학술논문

Engineered human pluripotent-stem-cell-derived intestinal tissues with a functional enteric nervous system
Document Type
article
Source
Nature Medicine. 23(1)
Subject
Neurosciences
Stem Cell Research - Induced Pluripotent Stem Cell
Stem Cell Research - Nonembryonic - Human
Regenerative Medicine
Stem Cell Research - Induced Pluripotent Stem Cell - Human
Stem Cell Research - Embryonic - Human
Digestive Diseases
Congenital Structural Anomalies
Stem Cell Research
Pediatric
1.1 Normal biological development and functioning
5.2 Cellular and gene therapies
Development of treatments and therapeutic interventions
Underpinning research
Generic health relevance
Animals
Calcium
Cell Line
Chick Embryo
Enteric Nervous System
Gastrointestinal Motility
Hirschsprung Disease
Homeodomain Proteins
Humans
Immunohistochemistry
In Vitro Techniques
Induced Pluripotent Stem Cells
Interstitial Cells of Cajal
Intestines
Mice
Mice
SCID
Microscopy
Confocal
Models
Biological
Mutation
Myenteric Plexus
Neural Crest
Neurogenesis
Neuroglia
Neurons
Organoids
Permeability
Real-Time Polymerase Chain Reaction
Submucous Plexus
Tissue Engineering
Transcription Factors
Medical and Health Sciences
Immunology
Language
Abstract
The enteric nervous system (ENS) of the gastrointestinal tract controls many diverse functions, including motility and epithelial permeability. Perturbations in ENS development or function are common, yet there is no human model for studying ENS-intestinal biology and disease. We used a tissue-engineering approach with embryonic and induced pluripotent stem cells (PSCs) to generate human intestinal tissue containing a functional ENS. We recapitulated normal intestinal ENS development by combining human-PSC-derived neural crest cells (NCCs) and developing human intestinal organoids (HIOs). NCCs recombined with HIOs in vitro migrated into the mesenchyme, differentiated into neurons and glial cells and showed neuronal activity, as measured by rhythmic waves of calcium transients. ENS-containing HIOs grown in vivo formed neuroglial structures similar to a myenteric and submucosal plexus, had functional interstitial cells of Cajal and had an electromechanical coupling that regulated waves of propagating contraction. Finally, we used this system to investigate the cellular and molecular basis for Hirschsprung's disease caused by a mutation in the gene PHOX2B. This is, to the best of our knowledge, the first demonstration of human-PSC-derived intestinal tissue with a functional ENS and how this system can be used to study motility disorders of the human gastrointestinal tract.