Mapping the Pairwise Choices Leading from Pluripotency to Human Bone, Heart, and Other Mesoderm Cell Types

Cell. 2016 Jul 14;166(2):451-467. doi: 10.1016/j.cell.2016.06.011.

Abstract

Stem-cell differentiation to desired lineages requires navigating alternating developmental paths that often lead to unwanted cell types. Hence, comprehensive developmental roadmaps are crucial to channel stem-cell differentiation toward desired fates. To this end, here, we map bifurcating lineage choices leading from pluripotency to 12 human mesodermal lineages, including bone, muscle, and heart. We defined the extrinsic signals controlling each binary lineage decision, enabling us to logically block differentiation toward unwanted fates and rapidly steer pluripotent stem cells toward 80%-99% pure human mesodermal lineages at most branchpoints. This strategy enabled the generation of human bone and heart progenitors that could engraft in respective in vivo models. Mapping stepwise chromatin and single-cell gene expression changes in mesoderm development uncovered somite segmentation, a previously unobservable human embryonic event transiently marked by HOPX expression. Collectively, this roadmap enables navigation of mesodermal development to produce transplantable human tissue progenitors and uncover developmental processes. VIDEO ABSTRACT.

Publication types

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

MeSH terms

  • Bone Morphogenetic Proteins / metabolism
  • Bone and Bones / cytology
  • Bone and Bones / metabolism
  • Heart / growth & development
  • Homeodomain Proteins / metabolism
  • Humans
  • Mesoderm / cytology*
  • Mesoderm / metabolism
  • Myocytes, Cardiac / metabolism
  • Pluripotent Stem Cells / metabolism
  • Primitive Streak / cytology
  • Primitive Streak / metabolism
  • Signal Transduction*
  • Single-Cell Analysis
  • Somites / metabolism
  • Stem Cells
  • Tumor Suppressor Proteins / metabolism
  • Wnt Proteins / antagonists & inhibitors
  • Wnt Proteins / metabolism

Substances

  • Bone Morphogenetic Proteins
  • HOPX protein, human
  • Homeodomain Proteins
  • Tumor Suppressor Proteins
  • Wnt Proteins