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1.
Somatosens Mot Res ; 19(3): 213-7, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12396578

RESUMEN

To clarify the role of neurotrophin receptors in the development of Ruffini endings, periodontal ligaments and trigeminal ganglia of trkA, trkB, and trkC knockout mice were immunostained for protein gene product 9.5 (PGP 9.5), calcitonin gene-related peptide (CGRP), parvalbumin (PV), and calretinin (CR). Innervation patterns of PGP 9.5- and CGRP-immunoreactive fibers were examined in the periodontal ligament of the knockout mice. PGP 9.5-positive fibers in the incisal periodontal ligaments of trkA and trkC knockout mice form Ruffini endings distinguished by dendritic ramifications and branches. However, Ruffini endings were not present in the periodontal ligament of trkB knockout mice. Only free nerve endings were observed in tissue of trkB knockout mice. Compared with trkA and trkC knockouts, the proportion of CR-positive neurons in mandibular and maxillary regions of the trigeminal ganglion of trkB knockout mice is decreased. These findings indicate that the development of periodontal Ruffini endings is regulated by trkB-dependent and CR-coexpressing neurons.


Asunto(s)
Mecanorreceptores/fisiología , Ligamento Periodontal/inervación , Receptor trkB/fisiología , Animales , Péptido Relacionado con Gen de Calcitonina/metabolismo , Mecanorreceptores/anomalías , Mecanorreceptores/ultraestructura , Ratones , Ratones Noqueados/genética , Terminaciones Nerviosas/ultraestructura , Fibras Nerviosas/fisiología , Ligamento Periodontal/metabolismo , Receptor trkA/deficiencia , Receptor trkA/genética , Receptor trkB/deficiencia , Receptor trkB/genética , Receptor trkC/deficiencia , Receptor trkC/genética , Tioléster Hidrolasas/metabolismo , Ubiquitina Tiolesterasa
2.
Mol Genet Genomics ; 266(4): 572-83, 2001 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11810228

RESUMEN

In Drosophila melanogaster, segment identity is determined by specific expression of homeotic genes (Hox). The Hox expression pattern is first initiated by gap and pair-rule genes and then maintained by genes of the Polycomb-group (Pc-G) and the trithorax-group (trx-G). The corto gene is a putative regulator of the Hox genes since mutants exhibit homeotic transformations. We show here that, in addition to previously reported genetic interactions with the Pc-G genes Enhancer of zeste, Polycomb and polyhomeotic, mutations in corto enhance the extra-sex-comb phenotype of multi sex combs, Polycomb-like and Sex combs on midleg. corto also genetically interacts with a number of trx-G genes (ash1, kismet, kohtalo, moira, osa, Trithorax-like and Vha55). The interactions with genes of the trx-G lead to phenotypes displayed in the wing, in the postpronotum or in the thoracic mechanosensory bristles. In addition, we analyzed the regulation of the Hox gene Ultrabithorax (Ubx) in corto mutants. Our results provide evidence that corto maintains the anterior border of Ubx expression in third-instar larvae. We suggest that this regulation is accomplished through an interaction with the products of the Pc-G and trx-G genes.


Asunto(s)
Tipificación del Cuerpo/genética , Proteínas de Unión al ADN/genética , Proteínas de Drosophila , Drosophila/embriología , Drosophila/genética , Genes de Insecto , Factores de Transcripción , Animales , Genes Homeobox , Proteínas de Homeodominio/genética , Proteínas de Insectos/genética , Larva , Masculino , Mecanorreceptores/anomalías , Mutación , Fenotipo , Complejo Represivo Polycomb 1 , Alas de Animales/anomalías
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