Catalpol promotes the generation of cerebral organoids with oRGs through activation of STAT3 signalingopen access
- Authors
- Lee, Yoo-Jung; Cho, Byounggook; Kwon, Daeyeol; Kim, Yunkyung; An, Saemin; Kang, Soi; Kim, Jongpil
- Issue Date
- May-2025
- Publisher
- John Wiley and Sons Inc
- Keywords
- Catalpol; cerebral organoids; outer radial glia cells; STAT3 signaling
- Citation
- Bioengineering and Translational Medicine, v.10, no.3, pp 1 - 11
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- Bioengineering and Translational Medicine
- Volume
- 10
- Number
- 3
- Start Page
- 1
- End Page
- 11
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/56663
- DOI
- 10.1002/btm2.10746
- ISSN
- 2380-6761
2380-6761
- Abstract
- The generation of human cortical organoids containing outer radial glia (oRG) cells is crucial for modeling neocortical development. Here we show that Catalpol, an iridoid glucoside derived from Rehmannia glutinosa, significantly enhances the generation of cerebral organoids with expanded oRG populations and increased neurogenic potential. Catalpol-treated organoids exhibited thicker ventricular zone/subventricular zone (VZ/SVZ) and outer subventricular zone (oSVZ) regions, with increased numbers of SOX2 + HOPX+ and SOX2 + TNC+ oRG cells and elevated expression of oRG markers HOPX and FAM107A. We found that Catalpol promoted oRG generation through non-vertical divisions of ventricular radial glia (vRG) cells, indicating enhanced oRG generation via asymmetrical divisions. Furthermore, we demonstrated that Catalpol augmented oRG cell numbers through activation of the STAT3 signaling pathway. These findings highlight Catalpol's potential in promoting the generation of cerebral organoids with expanded oRG populations and increased neurogenic potential through STAT3 activation, offering new insights into neocortical development modeling. © 2024 The Author(s). Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.
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Collections - College of Natural Science > Department of Chemistry > 1. Journal Articles

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