Endoderm

Mesoderm

Transcription factor

Biology

Gene

Induced pluripotent stem cell

Embryonic stem cell

Gastrulation

Wnt signaling pathway

Germ layer

Cell fate determination

Embryo

Stem cell

Signal transduction

Epiblast

Embryogenesis

Cell biology

Genetics

eLife

During gastrulation epiblast cells exit pluripotency as they specify and spatially arrange the three germ layers of the embryo. Similarly, human pluripotent stem cells (PSCs) undergo spatially organized fate specification on micropatterned surfaces. Since in vivo validation is not possible for the human, we developed a mouse PSC micropattern system and, with direct comparisons to mouse embryos, reveal the robust specification of distinct regional identities. BMP, WNT, ACTIVIN and FGF directed mouse epiblast-like cells to undergo an epithelial-to-mesenchymal transition and radially pattern posterior mesoderm fates. Conversely, WNT, ACTIVIN and FGF patterned anterior identities, including definitive endoderm. By contrast, epiblast stem cells, a developmentally advanced state, only specified anterior identities, but without patterning. The mouse micropattern system offers a robust scalable method to generate regionalized cell types present in vivo, resolve how signals promote distinct identities and generate patterns, and compare mechanisms operating in vivo and in vitro and across species.

Micropattern differentiation of mouse pluripotent stem cells recapitulates embryo regionalized cell fate patterning