Journal Article

Experimental necrotizing enterocolitis induces neuroinflammation in the neonatal brain

Seo, Shogo, Catania, Vincenzo D., Guadagno, Jennifer, Li, Bo, Zani-Ruttenstock, Elke, Pierro, Agostino, Biouss, George, O’Connell, Joshua S., Svergun, Nataliia, Rahman, Abidur, Zani, Augusto, Antounians, Lina

2019

Overview

Background Necrotizing enterocolitis (NEC) is an inflammatory gastrointestinal disease primarily affecting preterm neonates. Neonates with NEC suffer from a degree of neurodevelopmental delay that is not explained by prematurity alone. There is a need to understand the pathogenesis of neurodevelopmental delay in NEC. In this study, we assessed the macroscopic and microscopic changes that occur to brain cell populations in specific brain regions in a neonatal mouse model of NEC. Moreover, we investigated the role of intestinal inflammation as part of the mechanism responsible for the changes observed in the brain of pups with NEC. Methods Brains of mice were assessed for gross morphology and cerebral cortex thickness (using histology). Markers for mature neurons, oligodendrocytes, neural progenitor cells, microglia, and astrocytes were used to quantify their cell populations in different regions of the brain. Levels of cell apoptosis in the brain were measured by Western blotting and immunohistochemistry. Endoplasmic reticulum (ER) stress markers and levels of pro-inflammatory cytokines (in the ileum and brain) were measured by RT-qPCR and Western blotting. A Pearson test was used to correlate the levels of cytokines (ELISA) in the brain and ileum and to correlate activated microglia and astrocyte populations to the severity of NEC. Results NEC pups had smaller brain weights, higher brain-to-body weight ratios, and thinner cortices compared to control pups. NEC pups had increased levels of apoptosis and ER stress. In addition, NEC was associated with a reduction in the number of neurons, oligodendrocytes, and neural progenitors in specific regions of the brain. Levels of pro-inflammatory cytokines and the density of activated microglia and astrocytes were increased in the brain and positively correlated with the increase in the levels pro-inflammatory cytokines in the gut and the severity of NEC damage respectively. Conclusions NEC is associated with severe changes in brain morphology, a pro-inflammatory response in the brain that alters cell homeostasis and density of brain cell populations in specific cerebral regions. We show that the severity of neuroinflammation is associated with the severity of NEC. Our findings suggest that early intervention during NEC may reduce the chance of acute neuroinflammation and cerebral damage.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Animals / Animals, Newborn / Apoptosis / Astrocytes / Biomedical and Life Sciences / Biomedicine / Birth weight / Body weight / Brain - metabolism / Brain - pathology / Brain diseases / Brain research / Care and treatment / Cerebral cortex / Complications and side effects / Cytology / Endoplasmic reticulum / Enterocolitis, Necrotizing - metabolism / Enterocolitis, Necrotizing - pathology / Enzyme-linked immunosorbent assay / Gastrointestinal diseases / Gene expression / Health aspects / Histology / Homeostasis / Hypoxia / Ileum / Immunohistochemistry / Immunology / Inflammation - metabolism / Inflammation - pathology / Inflammation Mediators - metabolism / Intestine / Ischemia / Laboratories / Mice / Mice, Inbred C57BL / Microbiota / Microglia / Necrosis / Necrotizing enterocolitis / Neonates / Neural progenitors / Neural stem cells / Neurobiology / Neuroinflammation / Neurology / Neurons / Neurosciences / Newborn babies / Newborn infants / NMR / Nuclear magnetic resonance / Oligodendrocytes / Progenitor cells / Risk factors / Traumatic brain injury / Western blotting