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Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix
Interdigital cell death is a physiological regression process responsible for sculpturing the digits in the embryonic vertebrate limb. Changes in the intensity of this degenerative process account for the different patterns of interdigital webbing among vertebrate species. Here, we show that Reelin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789180/ https://www.ncbi.nlm.nih.gov/pubmed/24030152 http://dx.doi.org/10.1038/cddis.2013.322 |
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author | Díaz-Mendoza, M J Lorda-Diez, C I Montero, J A García-Porrero, J A Hurlé, J M |
author_facet | Díaz-Mendoza, M J Lorda-Diez, C I Montero, J A García-Porrero, J A Hurlé, J M |
author_sort | Díaz-Mendoza, M J |
collection | PubMed |
description | Interdigital cell death is a physiological regression process responsible for sculpturing the digits in the embryonic vertebrate limb. Changes in the intensity of this degenerative process account for the different patterns of interdigital webbing among vertebrate species. Here, we show that Reelin is present in the extracellular matrix of the interdigital mesoderm of chick and mouse embryos during the developmental stages of digit formation. Reelin is a large extracellular glycoprotein which has important functions in the developing nervous system, including neuronal survival; however, the significance of Reelin in other systems has received very little attention. We show that reelin expression becomes intensely downregulated in both the chick and mouse interdigits preceding the establishment of the areas of interdigital cell death. Furthermore, fibroblast growth factors, which are cell survival signals for the interdigital mesoderm, intensely upregulated reelin expression, while BMPs, which are proapototic signals, downregulate its expression in the interdigit. Gene silencing experiments of reelin gene or its intracellular effector Dab-1 confirmed the implication of Reelin signaling as a survival factor for the limb undifferentiated mesoderm. We found that Reelin activates canonical survival pathways in the limb mesoderm involving protein kinase B and focal adhesion kinase. Our findings support that Reelin plays a role in interdigital cell death, and suggests that anoikis (apoptosis secondary to loss of cell adhesion) may be involved in this process. |
format | Online Article Text |
id | pubmed-3789180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37891802013-10-18 Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix Díaz-Mendoza, M J Lorda-Diez, C I Montero, J A García-Porrero, J A Hurlé, J M Cell Death Dis Original Article Interdigital cell death is a physiological regression process responsible for sculpturing the digits in the embryonic vertebrate limb. Changes in the intensity of this degenerative process account for the different patterns of interdigital webbing among vertebrate species. Here, we show that Reelin is present in the extracellular matrix of the interdigital mesoderm of chick and mouse embryos during the developmental stages of digit formation. Reelin is a large extracellular glycoprotein which has important functions in the developing nervous system, including neuronal survival; however, the significance of Reelin in other systems has received very little attention. We show that reelin expression becomes intensely downregulated in both the chick and mouse interdigits preceding the establishment of the areas of interdigital cell death. Furthermore, fibroblast growth factors, which are cell survival signals for the interdigital mesoderm, intensely upregulated reelin expression, while BMPs, which are proapototic signals, downregulate its expression in the interdigit. Gene silencing experiments of reelin gene or its intracellular effector Dab-1 confirmed the implication of Reelin signaling as a survival factor for the limb undifferentiated mesoderm. We found that Reelin activates canonical survival pathways in the limb mesoderm involving protein kinase B and focal adhesion kinase. Our findings support that Reelin plays a role in interdigital cell death, and suggests that anoikis (apoptosis secondary to loss of cell adhesion) may be involved in this process. Nature Publishing Group 2013-09 2013-09-12 /pmc/articles/PMC3789180/ /pubmed/24030152 http://dx.doi.org/10.1038/cddis.2013.322 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Díaz-Mendoza, M J Lorda-Diez, C I Montero, J A García-Porrero, J A Hurlé, J M Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title | Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title_full | Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title_fullStr | Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title_full_unstemmed | Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title_short | Interdigital cell death in the embryonic limb is associated with depletion of Reelin in the extracellular matrix |
title_sort | interdigital cell death in the embryonic limb is associated with depletion of reelin in the extracellular matrix |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789180/ https://www.ncbi.nlm.nih.gov/pubmed/24030152 http://dx.doi.org/10.1038/cddis.2013.322 |
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