Transcription and Signaling Regulators in Developing Neuronal Subtypes of Mouse and Human Enteric Nervous System.
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IF: 33.883
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Cited by: 67
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Abstract

The enteric nervous system (ENS) regulates gastrointestinal function via different subtypes of neurons, organized into fine-tuned neural circuits. It is not clear how cell diversity is created within the embryonic ENS; information required for development of cell-based therapies and models of enteric neuropathies. We aimed to identify proteins that regulate ENS differentiation and network formation. We generated and compared RNA expression profiles of the entire ENS, ENS progenitor cells, and non-ENS gut cells of mice, collected at embryonic days 11.5 and 15.5, when different subtypes of neurons are formed. Gastrointestinal tissues from R26ReYFP reporter mice crossed to Sox10-CreERT2 or Wnt1-Cre mice were dissected and the 6 populations of cells were isolated by flow cytometry. We used histochemistry to map differentially expressed proteins in mouse and human gut tissues at different stages of development, in different regions. We examined enteric neuronal diversity and gastric function in Wnt1-Cre x Sox6fl/fl mice, which do not express the Sox6 gene in the ENS. We identified 147 transcription and signaling factors that varied in spatial and temporal expression during development of the mouse ENS. Of the factors also analyzed in human ENS, most were conserved. We uncovered 16 signaling pathways (such as fibroblast growth factor and Eph/ephrin pathways). Transcription factors were grouped according to their specific expression in enteric progenitor cells (such as MEF2C), enteric neurons (such as SOX4), or neuron subpopulations (such as SATB1 and SOX6). Lack of SOX6 in the ENS reduced the numbers of gastric dopamine neurons and delayed gastric emptying. Using transcriptome and histochemical analyses of the developing mouse and human ENS, we mapped expression patterns of transcription and signaling factors. Further studies of these candidate determinants might elucidate the mechanisms by which enteric stem cells differentiate into neuronal subtypes and form distinct connectivity patterns during ENS development. We found expression of SOX6 to be required for development of gastric dopamine neurons.

Keywords

Gastric Motility
HOX
Neural Crest
Tyrosine Hydroxylase

MeSH terms

Animals
Autocrine Communication
Dopaminergic Neurons
Enteric Nervous System
Gastric Emptying
Gene Expression Profiling
Gene Expression Regulation, Developmental
Genotype
Gestational Age
Humans
Mice, Knockout
Paracrine Communication
Phenotype
SOXD Transcription Factors
SOXE Transcription Factors
Signal Transduction
Species Specificity
Stomach
Transcription Factors
Transcription, Genetic

Authors

Memic, Fatima
Knoflach, Viktoria
Morarach, Khomgrit
Sadler, Rebecca
Laranjeira, Catia
Hjerling-Leffler, Jens
Sundström, Erik
Pachnis, Vassilis
Marklund, Ulrika

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