Precision-based modeling approaches for necrotizing enterocolitis

Dis Model Mech. 2020 Jun 24;13(6):dmm044388. doi: 10.1242/dmm.044388.

Abstract

Necrotizing enterocolitis (NEC) is the leading cause of death from gastrointestinal disease in premature infants and remains stubbornly difficult to treat in many cases. Much of our understanding of NEC pathogenesis has been gained through the study of highly translational animal models. However, most models of NEC are limited by their overall complexity and by the fact that they do not incorporate human tissue. To address these limitations, investigators have recently developed precision-based ex vivo models of NEC, also termed 'NEC-in-a-dish' models, which provide the opportunity to increase our understanding of this disease and for drug discovery. These approaches involve exposing intestinal cells from either humans or animals with or without NEC to a combination of environmental and microbial factors associated with NEC pathogenesis. This Review highlights the current progress in the field of NEC model development, introduces NEC-in-a-dish models as a means to understand NEC pathogenesis and examines the fundamental questions that remain unanswered in NEC research. By answering these questions, and through a renewed focus on precision model development, the research community may finally achieve enduring success in improving the outcome of patients with this devastating disease.

Keywords: Enteroid; Necrotizing enterocolitis; Premature intestine; Toll-like receptor 4.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Cells, Cultured
  • Disease Models, Animal
  • Enterocolitis, Necrotizing* / metabolism
  • Enterocolitis, Necrotizing* / microbiology
  • Enterocolitis, Necrotizing* / pathology
  • Humans
  • Intestine, Small* / metabolism
  • Intestine, Small* / microbiology
  • Intestine, Small* / pathology
  • Organoids
  • Signal Transduction
  • Toll-Like Receptor 4 / metabolism

Substances

  • Toll-Like Receptor 4