Decay-accelerating factor is expressed is the human endometrium and may serve as the attachment ligand for Dr pili of Escherichia coli

  • A. Kaul
  • , B. J. Nowicki
  • , M. G. Martens
  • , P. Goluszko
  • , A. Hart
  • , M. Nagamani
  • , D. Kumar
  • , T. Q. Pham
  • , S. Nowicki

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

PROBLEM: We evaluated the hypothesis that different tissue substructures in uteri may express decay accelerating factor (DAF), a complement regulatory protein that also may serve as ligand for bacterial attachment. METHOD: Purified Dr pili, anti-Dr pili IgG, anti-DAF (SCR-3) IgG, and fluorescein-isothiocyanate-conjugated secondary IgG were used for binding and inhibition experiments. RESULT: We observed staining of endometrial glands, spiral arterioles, and myometrial arteries with Dr adhesin (pili) and anti-DAF (SCR-3) IgG, and found variation in distribution and amount of Dr ligands in different individuals. Anti-DAF (SCR-3) IgG blocked the binding of Dr pili to the endometrium. CONCLUSION: Presence of DAF in endometrium may protect tissues from complement-induced damage. Differences between individuals in DAF density in the endometrium may affect sensitivity to attachment of Dr-bearing E. coli and/or complement activation.

Original languageEnglish
Pages (from-to)194-199
Number of pages6
JournalAmerican Journal of Reproductive Immunology
Volume32
Issue number3
StatePublished - 1994

Keywords

  • Colonization
  • DAF
  • Dr fimbriae
  • Dr ligands
  • E. coli
  • Urogenital tract

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