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DOI 10.1038/pr.2015.261

Медицинская библиотека · Pediatric research · 2015

The viral dsRNA analogue poly (I:C) induces necrotizing enterocolitis in neonatal mice.

Ginzel Marco, Yu Yi, Klemann Christian, Feng Xiaoyan, von Wasielewski Reinhard, Park Joon-Keun, Hornef Mathias W, Torow Natalia, Vieten Gertrud, Ure Benno M, Kuebler Joachim F, Lacher Martin

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Necrotizing enterocolitis (NEC) is a life-threatening gastrointestinal disease in premature infants with high mortality and morbidity with uncertain pathogenesis. Recent research focused on the role of intraluminal bacteria and lipopolysaccharide (LPS). However, an additional role of viral agents in the pathogenesis of NEC has recently been postulated. We assessed the role of polyinosinic:polycytidylic acid (pIC) mimicking viral dsRNA in contributing to the development of NEC in neonatal mice.

METHODS

Four-d-old C57BL/6J pups were stressed by asphyxia and hypothermia twice daily. Animals were either fed by formula only (FO), formula containing LPS or pIC. After 72 h, mice were euthanized, intestines harvested, and the severity of NEC was assessed.

RESULTS

Breastfed mice showed no evidence of NEC. Very mild NEC-like lesions were observed in mice fed by FO. Supplementation of LPS or pIC to the formula led to increased intestinal tissue damage and inflammation compared with FO in a similar manner.

CONCLUSION

Our study demonstrates the ability of viral factors to induce NEC in neonatal mice even in the absence of LPS. Furthermore, we present a new mouse model of pIC-induced NEC which may be used to obtain further mechanistic insights in the pathogenesis of this disease.

Для цитирования: Ginzel Marco, Yu Yi, Klemann Christian, Feng Xiaoyan, von Wasielewski Reinhard, Park Joon-Keun, Hornef Mathias W, Torow Natalia, Vieten Gertrud, Ure Benno M, Kuebler Joachim F, Lacher Martin. The viral dsRNA analogue poly (I:C) induces necrotizing enterocolitis in neonatal mice.. Pediatric research. 2015. DOI: 10.1038/pr.2015.261.

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