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Closed Access item Snail family members and cell survival in physiological and pathological cleft palates

Authors:Martínez-Álvarez, Concepción
Blanco Fernández de Valderrama, María José
Pérez, Raquel
Rabadán, M. Angeles
Aparicio, Marta
Resel, Eva
Martínez, Tamara
Nieto, M. Ángela
Keywords:TGF-β3, TGF-β1, Palate development, Snail, Slug, Mouse, Chick, Epithelial–mesenchymal transition, Cell death, Survival
Issue Date:1-Jan-2004
Publisher:Elsevier
Citation:Developmental Biology 265(1): 207-218 (2004)
Abstract:Palate fusion is a complex process that involves the coordination of a series of cellular changes including cell death and epithelial to mesenchymal transition (EMT). Since members of the Snail family of zinc-finger regulators are involved in both triggering of the EMT and cell survival, we decided to study their putative role in palatal fusion. Furthermore, Snail genes are induced by transforming growth factor β gene (TGF-β) superfamily members, and TGF-β3 null mutant mice (TGF-β3−/−) show a cleft palate phenotype. Here we show that in the wild-type mouse at the time of fusion, Snail is expressed in a few cells of the midline epithelial seam (MES), compatible with a role in triggering of the EMT in a small subpopulation of the MES. We also find an intriguing relationship between the expression of Snail family members and cell survival associated to the cleft palate condition. Indeed, Snail is expressed in the medial edge epithelial (MEE) cells in TGF-β3−/−mouse embryo palates, where it is activated by the aberrant expression of its inducer, TGF-β1, in the underlying mesenchyme. In contrast to Snail-deficient wild-type pre-adhesion MEE cells, Snail-expressing TGF-β3 mutant MEE cells survive as they do their counterparts in the chick embryo. Interestingly, Slug is the Snail family member expressed in the chick MEE, providing another example of interchange of Snail and Slug expression between avian and mammalian embryos. We propose that in the absence of TGF-β3, TGF-β1 is upregulated in the mesenchyme, and that in both physiological (avian) and pathological (TGF-β3−/−mammalian) cleft palates, it induces the expression of Snail genes promoting the survival of the MEE cells and permitting their subsequent differentiation into keratinized stratified epithelium.
Description:12 páginas, 7 figuras.
Publisher version (URL):http://dx.doi.org/10.1016/j.ydbio.2003.09.022
URI:http://hdl.handle.net/10261/32355
ISSN:0012-1606
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Appears in Collections:(IC) Artículos

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