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1.
Dev Dyn ; 244(4): 577-90, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25645398

RESUMO

BACKGROUND: Intercellular communication by the hedgehog cell signaling pathway is necessary for tooth development throughout the vertebrates, but it remains unclear which specific developmental signals control cell behavior at different stages of odontogenesis. To address this issue, we have manipulated hedgehog activity during zebrafish tooth development and visualized the results using confocal microscopy. RESULTS: We first established that reporter lines for dlx2b, fli1, NF-κB, and prdm1a are markers for specific subsets of tooth germ tissues. We then blocked hedgehog signaling with cyclopamine and observed a reduction or elimination of the cranial neural crest derived dental papilla, which normally contains the cells that later give rise to dentin-producing odontoblasts. Upon further investigation, we observed that the dental papilla begins to form and then regresses in the absence of hedgehog signaling, through a mechanism unrelated to cell proliferation or apoptosis. We also found evidence of an isometric reduction in tooth size that correlates with the time of earliest hedgehog inhibition. CONCLUSIONS: We hypothesize that these results reveal a previously uncharacterized function of hedgehog signaling during tooth morphogenesis, regulating the number of cells in the dental papilla and thereby controlling tooth size.


Assuntos
Papila Dentária/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Proteínas Hedgehog/metabolismo , Odontoblastos/metabolismo , Dente/embriologia , Animais , Apoptose , Comunicação Celular , Proliferação de Células , Proteínas de Ligação a DNA/metabolismo , Proteínas de Fluorescência Verde/metabolismo , Proteínas de Homeodomínio/metabolismo , Microscopia de Fluorescência , Morfogênese , NF-kappa B/metabolismo , Proteínas Nucleares/metabolismo , Odontogênese/fisiologia , Fator 1 de Ligação ao Domínio I Regulador Positivo , Transdução de Sinais , Germe de Dente/embriologia , Fatores de Transcrição/metabolismo , Alcaloides de Veratrum/química , Peixe-Zebra/embriologia , Proteínas de Peixe-Zebra/metabolismo
2.
Evol Dev ; 15(2): 107-18, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-25098636

RESUMO

Teeth with two or more cusps have arisen independently from an ancestral unicuspid condition in a variety of vertebrate lineages, including sharks, teleost fishes, amphibians, lizards, and mammals. One potential explanation for the repeated origins of multicuspid teeth is the existence of multiple adaptive pathways leading to them, as suggested by their different uses in these lineages. Another is that the addition of cusps required only minor changes in genetic pathways regulating tooth development. Here we provide support for the latter hypothesis by demonstrating that manipulation of the levels of Fibroblast growth factor (Fgf) or Bone morphogenetic protein (Bmp) signaling produces bicuspid teeth in the zebrafish (Danio rerio), a species lacking multicuspid teeth in its ancestry. The generality of these results for teleosts is suggested by the conversion of unicuspid pharyngeal teeth into bicuspid teeth by similar manipulations of the Mexican Tetra (Astyanax mexicanus). That these manipulations also produced supernumerary teeth in both species supports previous suggestions of similarities in the molecular control of tooth and cusp number. We conclude that despite their apparent complexity, the evolutionary origin of multicuspid teeth is positively constrained, likely requiring only slight modifications of a pre-existing mechanism for patterning the number and spacing of individual teeth.


Assuntos
Evolução Molecular , Peixes/metabolismo , Transdução de Sinais , Dente/fisiologia , Animais , Proteínas Morfogenéticas Ósseas/metabolismo , Characidae/genética , Characidae/crescimento & desenvolvimento , Characidae/metabolismo , Fatores de Crescimento de Fibroblastos/metabolismo , Peixes/classificação , Peixes/genética , Pirazóis/farmacologia , Pirimidinas/farmacologia , Peixe-Zebra/genética , Peixe-Zebra/crescimento & desenvolvimento , Peixe-Zebra/metabolismo
3.
J Exp Zool B Mol Dev Evol ; 308(4): 442-53, 2007 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-17538949

RESUMO

The digestive tract of vertebrates is a complex organ system required for the digestion of food and the absorption of nutrients. The colon evolved as a water absorption organ essential for vertebrates to survive on land. In contrast to land vertebrates, the Chondrichthyes (sharks, skates and rays) are nearly iso-osmotic with their ocean environment and do not reabsorb water from food waste. To understand the origin of the vertebrate colon, we examined the distribution of sulfated and sialyated mucus-producing cells in the little skate, Raja erinacea, as an indication of water absorption function in the chondrichthian digestive tract. The percentage of acid mucin producing goblet cells was analyzed in the spiral valve and hindgut of little skate and the small intestine and colon of mouse embryos. Levels of acid mucins in the hindgut of the little skate was comparable to that of the small intestines of terrestrial vertebrates, whereas the distal region of the spiral valve contained high levels of acid mucin producing cells similar to the colon of mouse and chick. The low numbers of acid mucins in the little skate hindgut confirms that a functional colon for water absorption is absent in the Chondrichthyes. Interestingly, the presence of high levels of acid mucins in the posterior spiral valve provides evidence for a possible primordial water-absorbing organ in the elasmobranchs. Hoxd13 patterns acid mucins in the colons of terrestrial vertebrates. Expression of Hoxd13 and Hoxa13 in R. erinacea suggests conserved roles for Hox genes in patterning the early hindgut.


Assuntos
Trato Gastrointestinal/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Células Caliciformes/metabolismo , Proteínas de Homeodomínio/metabolismo , Mucinas/genética , Animais , Colo/embriologia , Colo/metabolismo , Trato Gastrointestinal/citologia , Trato Gastrointestinal/embriologia , Intestino Delgado/embriologia , Intestino Delgado/metabolismo , Camundongos , Rajidae/embriologia , Rajidae/genética
4.
J Neuroimmunol ; 186(1-2): 164-76, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17451814

RESUMO

We re-engineered the immunoglobulin rearrangements from clonally expanded CSF B cells of three Multiple Sclerosis patients as Fab fragments, and used three methods to test for their antigen (Ag) specificity. Nine out of ten Fab fragments were reactive to Myelin Basic Protein (MBP). The one Fab that did not react to MBP was a product of receptor editing. Two of the nine MBP reactive Fabs were also reactive to GFAP and CNPase, indicating that these clones were polyreactive. Targeting the mechanisms that allow these self-reactive B cells to reside in the CSF of MS patients may prove to be a potent immunotherapeutic strategy.


Assuntos
Autoantígenos/imunologia , Linfócitos B/imunologia , Fragmentos Fab das Imunoglobulinas/imunologia , Esclerose Múltipla Recidivante-Remitente/líquido cefalorraquidiano , Esclerose Múltipla Recidivante-Remitente/imunologia , Proteína Básica da Mielina/imunologia , Células Clonais/imunologia , Células Clonais/metabolismo , Ensaio de Imunoadsorção Enzimática/métodos , Citometria de Fluxo , Rearranjo Gênico do Linfócito B/fisiologia , Genes de Imunoglobulinas , Proteína Glial Fibrilar Ácida/metabolismo , Humanos , Fragmentos Fab das Imunoglobulinas/metabolismo , Imunoprecipitação , Modelos Imunológicos
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