Deterministic HOX patterning in human pluripotent stem cell-derived neuroectoderm.

Lippmann ES, Williams CE, Ruhl DA, Estevez-Silva MC, Chapman ER, Coon JJ, Ashton RS
Stem Cell Reports. 2015 4 (4): 632-44

PMID: 25843047 · PMCID: PMC4400649 · DOI:10.1016/j.stemcr.2015.02.018

Colinear HOX expression during hindbrain and spinal cord development diversifies and assigns regional neural phenotypes to discrete rhombomeric and vertebral domains. Despite the precision of HOX patterning in vivo, in vitro approaches for differentiating human pluripotent stem cells (hPSCs) to posterior neural fates coarsely pattern HOX expression thereby generating cultures broadly specified to hindbrain or spinal cord regions. Here, we demonstrate that successive activation of fibroblast growth factor, Wnt/β-catenin, and growth differentiation factor signaling during hPSC differentiation generates stable, homogenous SOX2(+)/Brachyury(+) neuromesoderm that exhibits progressive, full colinear HOX activation over 7 days. Switching to retinoic acid treatment at any point during this process halts colinear HOX activation and transitions the neuromesoderm into SOX2(+)/PAX6(+) neuroectoderm with predictable, discrete HOX gene/protein profiles that can be further differentiated into region-specific cells, e.g., motor neurons. This fully defined approach significantly expands capabilities to derive regional neural phenotypes from diverse hindbrain and spinal cord domains.

Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.

MeSH Terms (14)

beta Catenin Fibroblast Growth Factors Gene Expression Regulation, Developmental Homeodomain Proteins Humans Neural Plate Organ Specificity Pluripotent Stem Cells Signal Transduction Stem Cells Transcriptional Activation Transcriptome Tretinoin Wnt Proteins

Connections (1)

This publication is referenced by other Labnodes entities: