Zebrafish pigment cells develop directly from persistent highly multipotent progenitors

Neural crest cells are highly multipotent stem cells, but it remains unclear how their fate restriction to specific fates occurs. The direct fate restriction model hypothesises that migrating cells maintain full multipotency, whilst progressive fate restriction envisages fully multipotent cells tran...

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Main Authors: Subkhankulova, Tatiana, Sosa, Karen Camargo, Uroshlev, Leonid A., Nikaido, Masataka, Shriever, Noah, Kasianov, Artem S., Yang, Xueyan, Rodrigues, Frederico S. L. M., Carney, Tom J., Bavister, Gemma, Schwetlick, Hartmut, Dawes, Jonathan H. P., Rocco, Andrea, Makeev, Vsevolod J., Kelsh, Robert N.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/169754
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spelling sg-ntu-dr.10356-1697542023-08-06T15:38:17Z Zebrafish pigment cells develop directly from persistent highly multipotent progenitors Subkhankulova, Tatiana Sosa, Karen Camargo Uroshlev, Leonid A. Nikaido, Masataka Shriever, Noah Kasianov, Artem S. Yang, Xueyan Rodrigues, Frederico S. L. M. Carney, Tom J. Bavister, Gemma Schwetlick, Hartmut Dawes, Jonathan H. P. Rocco, Andrea Makeev, Vsevolod J. Kelsh, Robert N. Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Leukocyte Tyrosine Kinase Multipotent Stem Cell Neural crest cells are highly multipotent stem cells, but it remains unclear how their fate restriction to specific fates occurs. The direct fate restriction model hypothesises that migrating cells maintain full multipotency, whilst progressive fate restriction envisages fully multipotent cells transitioning to partially-restricted intermediates before committing to individual fates. Using zebrafish pigment cell development as a model, we show applying NanoString hybridization single cell transcriptional profiling and RNAscope in situ hybridization that neural crest cells retain broad multipotency throughout migration and even in post-migratory cells in vivo, with no evidence for partially-restricted intermediates. We find that leukocyte tyrosine kinase early expression marks a multipotent stage, with signalling driving iridophore differentiation through repression of fate-specific transcription factors for other fates. We reconcile the direct and progressive fate restriction models by proposing that pigment cell development occurs directly, but dynamically, from a highly multipotent state, consistent with our recently-proposed Cyclical Fate Restriction model. Published version This work was supported by Uehara Memorial Foundation (MN), Wellcome Trust VIP awards (M.N.), and BBSRC grants BB/ L00769X/1(R.N.K., H.S., T.S.) and BB/S015906/1 (R.N.K., J.H.P.D., K.C.S., G.B.) and BB/ L007789/1 and BB/S01604X/1 (A.R.), National Natural Science Foundation of China, Grant Number: 31000542 (X.Y.), Royal Society International Exchange Cost Share 2017 Russia award (R.N.K.), Russian Foundation of Basic Researcher grant 17-54-10014 (V.J.M.), Ministry of Science and Higher Education of the Russian Federation Grant number 075-15-2021-601 (V.J.M.), and University of Bath PhD Studentship and ORS award (T.J.C.). 2023-08-02T01:30:32Z 2023-08-02T01:30:32Z 2023 Journal Article Subkhankulova, T., Sosa, K. C., Uroshlev, L. A., Nikaido, M., Shriever, N., Kasianov, A. S., Yang, X., Rodrigues, F. S. L. M., Carney, T. J., Bavister, G., Schwetlick, H., Dawes, J. H. P., Rocco, A., Makeev, V. J. & Kelsh, R. N. (2023). Zebrafish pigment cells develop directly from persistent highly multipotent progenitors. Nature Communications, 14(1), 1258-. https://dx.doi.org/10.1038/s41467-023-36876-4 2041-1723 https://hdl.handle.net/10356/169754 10.1038/s41467-023-36876-4 36878908 2-s2.0-85149958709 1 14 1258 en Nature Communications © The Author(s) 2023. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Leukocyte Tyrosine Kinase
Multipotent Stem Cell
spellingShingle Science::Medicine
Leukocyte Tyrosine Kinase
Multipotent Stem Cell
Subkhankulova, Tatiana
Sosa, Karen Camargo
Uroshlev, Leonid A.
Nikaido, Masataka
Shriever, Noah
Kasianov, Artem S.
Yang, Xueyan
Rodrigues, Frederico S. L. M.
Carney, Tom J.
Bavister, Gemma
Schwetlick, Hartmut
Dawes, Jonathan H. P.
Rocco, Andrea
Makeev, Vsevolod J.
Kelsh, Robert N.
Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
description Neural crest cells are highly multipotent stem cells, but it remains unclear how their fate restriction to specific fates occurs. The direct fate restriction model hypothesises that migrating cells maintain full multipotency, whilst progressive fate restriction envisages fully multipotent cells transitioning to partially-restricted intermediates before committing to individual fates. Using zebrafish pigment cell development as a model, we show applying NanoString hybridization single cell transcriptional profiling and RNAscope in situ hybridization that neural crest cells retain broad multipotency throughout migration and even in post-migratory cells in vivo, with no evidence for partially-restricted intermediates. We find that leukocyte tyrosine kinase early expression marks a multipotent stage, with signalling driving iridophore differentiation through repression of fate-specific transcription factors for other fates. We reconcile the direct and progressive fate restriction models by proposing that pigment cell development occurs directly, but dynamically, from a highly multipotent state, consistent with our recently-proposed Cyclical Fate Restriction model.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Subkhankulova, Tatiana
Sosa, Karen Camargo
Uroshlev, Leonid A.
Nikaido, Masataka
Shriever, Noah
Kasianov, Artem S.
Yang, Xueyan
Rodrigues, Frederico S. L. M.
Carney, Tom J.
Bavister, Gemma
Schwetlick, Hartmut
Dawes, Jonathan H. P.
Rocco, Andrea
Makeev, Vsevolod J.
Kelsh, Robert N.
format Article
author Subkhankulova, Tatiana
Sosa, Karen Camargo
Uroshlev, Leonid A.
Nikaido, Masataka
Shriever, Noah
Kasianov, Artem S.
Yang, Xueyan
Rodrigues, Frederico S. L. M.
Carney, Tom J.
Bavister, Gemma
Schwetlick, Hartmut
Dawes, Jonathan H. P.
Rocco, Andrea
Makeev, Vsevolod J.
Kelsh, Robert N.
author_sort Subkhankulova, Tatiana
title Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
title_short Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
title_full Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
title_fullStr Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
title_full_unstemmed Zebrafish pigment cells develop directly from persistent highly multipotent progenitors
title_sort zebrafish pigment cells develop directly from persistent highly multipotent progenitors
publishDate 2023
url https://hdl.handle.net/10356/169754
_version_ 1779156486950223872