytokines that may be released from infiltrating monocytes, isolated rat kidneys were perfused with a polyclonal anti-thymocyte-1 antiserum (ATS) and rat serum (RS) as a complement source to induce glomerular injury. Renal TGF-beta protein and mRNA expressions were strongly stimulated after perfusion with ATS-RS. This effect was attenuated by coperfusion with a neutralizing anti-MCP-1 but was partly mimicked by perfusion with recombinant MCP-1 protein. On the other hand, renal MCP-1 expression and production were stimulated by administration of ATS-RS. Additional perfusion with an anti-TGF-beta antibody further aggravated this increase, whereas application of recombinant TGF-beta protein reduced MCP-1 formation. Our data demonstrate an intrinsic regulatory loop in which increased MCP-1 levels stimulate TGF-beta formation in resident glomerular cells in the absence of infiltrating immune competent cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism*
  • Extracellular Matrix / immunology
  • Extracellular Matrix / metabolism
  • Gene Expression / physiology
  • Glomerulonephritis / immunology*
  • Glomerulonephritis / metabolism*
  • In Vitro Techniques
  • Kidney / metabolism
  • Male
  • RNA, Messenger / analysis
  • Rats
  • Rats, Wistar
  • Receptors, CCR2
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism*
  • Urine

Substances

  • Ccr2 protein, rat
  • Chemokine CCL2
  • RNA, Messenger
  • Receptors, CCR2
  • Receptors, Chemokine
  • Transforming Growth Factor beta