A model of the embryonic human trunk attains a more mature developmental stage than previous models.
Research on the developmental processes that form the mammalian trunk — the part of the body spanning from head to limbs — has entered a new chapter in recent years with the establishment of tractable in vitro models. Starting from pluripotent stem cells, these models reconstruct early embryonic events in vitro to generate structures that resemble the somites and the neural tube in morphology and in cell lineage patterning1,2,3,4,5,6,7. Writing in Nature Biotechnology, Gribaudo et al. have now taken the field one step further8. They describe the generation of human organoids that recapitulate spatial and temporal patterning of the spinal cord up to a much later stage than in previously reported systems. Importantly, their model not only gives rise to terminally differentiated cell types but also exhibits accurate regionalization of the trunk spinal cord. Their experiments demonstrate that it should be possible to push these systems to study even later aspects of development, such as HOX gene–dependent regionalization.
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Fig. 1: A stem cell-derived model of human trunk development recapitulates spinal cord differentiation and patterning.
References
Sanaki-Matsumiya, M. et al. Nat. Commun. 13, 2325 (2022).
Miao, Y. et al. Nature https://doi.org/10.1038/s41586-022-05655-4 (2022).
Article
PubMed
PubMed Central
Google Scholar
Yamanaka, Y. et al. Nature https://doi.org/10.1038/s41586-022-05649-2 (2022).
Article
PubMed
Google Scholar
Anand, G. M. et al. Cell 186, 497–512.e23 (2023).
Article
CAS
PubMed
Google Scholar
Yaman, Y. I. & Ramanathan, S. Cell 186, 513–527.e19 (2023).
Article
CAS
PubMed
Google Scholar
van den Brink, S. C. et al. Nature 582, 405–409, https://doi.org/10.1038/s41586-020-2024-3 (2020).
Article
CAS
PubMed
Google Scholar
Veenvliet, J. V. et al. Science 370, eaba4937 (2020).
Gribaudo, S. et al. Nat. Biotechnol. https://doi.org/10.1038/s41587-023-01956-9 (2023).
Article
PubMed
Google Scholar
Bénazéraf, B. & Pourquié, O. Annu. Rev. Cell Dev. Biol. 29, 1–26 (2013).
Article
PubMed
Google Scholar
Binagui-Casas, A., Dias, A., Guillot, C., Metzis, V. & Saunders, D. Curr. Opin. Cell Biol. 73, 133–140 (2021).
Article
CAS
PubMed
Google Scholar
Duboule, D. Dev. Biol. 484, 75–87 (2022).
Article
CAS
PubMed
Google Scholar
Philippidou, P. & Dasen, J. S. Neuron 80, 12–34 (2013).
Article
CAS
PubMed
Google Scholar
Beccari, L. et al. Nature 562, 272–276 (2018).
Article
CAS
PubMed
Google Scholar
Download references
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Authors and Affiliations
Department of Genetics, Harvard Medical School, Boston, MA, USA
Yuchuan Miao & Olivier Pourquié
Department of Pathology, Brigham and Women’s Hospital, Boston, MA, USA
Yuchuan Miao & Olivier Pourquié
Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA
Olivier Pourquié
Corresponding author
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The authors declare no competing interests.
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Miao, Y., Pourquié, O. Modeling human trunk development.
Nat Biotechnol (2023). https://doi.org/10.1038/s41587-023-02048-4
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Published: 16 November 2023
DOI: https://doi.org/10.1038/s41587-023-02048-4
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