4.7 Article

Irsogladine maleate regulates neutrophil migration and E-cadherin expression in gingival epithelium stimulated by Aggregatibacter actinomycetemcomitans

Journal

BIOCHEMICAL PHARMACOLOGY
Volume 79, Issue 10, Pages 1496-1505

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2010.01.017

Keywords

Irsogladine maleate; Aggregatibacter actinomycetemcomitans; E-cadherin; Neutrophil migration; CXC-chemokine; Gingival epithelial cells

Funding

  1. Japan Society for the Promotion of Science, Japan [20791613]
  2. Grants-in-Aid for Scientific Research [20791613] Funding Source: KAKEN

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Irsogladine maleate (IM) counters Aggregatibacter actinomycetemcomitans-induced reduction of the gap junction intercellular communication and the expression of zonula occludens-1, which is a major tight junction structured protein, in cultured human gingival epithelial cells (HGEC) In addition, IM obviates the A actinomycetemcomitans-induced increase in interleukin (IL)-8 levels in HGEC Thus, by regulating the intercellular junctional complex and chemokine secretion in HGEC, IM may be useful to prevent periodontal disease. To clarify the effects and regulatory mechanism of IM in vivo and in vitro, we examined the expression of E-cadherin and neutrophil chemotaxis induced by A actinomycetemcomitans under IM pretreatment Immunohistochemical studies revealed that A actinomycetemcomitans application to the gingival sulcus decreased the number of cells positive for E-cadherin and increased those positive for cytokine-induced neutrophil chemoattractant-2 alpha (CINC-2 alpha) in rat gingival epithelium. However, in IM-pretreated rats, A actinomycetemcomitans application had little effect on CINC-2 alpha and E-cadherin in gingival epithelium In cultured HGEC, real-time PCR and Western blotting showed that IM and the ERK inhibitor PD98059 abolished the A actinomycetemcomitans-induced increase in CXCL-1 and IL-8 in HGEC On the other hand, IM, PD98059, and the p38 MAP kinase inhibitor SB203580 recovered the decrease in E-cadherin expression In addition, conditioned medium from A actinomycetemcomitans-stimulated HGEC enhanced human neutrophil chemotaxis, compared to that from un-stimulated HGEC or that from A actinomycetemcomitans-stimulated HGEC under IM pretreatment. Furthermore, IM down-regulated the p38 MAP kinase and ERK phosphorylations induced by A actinomycetemcomitans In conclusion, IM may control A. actinomycetemcomitans-induced gingival inflammation by regulating neutrophil migration and E-cadherin expression in gingival epithelium (C) 2010 Elsevier Inc All rights reserved

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