Nature Communications (Jul 2024)

Engineering programmable material-to-cell pathways via synthetic notch receptors to spatially control differentiation in multicellular constructs

  • Mher Garibyan,
  • Tyler Hoffman,
  • Thijs Makaske,
  • Stephanie K. Do,
  • Yifan Wu,
  • Brian A. Williams,
  • Alexander R. March,
  • Nathan Cho,
  • Nicolas Pedroncelli,
  • Ricardo Espinosa Lima,
  • Jennifer Soto,
  • Brooke Jackson,
  • Jeffrey W. Santoso,
  • Ali Khademhosseini,
  • Matt Thomson,
  • Song Li,
  • Megan L. McCain,
  • Leonardo Morsut

DOI
https://doi.org/10.1038/s41467-024-50126-1
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 21

Abstract

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Abstract Synthetic Notch (synNotch) receptors are genetically encoded, modular synthetic receptors that enable mammalian cells to detect environmental signals and respond by activating user-prescribed transcriptional programs. Although some materials have been modified to present synNotch ligands with coarse spatial control, applications in tissue engineering generally require extracellular matrix (ECM)-derived scaffolds and/or finer spatial positioning of multiple ligands. Thus, we develop here a suite of materials that activate synNotch receptors for generalizable engineering of material-to-cell signaling. We genetically and chemically fuse functional synNotch ligands to ECM proteins and ECM-derived materials. We also generate tissues with microscale precision over four distinct reporter phenotypes by culturing cells with two orthogonal synNotch programs on surfaces microcontact-printed with two synNotch ligands. Finally, we showcase applications in tissue engineering by co-transdifferentiating fibroblasts into skeletal muscle or endothelial cell precursors in user-defined micropatterns. These technologies provide avenues for spatially controlling cellular phenotypes in mammalian tissues.