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1.
Methods Mol Biol ; 1891: 201-219, 2019.
Article de Anglais | MEDLINE | ID: mdl-30414135

RÉSUMÉ

Modulation of bone morphogenetic protein (BMP) activity is essential to the progression of limb development in the mouse embryo. Genetic disruption of BMP signaling at various stages of limb development causes defects ranging from complete limb agenesis to oligodactyly, polydactyly, webbing, and chondrodysplasia. To probe the state of BMP signaling in early limb buds, we designed two sets of primers to measure both spatially and quantitatively the transcription of nine key genes indicative of canonical BMP activity. One set is used to generate digoxigenin (DIG)-labeled antisense RNA probes for whole-mount mRNA in situ hybridization, while the second set is used for SYBR® Green-based quantitative PCR on limb bud cDNA. Here we describe step-by-step protocols for both methods around this specific set of genes.


Sujet(s)
Protéines morphogénétiques osseuses/métabolisme , Bourgeons de membre/embryologie , Bourgeons de membre/métabolisme , Animaux , Protéines morphogénétiques osseuses/génétique , Régulation de l'expression des gènes au cours du développement , Hybridation in situ , Souris , Réaction de polymérisation en chaine en temps réel , Transduction du signal
2.
PLoS One ; 10(4): e0123186, 2015.
Article de Anglais | MEDLINE | ID: mdl-25923915

RÉSUMÉ

We have modified and optimized the technique of organotypic slice culture in order to study the mechanisms regulating growth and pattern formation in regenerating axolotl limb blastemas. Blastema cells maintain many of the behaviors that are characteristic of blastemas in vivo when cultured as slices in vitro, including rates of proliferation that are comparable to what has been reported in vivo. Because the blastema slices can be cultured in basal medium without fetal bovine serum, it was possible to test the response of blastema cells to signaling molecules present in serum, as well as those produced by nerves. We also were able to investigate the response of blastema cells to experimentally regulated changes in BMP signaling. Blastema cells responded to all of these signals by increasing the rate of proliferation and the level of expression of the blastema marker gene, Prrx-1. The organotypic slice culture model provides the opportunity to identify and characterize the spatial and temporal co-regulation of pathways in order to induce and enhance a regenerative response.


Sujet(s)
Protéine morphogénétique osseuse de type 2/pharmacologie , Bourgeons de membre/effets des médicaments et des substances chimiques , Tissu nerveux/cytologie , Ambystoma mexicanum , Animaux , Prolifération cellulaire/effets des médicaments et des substances chimiques , Techniques de coculture , Régulation de l'expression des gènes/effets des médicaments et des substances chimiques , Protéines à homéodomaine/métabolisme , Humains , Immunohistochimie , Techniques in vitro , Bourgeons de membre/cytologie , Bourgeons de membre/métabolisme , Cellules souches mésenchymateuses/cytologie , Cellules souches mésenchymateuses/effets des médicaments et des substances chimiques , Cellules souches mésenchymateuses/métabolisme , Tissu nerveux/métabolisme , Pyrazoles/pharmacologie , Pyrimidines/pharmacologie , Protéines Smad/métabolisme
3.
Dev Dyn ; 236(1): 321-31, 2007 Jan.
Article de Anglais | MEDLINE | ID: mdl-17117438

RÉSUMÉ

Molecular mechanisms patterning the tetrapod limb, including anterior-posterior axis determination involving Sonic hedgehog (Shh), have received much attention, particularly in amniotes. Anterior-posterior patterning in urodele amphibians differs radically from that of amniotes in that it shows a pronounced anterior-to-posterior sequence of digit development. In contrast, amniotes develop their digits almost simultaneously with a slight posterior-to-anterior polarity. Here we use cyclopamine, an inhibitor of the Hedgehog signaling pathway, to investigate the role of Shh in anterior-posterior patterning in the urodele limb. Inhibition of Shh signal transduction affects digit number long before their morphological appearance. In accordance with the apparently derived order of digit development in urodeles, exposure reproducibly removes digits in a posterior-to-anterior sequence, the inverse of their developmental sequence. This pattern of digit loss mimics the order of digit loss in natural variation. We suggest that variation in Shh expression and/or signal transmission may explain natural variation in digit number in urodeles.


Sujet(s)
Plan d'organisation du corps , Membres/embryologie , Protéines Hedgehog/physiologie , Transduction du signal , Ambystoma mexicanum , Animaux , Protéines Hedgehog/antagonistes et inhibiteurs , Bourgeons de membre/embryologie , Bourgeons de membre/métabolisme , Phénotype , Phylogenèse , Alcaloïdes de Veratrum/pharmacologie
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