Dithizone-induced Paneth cell disruption significantly decreases intestinal perfusion in the murine small intestine
Autor: | Jennifer N. Berger, Misty Good, Steven J. McElroy, Huyiu Gong |
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Rok vydání: | 2019 |
Předmět: |
Small
Pediatrics Intestinal microvasculature Mice chemistry.chemical_compound 0302 clinical medicine Necrotizing enterocolitis Ischemia Intestine Small Diphtheria Toxin Pediatric General Medicine Intestine medicine.anatomical_structure Dithizone 030220 oncology & carcinogenesis medicine.symptom Perfusion Biotechnology Signal Transduction Paneth Cells Nitric Oxide Article Nitric oxide Paediatrics and Reproductive Medicine 03 medical and health sciences Enterocolitis Necrotizing 030225 pediatrics medicine Animals Animal model Diphtheria toxin Enterocolitis Animal business.industry Microcirculation Perinatal Period - Conditions Originating in Perinatal Period medicine.disease Molecular biology Small intestine Disease Models Animal chemistry Disease Models Pediatrics Perinatology and Child Health Paneth cell Surgery Necrotizing Digestive Diseases business Vasoconstriction |
Zdroj: | J Pediatr Surg Journal of pediatric surgery, vol 54, iss 11 |
ISSN: | 0022-3468 |
DOI: | 10.1016/j.jpedsurg.2019.02.021 |
Popis: | PurposeNecrotizing enterocolitis is associated with decreased intestinal perfusion and ischemia. Paneth cells, specialized epithelial cells, have been shown to regulate the intestinal vasculature and disruption of these cells has been associated with NEC. We hypothesized that Paneth cell disruption in immature mice intestine would decrease the perfusion of the intestinal microvasculature.MethodsPaneth cells were disrupted in P14-16 mice using chemical (dithizone) and transgenic (diphtheria toxin) methodology. Six hours after Paneth cell disruption, Dylight 488 was injected directly into the left ventricle and allowed to perfuse for 5 minutes prior to intestinal harvesting. Tissue samples were evaluated with confocal fluorescence microscopy to quantify intestinal perfusion and samples were quantified by real time RT-PCR for gene expression.ResultsDithizone treatment significantly decreased intestinal perfusion compared to controls (p 0.21). Intestines from all treatment groups had similar PECAM staining, but intestines treated with dithizone had significantly decreased nNOS and iNOS gene expression compared to controls (p |
Databáze: | OpenAIRE |
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