RESUMEN
Globular star clusters are compact and massive stellar systems old enough to have witnessed the entire history of our Galaxy, the Milky Way. Although recent results suggest that their formation may have been more complex than previously thought, they still are the best approximation to a stellar population formed over a relatively short timescale (less than 1 Gyr) and with virtually no dispersion in the iron content. Indeed, only one cluster-like system (omega Centauri) in the Galactic halo is known to have multiple stellar populations with a significant spread in iron abundance and age. Similar findings in the Galactic bulge have been hampered by the obscuration arising from thick and varying layers of interstellar dust. Here we report that Terzan 5, a globular-cluster-like system in the Galactic bulge, has two stellar populations with different iron contents and ages. Terzan 5 could be the surviving remnant of one of the primordial building blocks that are thought to merge and form galaxy bulges.
RESUMEN
MATERIALS AND METHODS: Ten human healthy teeth were extracted for orthodontic or surgical purposes and processed for histological and immunocytochemical examination with the streptavidin-biotin-peroxidase method. Highly purified antibodies were used to reveal the distribution of intermediate filaments (vimentin, desmin, alpha-smooth muscle actin), histiocytic antigens (alpha-1-antitrypsin, lysozyme), neural and neural-crest-associated antigens (neuron-specific enolase, chromogranin-A, S-100, synaptophysin, glial fibrillary acidic protein, neurofilaments) in the adult pulp tissue. RESULTS: Vimentin immunostaining was strongly positive in the network of pulpal fibroblasts. Desmin and alpha-smooth muscle actin were present only in the vessel walls. Staining for alpha-1-antitrypsin and lysozyme reveals a number of macrophage-like cells in the central portion of the pulp. Macrophages were the most dominating immunocompetent cells. Negative immunostaining for chromogranin-A demonstrated the absence of neuroendocrine antigens in the adult dental pulp. Immunostaining for neuron-specific enolase, S-100 protein, synaptophysin, glial fibrillary acidic protein and neurofilaments were positive, with different intensity, in nerve fibres, but no pulp cell was found to be immunoreactive. CONCLUSIONS: The conclusion is drawn that the lack of labelling of pulp cells by the neural associated antibodies could be due to differentiation processes during tissue development.
Asunto(s)
Antígenos/metabolismo , Pulpa Dental/metabolismo , Histiocitos/inmunología , Filamentos Intermedios/metabolismo , Cresta Neural/inmunología , Adulto , Diente Premolar , Diente Canino , Pulpa Dental/inmunología , Humanos , Inmunohistoquímica , Persona de Mediana EdadRESUMEN
Morphogenesis and cell differentiation in the developing tooth are controlled by a series of reciprocal interactions between the epithelial and mesenchymal tissues. The exact molecular mechanisms operating in these interactions are unknown at present, but both structural components of the extracellular matrix and cellular receptors have been suggested to be involved. In this review we resume our knowledge about tenascin and syndecan distribution and activity.