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Multicolor strategies for investigating clonal expansion and tissue plasticity
Understanding the generation of complexity in living organisms requires the use of lineage tracing tools at a multicellular scale. In this review, we describe the different multicolor strategies focusing on mouse models expressing several fluorescent reporter proteins, generated by classical (MADM,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858928/ https://www.ncbi.nlm.nih.gov/pubmed/35187598 http://dx.doi.org/10.1007/s00018-021-04077-1 |
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author | Dumas, L. Clavreul, S. Michon, F. Loulier, K. |
author_facet | Dumas, L. Clavreul, S. Michon, F. Loulier, K. |
author_sort | Dumas, L. |
collection | PubMed |
description | Understanding the generation of complexity in living organisms requires the use of lineage tracing tools at a multicellular scale. In this review, we describe the different multicolor strategies focusing on mouse models expressing several fluorescent reporter proteins, generated by classical (MADM, Brainbow and its multiple derivatives) or acute (StarTrack, CLoNe, MAGIC Markers, iOn, viral vectors) transgenesis. After detailing the multi-reporter genetic strategies that serve as a basis for the establishment of these multicolor mouse models, we briefly mention other animal and cellular models (zebrafish, chicken, drosophila, iPSC) that also rely on these constructs. Then, we highlight practical applications of multicolor mouse models to better understand organogenesis at single progenitor scale (clonal analyses) in the brain and briefly in several other tissues (intestine, skin, vascular, hematopoietic and immune systems). In addition, we detail the critical contribution of multicolor fate mapping strategies in apprehending the fine cellular choreography underlying tissue morphogenesis in several models with a particular focus on brain cytoarchitecture in health and diseases. Finally, we present the latest technological advances in multichannel and in-depth imaging, and automated analyses that enable to better exploit the large amount of data generated from multicolored tissues. |
format | Online Article Text |
id | pubmed-8858928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-88589282022-02-23 Multicolor strategies for investigating clonal expansion and tissue plasticity Dumas, L. Clavreul, S. Michon, F. Loulier, K. Cell Mol Life Sci Review Understanding the generation of complexity in living organisms requires the use of lineage tracing tools at a multicellular scale. In this review, we describe the different multicolor strategies focusing on mouse models expressing several fluorescent reporter proteins, generated by classical (MADM, Brainbow and its multiple derivatives) or acute (StarTrack, CLoNe, MAGIC Markers, iOn, viral vectors) transgenesis. After detailing the multi-reporter genetic strategies that serve as a basis for the establishment of these multicolor mouse models, we briefly mention other animal and cellular models (zebrafish, chicken, drosophila, iPSC) that also rely on these constructs. Then, we highlight practical applications of multicolor mouse models to better understand organogenesis at single progenitor scale (clonal analyses) in the brain and briefly in several other tissues (intestine, skin, vascular, hematopoietic and immune systems). In addition, we detail the critical contribution of multicolor fate mapping strategies in apprehending the fine cellular choreography underlying tissue morphogenesis in several models with a particular focus on brain cytoarchitecture in health and diseases. Finally, we present the latest technological advances in multichannel and in-depth imaging, and automated analyses that enable to better exploit the large amount of data generated from multicolored tissues. Springer International Publishing 2022-02-20 2022 /pmc/articles/PMC8858928/ /pubmed/35187598 http://dx.doi.org/10.1007/s00018-021-04077-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Dumas, L. Clavreul, S. Michon, F. Loulier, K. Multicolor strategies for investigating clonal expansion and tissue plasticity |
title | Multicolor strategies for investigating clonal expansion and tissue plasticity |
title_full | Multicolor strategies for investigating clonal expansion and tissue plasticity |
title_fullStr | Multicolor strategies for investigating clonal expansion and tissue plasticity |
title_full_unstemmed | Multicolor strategies for investigating clonal expansion and tissue plasticity |
title_short | Multicolor strategies for investigating clonal expansion and tissue plasticity |
title_sort | multicolor strategies for investigating clonal expansion and tissue plasticity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858928/ https://www.ncbi.nlm.nih.gov/pubmed/35187598 http://dx.doi.org/10.1007/s00018-021-04077-1 |
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