Activation of human neutrophils by Arg‐Gly‐Asp‐Ser immobilized on microspheres

Yuji Kasuya, Keiji Fujimoto, Masaki Miyamoto, Haruma Kawaguchi

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The adhesive interaction of cells with extracellular matrix components is essential for a variety of cellular functions, and is frequently mediated by a tetra peptide, Arg‐Gly‐Asp‐Ser (RGDS), located within fibronectin and other proteins. In this study, the RGDS‐mediated activation of polymorphonuclear leukocytes accompanied by phagocytosis was investigated using monodisperse polymeric microspheres carrying RGDS. The parent and Arg‐Gly‐Glu‐Ser (RGES)‐carrying microspheres, which have no adhesion activity, were employed as controls. The ingestion of microspheres into PMN was not enhanced by immobilizing RGDS. However, PMNs exhibited unique oxygen consumption and enhanced liberation of reactive oxygen when RGDS‐carrying microspheres were phagocytosed. These PMN responses disappeared with the addition of soluble RGDS. Furthermore, cytochalasin D, which inhibits actin polymerization, showed a marked inhibitory effect on oxygen consumption in the RGDS‐carrying microsphere system, as compared with those in other systems. These findings show that RGDS‐carrying microspheres induced the biospecific activation of PMNs by the signal transduction via RGDS‐integrin binding without alteration in the degree of phagocytosis. © 1994 John Wiley & Sons, Inc.

Original languageEnglish
Pages (from-to)397-404
Number of pages8
JournalJournal of Biomedical Materials Research
Volume28
Issue number3
DOIs
Publication statusPublished - 1994 Mar

ASJC Scopus subject areas

  • Biomaterials
  • Biomedical Engineering

Fingerprint Dive into the research topics of 'Activation of human neutrophils by Arg‐Gly‐Asp‐Ser immobilized on microspheres'. Together they form a unique fingerprint.

  • Cite this