RESUMEN
In this study we investigated the effect of systemic aminoglycoside administration on the expression of sialoglycoconjugates in the outer hair cell (OHC) glycocalyx of the adult guinea pig. Sialoglycoconjugates were visualized by means of ultrastructural lectin cytochemistry, using Limax flavus agglutinin (LFA) and wheat germ agglutinin (WGA) as probes. Labelling densities were determined for the apical membranes (including the stereocilia and stereociliary cross-links) and basolateral membranes of OHCs in the respective (basal, middle and apical) cochlear turns from animals that had been treated with gentamicin or neomycin for 5 or 15 consecutive days. Our results indicate that: (1) sialoglycoconjugate expression in the OHC glycocalyx demonstrates an intracochlear gradient decreasing towards the apical turn; (2) OHCs demonstrate a polarity in sialoglycoconjugate expression, in that the basolateral membranes contain more sialoglycoconjugates per surface area than the apical membranes; (3) aminoglycoside administration results in reduced expression of sialoglycoconjugates in the OHC glycocalyx; in this respect, basal-turn OHCs are more susceptible than those in the middle and apical turns; (4) reduction in sialoglycoconjugate expression after aminoglycoside administration is more prominent in the basolateral membranes; and (5) the difference in ototoxic potencies between gentamicin and neomycin is not reflected at the level of sialoglycoconjugate expression. The present data support our earlier hypothesis that aminoglycosides, already at an early phase of intoxication, interfere with the function of the endoplasmic reticulum and/or the Golgi apparatus, implying that these organelles play a crucial role in the initial phase of aminoglycoside-induced OHC degeneration.
Asunto(s)
Aminoglicósidos/toxicidad , Antibacterianos/toxicidad , Glicocálix/metabolismo , Células Ciliadas Auditivas Externas/efectos de los fármacos , Sialoglicoproteínas/metabolismo , Aminoglicósidos/administración & dosificación , Animales , Antibacterianos/administración & dosificación , Retículo Endoplásmico/metabolismo , Femenino , Gentamicinas/administración & dosificación , Gentamicinas/toxicidad , Glicocálix/efectos de los fármacos , Cobayas , Células Ciliadas Auditivas Externas/metabolismo , Células Ciliadas Auditivas Externas/ultraestructura , Histocitoquímica , Inyecciones Intraperitoneales , Lectinas/química , Neomicina/administración & dosificación , Neomicina/toxicidadRESUMEN
The histogenesis of early putative preneoplastic lesions, arising in exocrine pancreas of Syrian hamsters after treatment with N-nitrosobis(2-oxopropyl) amine (BOP), was evaluated using electron microscopy and immunohistochemistry. Electron microscopical examination of pseudoductular lesions, present in hamster pancreas 2-4 mo after treatment with BOP, demonstrated that acinar cells forming part of these lesions frequently lose their zymogen granules. However, convincing evidence of dedifferentiation of acinar cells to proliferating ductal/ductular cells was not found. Most ductal/ductular cells of the BOP-induced pseudoductular lesions stained positively with cytokeratins specific to ductal/ductular cells. Acinar cells were all negative and, moreover, those lining the pseudoductular lesions were frequently surrounded by cytoplasmic processes of adjacent cells that stained strongly positive with the cytokeratin antibody. The present findings indicate that the early pseudoductular lesions, induced in exocrine pancreas of hamsters by BOP, originate from proliferating ductal/ductular rather than proliferating dedifferentiated acinar cells.
Asunto(s)
Nitrosaminas , Enfermedades Pancreáticas/inducido químicamente , Lesiones Precancerosas/inducido químicamente , Animales , Cricetinae , Inmunohistoquímica , Masculino , Mesocricetus , Microscopía Electrónica , Páncreas/patología , Páncreas/ultraestructura , Enfermedades Pancreáticas/metabolismo , Enfermedades Pancreáticas/patología , Lesiones Precancerosas/metabolismo , Lesiones Precancerosas/patología , Valores de ReferenciaRESUMEN
The structure and organization of paired lymphoid tissue in the nasal mucosa, situated in the transitional zone on both sides of the septal opening of the pharyngeal duct, of conventionally-housed rats was examined by light microscopy and scanning and transmission electron microscopy. Each lymphoid structure consisted of follicles containing T- and B-cell areas, and was covered with specialized epithelium. This epithelium consisted of cuboidal ciliated cells with oval nuclei parallel to the basal lamina. Goblet cells were sparse. Occasionally, islands of microvilli-bearing cells (so called membraneous or M cells) covered the lymphoid structures. M Cells were also found as single cells among the ciliated cells. The morphological characteristics and the particular localization justify the conclusion that the nasal lymphoid tissue described belongs to the mucosa-associated lymphoid tissue. It is therefore suggested that this nasal structure be designated nasal lymphoid tissue.
Asunto(s)
Tejido Linfoide/citología , Nariz/citología , Animales , Células Epiteliales , Epitelio/ultraestructura , Tejido Linfoide/ultraestructura , Masculino , Microscopía Electrónica , Membrana Mucosa/citología , Membrana Mucosa/ultraestructura , Nariz/ultraestructura , Faringe/citología , Ratas , Ratas EndogámicasRESUMEN
The distribution of nerve fibres in the mucosa of the nasal septum of the rat was investigated by means of transmission electron microscopy on transverse and tangential ultrathin sections. Near the basement membrane of respiratory and squamous epithelium, a rather dense network of unmyelinated nerve fibres occurs. Some fibres in the respiratory epithelium ascend between the epithelial cells to reach up to the tight junctions. These fibres appeared in transverse sections to end as hooks or boutons, sometimes with branches. These shapes resemble the free nerve endings that are considered to act as nociceptors. The small intraepithelial fibres, with diameters of about 0.5-1 microns, contain both dense granules and clear vesicles comparable to synaptic vesicles. Substance P was found in dense granules in basal fibres; vasoactive intestinal peptide was absent throughout the epithelium. Acetylcholinesterase activity was observed closely associated with the basal fibres; the apical fibres showed little if any activity. Membrane specializations pointing to an efferent function as well as structures usually associated with mechanoreceptive functions were lacking in both respiratory and squamous epithelium.
Asunto(s)
Tabique Nasal/inervación , Terminaciones Nerviosas/ultraestructura , Acetilcolinesterasa/análisis , Animales , Axones/ultraestructura , Péptido Relacionado con Gen de Calcitonina/análisis , Epitelio/inervación , Epitelio/ultraestructura , Masculino , Microscopía Electrónica , Mucosa Nasal/inervación , Mucosa Nasal/ultraestructura , Tabique Nasal/ultraestructura , Terminaciones Nerviosas/química , Fibras Nerviosas/fisiología , Fibras Nerviosas/ultraestructura , Proteínas del Tejido Nervioso/análisis , Ratas , Sensación , Estrés Mecánico , Sustancia P/análisis , Péptido Intestinal Vasoactivo/análisisRESUMEN
The dye-coupled intercellular communication across gap junctions in primary hamster tracheal epithelial cells has been studied in serum-free, hormone-supplemented medium. In the absence of vitamin A, non-cytotoxic concentrations of cigarette-smoke condensate (CSC) inhibited intercellular communication between tracheal epithelial cells in a concentration-dependent way. All-trans retinol and retinoic acid showed biphasic effects on intercellular communication depending on their concentration. Physiological concentrations of retinol and retinoic acid increased the dye-coupled transfer of Lucifer Yellow CH via gap junctions compared with the dimethylsulfoxide-treated tracheal epithelial cells. At pharmacological concentrations retinol slightly increased the intercellular communication in the first 2 h of the exposure period, whereas upon longer treatment times with retinol and retinoic acid, gap-junction-mediated intercellular communication was inhibited almost completely. When retinol was given to tracheal epithelial cells before exposure to CSC or simultaneously with CSC-exposure, retinol counteracted the inhibitory potential of CSC on intercellular communication. The results of the present study clearly indicate that both CSC and all-trans retinol influence the intercellular communication between primary hamster tracheal epithelial cells in serum-free, hormone-supplemented culture medium.