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The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model
The Notch pathway is an ancient, evolutionary conserved intercellular signaling mechanism that is involved in cell fate specification and proper embryonic development. The Jagged2 gene, which encodes a ligand for the Notch family of receptors, is expressed from the earliest stages of odontogenesis i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277265/ https://www.ncbi.nlm.nih.gov/pubmed/37330998 http://dx.doi.org/10.1007/s00018-023-04831-7 |
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author | Mitsiadis, Thimios A. Pagella, Pierfrancesco Capellini, Terence D. Smith, Moya Meredith |
author_facet | Mitsiadis, Thimios A. Pagella, Pierfrancesco Capellini, Terence D. Smith, Moya Meredith |
author_sort | Mitsiadis, Thimios A. |
collection | PubMed |
description | The Notch pathway is an ancient, evolutionary conserved intercellular signaling mechanism that is involved in cell fate specification and proper embryonic development. The Jagged2 gene, which encodes a ligand for the Notch family of receptors, is expressed from the earliest stages of odontogenesis in epithelial cells that will later generate the enamel-producing ameloblasts. Homozygous Jagged2 mutant mice exhibit abnormal tooth morphology and impaired enamel deposition. Enamel composition and structure in mammals are tightly linked to the enamel organ that represents an evolutionary unit formed by distinct dental epithelial cell types. The physical cooperativity between Notch ligands and receptors suggests that Jagged2 deletion could alter the expression profile of Notch receptors, thus modifying the whole Notch signaling cascade in cells within the enamel organ. Indeed, both Notch1 and Notch2 expression are severely disturbed in the enamel organ of Jagged2 mutant teeth. It appears that the deregulation of the Notch signaling cascade reverts the evolutionary path generating dental structures more reminiscent of the enameloid of fishes rather than of mammalian enamel. Loss of interactions between Notch and Jagged proteins may initiate the suppression of complementary dental epithelial cell fates acquired during evolution. We propose that the increased number of Notch homologues in metazoa enabled incipient sister cell types to form and maintain distinctive cell fates within organs and tissues along evolution. |
format | Online Article Text |
id | pubmed-10277265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-102772652023-06-20 The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model Mitsiadis, Thimios A. Pagella, Pierfrancesco Capellini, Terence D. Smith, Moya Meredith Cell Mol Life Sci Visions and Reflections The Notch pathway is an ancient, evolutionary conserved intercellular signaling mechanism that is involved in cell fate specification and proper embryonic development. The Jagged2 gene, which encodes a ligand for the Notch family of receptors, is expressed from the earliest stages of odontogenesis in epithelial cells that will later generate the enamel-producing ameloblasts. Homozygous Jagged2 mutant mice exhibit abnormal tooth morphology and impaired enamel deposition. Enamel composition and structure in mammals are tightly linked to the enamel organ that represents an evolutionary unit formed by distinct dental epithelial cell types. The physical cooperativity between Notch ligands and receptors suggests that Jagged2 deletion could alter the expression profile of Notch receptors, thus modifying the whole Notch signaling cascade in cells within the enamel organ. Indeed, both Notch1 and Notch2 expression are severely disturbed in the enamel organ of Jagged2 mutant teeth. It appears that the deregulation of the Notch signaling cascade reverts the evolutionary path generating dental structures more reminiscent of the enameloid of fishes rather than of mammalian enamel. Loss of interactions between Notch and Jagged proteins may initiate the suppression of complementary dental epithelial cell fates acquired during evolution. We propose that the increased number of Notch homologues in metazoa enabled incipient sister cell types to form and maintain distinctive cell fates within organs and tissues along evolution. Springer International Publishing 2023-06-18 2023 /pmc/articles/PMC10277265/ /pubmed/37330998 http://dx.doi.org/10.1007/s00018-023-04831-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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 | Visions and Reflections Mitsiadis, Thimios A. Pagella, Pierfrancesco Capellini, Terence D. Smith, Moya Meredith The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title | The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title_full | The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title_fullStr | The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title_full_unstemmed | The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title_short | The Notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
title_sort | notch-mediated circuitry in the evolution and generation of new cell lineages: the tooth model |
topic | Visions and Reflections |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277265/ https://www.ncbi.nlm.nih.gov/pubmed/37330998 http://dx.doi.org/10.1007/s00018-023-04831-7 |
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