Necrotizing enterocolitis in a mouse model leads to widespread renal inflammation, acute kidney injury, and disruption of renal tight junction proteins

Pediatr Res. 2015 Nov;78(5):527-32. doi: 10.1038/pr.2015.146. Epub 2015 Aug 13.

Abstract

Background: Necrotizing enterocolitis (NEC) is a devastating condition affecting premature infants and leads to high mortality and chronic morbidity. Severe form of NEC is associated with acute renal failure, fluid imbalance, hyponatremia, and acidosis. We investigated the effect of NEC on tight junction (TJ) proteins in kidneys using a NEC mouse model to investigate the basis for the observed renal dysfunction.

Methods: NEC was induced in C57BL/6 mice by formula feeding and subjecting them to periods of hypoxia and cold stress. NEC was confirmed by gross and histological examination. We studied various markers of inflammation in kidneys and investigated changes in expression of several TJ proteins and AQP2 using immunofluorecent staining and western blotting.

Results: We found markedly increased expression of NFκB, TGFβ, and ERK1/2 along with claudin-1, -2, -3, -4, -8, and AQP-2 in NEC kidneys. The membrane localization of claudin-2 was altered in the NEC kidneys and its immunostaining signal at TJ was disrupted.

Conclusion: NEC led to a severe inflammatory response not only in the gut but also in the kidneys. NEC increased expression of several TJ proteins and caused disruption of claudin-2 in renal tubules. These observed changes can help explain some of the clinical findings observed in NEC.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acute Kidney Injury / etiology*
  • Acute Kidney Injury / metabolism
  • Acute Kidney Injury / pathology
  • Animals
  • Aquaporin 2 / metabolism
  • Claudins / metabolism
  • Cold Temperature
  • Cold-Shock Response
  • Disease Models, Animal
  • Enterocolitis, Necrotizing / etiology*
  • Enterocolitis, Necrotizing / metabolism
  • Enterocolitis, Necrotizing / pathology
  • Humans
  • Hypoxia / complications
  • Infant Formula
  • Infant, Newborn
  • Inflammation Mediators / metabolism
  • Intestinal Mucosa / metabolism
  • Intestines / pathology
  • Kidney / metabolism*
  • Kidney / pathology
  • Mice, Inbred C57BL
  • Nephritis / etiology*
  • Nephritis / metabolism
  • Nephritis / pathology
  • Signal Transduction
  • Tight Junction Proteins / metabolism*
  • Tight Junctions / metabolism*
  • Tight Junctions / pathology

Substances

  • Aqp2 protein, mouse
  • Aquaporin 2
  • Claudins
  • Cldn2 protein, mouse
  • Inflammation Mediators
  • Tight Junction Proteins