P-selectin expression, neutrophil infiltration, and histologic injury in neonates with necrotizing enterocolitis

J Pediatr Surg. 2005 Jun;40(6):942-7; discussion 947-8. doi: 10.1016/j.jpedsurg.2005.03.027.

Abstract

Background/purpose: P-selectin promotes adherence of leukocytes to the endothelium in inflammatory processes. The aim of this study was to investigate the expression of P-selectin and its role in the development of inflammation in neonates with necrotizing enterocolitis (NEC).

Methods: Twenty-nine intestinal specimens from 13 neonates with NEC and 7 control neonates with congenital gastrointestinal abnormalities were studied. Histologic damage, immunohistochemical expression of P-selectin, and polymorphonuclear cell infiltrate were graded blindly. Mann-Whitney U and Spearman rank tests were used to compare grades.

Results: Expression of P-selectin was increased in NEC compared with controls in both medium-sized vessels (P = .03) and in the microcirculation (P = .03). P-selectin expression on medium-sized vessels correlated with the degree of histologic injury (P = .02, r = 0.425). P-selectin expression was greatest in areas of active inflammation but markedly lower in necrotic areas. The degree of polymorphonuclear cell infiltration strongly correlated with P-selectin expression on both medium-sized vessels (P = .004, r = 0.513) and the microcirculation (P = .001, r = 0.578).

Conclusions: Expression of P-selectin is increased in medium-sized vessels and in the microcirculation in intestinal specimens of neonates with NEC compared with neonatal controls. Expression of P-selectin is associated with the recruitment of polymorphonuclear cells and the severity of histologic injury, although P-selectin expression is lost in necrotic tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enterocolitis, Necrotizing / immunology
  • Enterocolitis, Necrotizing / metabolism*
  • Enterocolitis, Necrotizing / pathology
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Premature
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Intestinal Mucosa / blood supply
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / pathology*
  • Leukocyte Elastase / analysis
  • Microcirculation / metabolism
  • Neutrophil Infiltration*
  • P-Selectin / metabolism*
  • Platelet Membrane Glycoprotein IIb / analysis
  • Retrospective Studies
  • Statistics, Nonparametric

Substances

  • P-Selectin
  • Platelet Membrane Glycoprotein IIb
  • Leukocyte Elastase