Glucose-induced changes in integrins and matrix-related functions in cultured human glomerular epithelial cells

Paraskevi V. Kitsiou, Athina K. Tzinia, William G. Stetler-Stevenson, Alfred F. Michael, Wei Wei Fan, Bing Zhou, Effie C. Tsilibary

Research output: Contribution to journalArticlepeer-review

72 Scopus citations

Abstract

In cultured human glomerular epithelial cells (HGEC), 25 mM glucose resulted in decreased expression of α3-, α2-, and β1-integrins and increased expression of α5- and αvβ3-integrins. This change was accompanied by decreased binding of HGEC to type IV collagen. In the presence of normal (5 mM) glucose concentration, cell binding to type IV collagen was primarily mediated by α2β1- and α5β1-integrins, as indicated by experiments in which cell adhesion to type IV collagen was competed by specific anti-integrin monoclonal antibodies. In the presence of high (25 mM) glucose, the upregulated α5and αaβ3-integrins were mainly involved in cell binding to type IV collagen. Furthermore, high glucose decreased expression of matrix metalloproteinase-2 (MMP-2), a collagenase regulated in part by α3β1-integrin, as suggested by the use of ligand-mimicking antibodies against these integrins, which resulted in release of increased amounts of MMP-2 in the culture medium. Finally, tissue inhibitor of metalloproteinase-2, the specific inhibitor of MMP-2, was upregulated in high glucose and could contribute to matrix accumulation. These changes could help explain basement membrane thickening in diabetes.

Original languageEnglish (US)
Pages (from-to)F671-F679
JournalAmerican Journal of Physiology - Renal Physiology
Volume284
Issue number4 53-4
DOIs
StatePublished - Apr 1 2003

Keywords

  • Diabetes
  • Matrixins
  • Signaling
  • Tissue inhibitors of metalloproteinases

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