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Review

Timing and Graded BMP Signalling Determines Fate of Neural Crest and Ectodermal Placode Derivatives from Pluripotent Stem Cells

1
LBN, Laboratory of Bioengineering and Nanoscience, University of Montpellier, 34193 Montpellier, France
2
Harvard Medical School, Massachusetts Eye and Ear Infirmary Boston, MA 02114, USA
*
Authors to whom correspondence should be addressed.
Biomedicines 2024, 12(10), 2262; https://doi.org/10.3390/biomedicines12102262
Submission received: 9 September 2024 / Revised: 29 September 2024 / Accepted: 1 October 2024 / Published: 4 October 2024
(This article belongs to the Special Issue Pluripotent Stem Cell: Current Understanding and Future Directions)

Abstract

Pluripotent stem cells (PSCs) offer many potential research and clinical benefits due to their ability to differentiate into nearly every cell type in the body. They are often used as model systems to study early stages of ontogenesis to better understand key developmental pathways, as well as for drug screening. However, in order to fully realise the potential of PSCs and their translational applications, a deeper understanding of developmental pathways, especially in humans, is required. Several signalling molecules play important roles during development and are required for proper differentiation of PSCs. The concentration and timing of signal activation are important, with perturbations resulting in improper development and/or pathology. Bone morphogenetic proteins (BMPs) are one such key group of signalling molecules involved in the specification and differentiation of various cell types and tissues in the human body, including those related to tooth and otic development. In this review, we describe the role of BMP signalling and its regulation, the consequences of BMP dysregulation in disease and differentiation, and how PSCs can be used to investigate the effects of BMP modulation during development, mainly focusing on otic development. Finally, we emphasise the unique role of BMP4 in otic specification and how refined understanding of controlling its regulation could lead to the generation of more robust and reproducible human PSC-derived otic organoids for research and translational applications.
Keywords: bone morphogenetic proteins; human pluripotent stem cells; human cell models; organoids; pre-placodal ectoderm; otic lineage bone morphogenetic proteins; human pluripotent stem cells; human cell models; organoids; pre-placodal ectoderm; otic lineage

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MDPI and ACS Style

Chung, K.; Millet, M.; Rouillon, L.; Zine, A. Timing and Graded BMP Signalling Determines Fate of Neural Crest and Ectodermal Placode Derivatives from Pluripotent Stem Cells. Biomedicines 2024, 12, 2262. https://doi.org/10.3390/biomedicines12102262

AMA Style

Chung K, Millet M, Rouillon L, Zine A. Timing and Graded BMP Signalling Determines Fate of Neural Crest and Ectodermal Placode Derivatives from Pluripotent Stem Cells. Biomedicines. 2024; 12(10):2262. https://doi.org/10.3390/biomedicines12102262

Chicago/Turabian Style

Chung, Keshi, Malvina Millet, Ludivine Rouillon, and Azel Zine. 2024. "Timing and Graded BMP Signalling Determines Fate of Neural Crest and Ectodermal Placode Derivatives from Pluripotent Stem Cells" Biomedicines 12, no. 10: 2262. https://doi.org/10.3390/biomedicines12102262

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