Advanced ScienceDevelopmental BiologyPeer-reviewed journal article
Symmetry breaking of hPSCs in micropattern generates a polarized spinal cord-like organoid (pSCO) with dorsoventral organization
Kyubin Seo, Subin ChoiD, Hyogeun ShiniD, Aeri ShiniD, Ju‐Hyun LeeiD, June Hoan KimiD, Boram LeeiD, Hwanseok JangiD, Young‐Ju Kim, Hyo Min ChoiD, Yongdoo ParkiD, Hee Youn KimiD, Taeseob LeeiD, Woong‐Yang ParkiD, Yong Jun KimiD, Esther YangiD, Dongho GeumiD, Hyun KimiD, Il‐Joo ChoiD, Sang‐Hyuk LeeiD, Jae Ryun Ryu, Woong SuniD
Abstract
Brain organoid research is advancing, but generation of organoids with proper axis formation, which could lead to spatially ordered structures for complex brain structure and function, still remains a challenge. Axis formation and related spatial cell organization in the CNS are initiated by the symmetry breaking during the early embryo development. It has been demonstrated that the geometrically confined culture of human pluripotent stem cells (hPSCs) can be used to induce symmetry breaking and regionalized cell differentiation. In this study, we generated a polarized spinal cord organoid with a self-organized dorsoventral (DV) organization, using 2D cell patterning by geometric confinement. Initially, the application of caudalization signals to hPSCs promoted the regionalized cell differentiation along the radial axis and sprouting-like protrusion morphogenesis in cell colonies confined to ECM protein micropatterns. Detachment of colonies turned them into extended spinal cord-like organoids which maintained center- and edge-derived two poles. Further analyses including single cell RNA sequencing and spatial transcriptome analysis unveiled that these organoids contained rich repertoire of developing spinal cord cells and exhibited the spatially ordered DV domain formation along the long axis without external organizing signals. Modulation of BMP and Shh signaling can control the extent of DV coverage in organoids following the principles of embryo patterning. Our study provides a simple, and precisely controllable method to generate spatially-ordered organoids for understanding of biological principles of cell patterning and axis formation during neural development.
- organism: human
- assay: bulk RNA-seq
- assay: spatial transcriptomics
- research focus: cell type annotation
- research focus: differential expression
- approach: statistical model
- Citations
- 33
- FWCI
- 2.40
- Field percentile
- top 10%
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