The goals of the proposed research are to determine the mechanisms that lead to the development of necrotizing enterocolitis (NEC), and to determine novel therapeutic strategies for this devastating disease. To do so, we will explore novel roles of the Aryl Hydrocarbon Receptor (AHR) in the pathogenesis of NEC through its previously unrecognized effects in reducing the inflammatory response to colonizing bacteria in the premature intestine. We have discovered that toll like receptor 4 (TLR4) activation on the intestinal epithelium plays a critical role in NEC development, as mice lacking TLR4 on the intestinal epithelium are protected from NEC. We also determined that TLR4 expression on the intestinal epithelium is higher in the premature human and mouse intestine, which in mice reflects a novel role played by TLR4 in the regulation of intestinal differentiation. Importantly, the factors responsible for the elevated TLR4 signaling, and mechanisms capable of restraining TLR4 in the premature intestine, remain largely unknown. We now show that AHR expression is low in mouse and human NEC where TLR4 is high, and that activation of AHR within the newborn intestinal mucosa by dietary ligands, including those present in breast milk, restrain TLR4 signaling and attenuate NEC. Further, the administration of AHR ligands to the pregnant mother prevents NEC in the offspring. Importantly, we have identified novel AHR ligands that can prevent NEC in mice through reduced TLR4 signaling, and which reduce inflammation in human NEC tissue ex vivo. We thus hypothesize that AHR in the newborn gut plays a previously unrecognized role in restraining the hyper-inflammatory response of the newborn intestinal mucosa to colonizing microbes by limiting TLR4 signaling in the intestinal epithelium, thus protecting against NEC, and further, that activation of AHR by dietary factors including those in breast milk, can restrain TLR4 signaling and prevent NEC. Further, we hypothesize that the administration of an AHR ligand to the pregnant mother can reduce NEC severity in the pup. Finally, we propose that a recently discovered AHR ligand in our lab, termed ?A18?, may represent a novel strategy for NEC prevention and treatment. We will test this hypothesis in 3 aims:
Aim 1 : To understand the role of the Aryl Hydrocarbon Receptor in the newborn intestinal epithelium in the pathogenesis and treatment of NEC;
Aim 2 To determine the effects and mechanisms by which the administration of a diet rich in AHR ligands to the pregnant mother protects against NEC in the offspring.
Aim 3. To evaluate the role of a recently discovered AHR agonist, A18, in the prevention and treatment of experimental NEC in mice and piglets. These studies will make a significant conceptual advance by defining how dietary ligands can activate AHR and reduce inflammation in the premature intestinal epithelium, and provide a novel approach for NEC prevention through intra-partum administration of novel AHR ligands.

Public Health Relevance

. Necrotizing enterocolitis (NEC) is the leading cause of death from gastrointestinal disease in premature infants, and for which there exists no effective cure, and in which a third of patients will develop significant lung injury. The current proposal seeks to understand the causes of NEC by focusing on how activation of the immune system can lead to the development of this disease, and to identify novel agents which when added to the diet can prevent NEC in premature infants. We have also identified a strategy whereby dietary factors can be given to the pregnant mother in order to prevent the development of NEC in her offspring.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK117186-02
Application #
9670781
Study Section
Gastrointestinal Mucosal Pathobiology Study Section (GMPB)
Program Officer
Hamilton, Frank A
Project Start
2018-04-01
Project End
2022-02-28
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Surgery
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
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