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Biology subjects

Smirnova, N. P.

Publications and source records attributed to Smirnova, N. P..

2 recordsLinked to original sources

Co-aggregation of pre-conditioned cell populations drives controlled lineage bias and formation of gut tube-like structures in human stem cell-based embryo models

Human stem cell-based embryo models (hSCBEMs) provide a powerful platform for investigating post-implantation human embryo development but are frequently hindered by variability in growth and morphogenesis as well as incomplete lineage representations. Here, we present a modular hSCBEM aggregation approach based on co-aggregation of differentially pre-conditioned, human pluripotent stem cell derived cells pools. Using this strategy, we generated hSCBEM with consistent morphotypes that targets robust morphogenesis of gut tube-like structures in combination with mesodermal lineages. Our findings demonstrate that co-aggregating defined cellular heterogeneity represents a versatile approach to specifically guide self-organization in hSCBEMs while improving reproducibility and developmental fidelity. The approach provides a robust platform for supervised morphogenesis in hSCBEMs.

developmental biology↗

Reconstituting epiblast-extraembryonic endoderm interactions restores anterior-ventral patterning in stem cell-based embryo models.

During mammalian embryogenesis, reciprocal interactions between the epiblast and extraembryonic endoderm are critical for germ layer specification and body plan development during gastrulation. Gastruloids recapitulate aspects of gastrulation in the absence of extraembryonic cues, resulting in a predominantly posteriorized and dorsalized phenotype with a limited lineage diversity. Here, we establish a modular co-aggregation ("aggregoid") strategy that spatially couples embryonic and extraembryonic endoderm-like cells to reconstruct key interactions in vitro. This drives self-organized anterior-ventral patterning together with the emergence of node- and notochord-like structures, enriched endodermal populations, and increased mesodermal diversity, including cardiopharyngeal lineages and vascular endothelium. Our findings demonstrate that modular engineering of lineage interactions can direct self-organized patterning in stem-cell-based embryo models and provide a versatile framework for generating defined morphotypes.

developmental biology↗