DNA microbeads for spatio-temporally controlled morphogen release within organoids

Organoids are transformative in vitro model systems that mimic features of the corresponding tissue in vivo. However, across tissue types and species, organoids still often fail to reach full maturity and function because biochemical cues cannot be provided from within the organoid to guide their development. Here we introduce nanoengineered DNA microbeads with tissue mimetic tunable stiffness for implementing spatio-temporally controlled morphogen gradients inside of organoids at any point in their development. Using medaka retinal organoids and early embryos, we show that DNA microbeads can be integrated into embryos and organoids by microinjection and erased in a non-invasive manner with light. Coupling a recombinant surrogate Wnt to the DNA microbeads, we demonstrate the spatio-temporally controlled morphogen release from the microinjection site, which leads to morphogen gradients resulting in the formation of retinal pigmented epithelium while maintaining neuroretinal cell types. Thus, we bioengineered retinal organoids to more closely mirror the cell type diversity of in vivo retinae. Owing to the facile, one-pot fabrication process, the DNA microbead technology can be adapted to other organoid systems for improved tissue mimicry.

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Publication Details

Journal
Nature Nanotechnology
Published
2024-09-09
DOI
https://doi.org/10.1038/s41565-024-01779-y
Citations
19
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
4.44

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article

DNA microbeads for spatio-temporally controlled morphogen release within organoids

Oliver M. Drozdowski, Christina Schlagheck, Cassian Afting, Joachim Wittbrodt et al.
19 citations
Nature Nanotechnology
Retinal Development and Disorders
4.44
article

DNA microbeads for spatio-temporally controlled morphogen release within organoids

Oliver M. Drozdowski, Christina Schlagheck, Cassian Afting, Joachim Wittbrodt, Kerstin Göpfrich, Ulrich S. Schwarz, Tobias Walther
article en
19 citations

Abstract

Organoids are transformative in vitro model systems that mimic features of the corresponding tissue in vivo. However, across tissue types and species, organoids still often fail to reach full maturity and function because biochemical cues cannot be provided from within the organoid to guide their development. Here we introduce nanoengineered DNA microbeads with tissue mimetic tunable stiffness for implementing spatio-temporally controlled morphogen gradients inside of organoids at any point in their development. Using medaka retinal organoids and early embryos, we show that DNA microbeads can be integrated into embryos and organoids by microinjection and erased in a non-invasive manner with light. Coupling a recombinant surrogate Wnt to the DNA microbeads, we demonstrate the spatio-temporally controlled morphogen release from the microinjection site, which leads to morphogen gradients resulting in the formation of retinal pigmented epithelium while maintaining neuroretinal cell types. Thus, we bioengineered retinal organoids to more closely mirror the cell type diversity of in vivo retinae. Owing to the facile, one-pot fabrication process, the DNA microbead technology can be adapted to other organoid systems for improved tissue mimicry.

Nature NanotechnologyVol. 19(12)
Heidelberg University (DE), Heidelberg University of Education (DE), Max Planck Institute for Medical Research (DE), Max Planck School Matter to Life, Heidelberg Institute for Theoretical Studies (DE), Heidelberg University (US)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Max-Planck-Gesellschaft, Studienstiftung des Deutschen Volkes
Life in Land
Openalex Percentile: Top 5%
Retinal Development and Disorders
4.44
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