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Biomedical subjects

A Sans

Publications and source records attributed to A Sans.

At least 73 records · Page 4Linked to original sources
PubMed1989

Ultrastructural study of striated organelles in vestibular sensory cells of human fetuses.

The presence of striated organelles in the vestibular receptor of human fetuses of 10 to 22 weeks gestation was investigated. They were very frequent under the cuticular plate of the sensory cells, especially in type-I hair cells. Cross-sections of striated organelles showed that there were twice as many filaments in the dark bands as in the light bands. These filaments were often arranged in broken lines. Striated organelles were frequently associated with microtubules, mitochondria, and endoplasmic reticulum, and were fused with the plasma membrane forming an incomplete ring in the cytoplasm of the cells. We discuss the possibility that in adults, these striated organelles participate in an active mechanism that regulates the transduction of stimuli by means of a feedback control of the apical part of the calyx.

Age Factors↗
PubMed1989

Short latency vestibular potentials evoked by electrical round window stimulation in the guinea pig.

Short-latency potentials evoked by round window electrical stimulation were recorded in guinea pig by means of vertex-pinna skin electrodes using averaging techniques. Constant current shocks of 20 microseconds or 50 microseconds (25-300 microA) were used to evoke both auditory and vestibular brain-stem potentials. Pure auditory potentials, comparable to those evoked by acoustic clicks, were obtained by 20 microseconds electrical stimuli and disappeared during an auditory masking procedure made with a continuous white noise (110 dB SPL). Short latency potentials labeled V1, V2 and V3 were obtained by 50 microseconds electrical stimuli during an auditory masking procedure. This response disappeared after specific vestibular neurectomy, whereas the auditory response evoked by acoustic clicks or by electrical stimulation remained unchanged, suggesting that these latter potentials had a vestibular origin.

Animals↗
PubMed1989

Vestibular hair cells isolated from guinea pig labyrinth.

Living sensory cells were isolated from the cristae ampullaris and macula utriculi of the guinea pig. Enzymatic and mechanical dissociation were used to obtain different populations of hair cells, the most predominant being type I cells. Their form varied: cell body of variable roundness, and neck and cilia of different lengths. The observation of many tilted cuticular plates supports the hypothesis of active mechanisms regulating mechanotransduction at the apex of these cells. Cell viability was verified by double fluorescent labeling (FDA-PI), which indicated that under correct conditions about 90% of the sensory cells could be maintained in vitro for several hours after dissociation. The detection of actin in the cuticular plate and cilia shows that the technique has various potential applications in morphological studies, and can contribute to investigations on the physiology of mammalian vestibular cells.

Animals↗
PubMed1988

Alpha-fodrin (brain spectrin) immunocytochemical localization in rat vestibular hair cells.

The presence of a spectrin-related protein in rat vestibular sensory receptors was demonstrated by immunocytochemistry and immunoblotting using affinity purified anti alpha-fodrin antibodies. Intense immunoreactivity was found in the apical pole of sensory hair cells where it seems to be concentrated in the cuticular plate. In contrast, alpha-fodrin immunoreactivity was absent from the stereocilia. We suggest that a spectrin-related protein participates in the organization of the cuticular plate of vestibular hair cells by cross-linking actin filaments as well as by anchoring the cuticular plate to the apical cell membrane.

Animals↗
PubMed1988

Appearance and distribution of neuron-specific enolase and calbindin (CaBP 28 kDa) in the developing human inner ear.

The onset and development of neuron-specific enolase (NSE) and calbindin immunoreactivities were studied in the inner ear of human fetuses aged from 6-7 to 14 weeks of gestation. NSE occurred very early in ganglion neurons. Its appearance in vestibular sensory cells at 8 weeks coincided with the formation of the first afferent synapses, and showed an apex/base gradient in the cristae. Calbindin was found in vestibular ganglion neurons at 6-7 weeks and in the cochlear ganglion neurons at 8-9 weeks. Vestibular sensory cells and the whole ventral wall of the cochlear duct were stained from 8-9 weeks. At 14 weeks, calbindin staining occurred only in the sensory cells of the cochlear neuroepithelium. Non-neuronal secretory structures, i.e. Kölliker's organ and some cells of the transitional zone of the utricle, were also reactive. Staining appeared in Kölliker's organ with a base to apex gradient and disappeared from it with an internal to external gradient. Calbindin appeared in vestibular sensory cells later than NSE staining, synapse formation and sensory hair bundle differentiation. By contrast in the cochlea, calbindin staining appeared in the neuroepithelium before sensory cell differentiation, but remained only in the hair cells after they had differentiated and been contacted by the afferent fibers.

Antibodies↗
PubMed1988

Early innervation and differentiation of hair cells in the vestibular epithelia of mouse embryos: SEM and TEM study.

Early afferent innervation and differentiation of sensory vestibular cells were studied in mouse embryos from gestation day (GD) 13 to 16. Afferent neurites were found as early as GD 13 in the epithelium when there were no clearly differentiated sensory cells. By GD 14 the earliest sensory cells which exhibited short hair bundles at their luminal pole were then contacted by afferent endings at their basal part. On GD 15 nerve endings establishing specialized synaptic contacts, characterized by asymmetrical membrane densities and synaptic bodies, were observed. At this stage, microtubules contacting the presynaptic membranes, as well as coated vesicles were found. On GD 16 the hair cells were multi-afferented and numerous synaptic bodies were found. These results showing a concomitance between the hair cell differentiation and the establishment of nerve contacts are discussed with particular respect to nerve-hair cell interactions during sensory differentiation. This study does not point to a primary induction of vestibular hair cell differentiation by nerve endings, but it is consistent with the possibility that the ingrowth of nerve fibers is one of many factors that influence the differentiation of receptor cells. With respect to synapse formation, it is assumed that the location of synaptic bodies at presynaptic densities is determined by the arrival of afferent nerve endings.

Animals↗
PubMed1988

Duplex-Doppler ultrasonography in monitoring clinical pancreas transplantation.

The findings are reported that were obtained with duplex-Doppler ultrasonography (US) in seven diabetic patients who underwent pancreatic grafting with pancreaticocystostomy. Five normal functioning grafts showed homogenous echostructure and pulsed Doppler spectrum characteristics of low impedance vascular beds. Four of these patients developed graft rejection (five episodes). The remaining two grafts had pulsed Doppler evidence of venous thrombosis. It was not possible to differentiate graft rejection from venous thrombosis using real-time US. In both circumstances a heterogeneous pancreatic echostructure with a small amount of peripancreatic fluid and an increase in pancreas size were observed. Pulsed Doppler, however, showed absence of venous flow in both cases of venous thrombosis whereas all rejection episodes were characterized by an increase in arterial impedance. We conclude that duplex-Doppler US is a promising noninvasive method of detecting surgical complications and graft rejection in pancreatic transplant recipients.

Adult↗
PubMed1988

Calbindin (CaBP 28 kDa) localization in the peripheral vestibular system of various vertebrates.

Previous reports on calbindin, a 28 kDa vitamin D-induced calcium-binding protein, located in the mammalian peripheral vestibular system indicated that it is specifically distributed and postulated that it could play a role in the electrophysiological functioning of the sensory cells. This immunocytochemical investigation of the distribution of calbindin in the vestibular system of various vertebrates: fishes (goldfish and sea-perch), amphibia (frog), birds (chicken) and mammals (mouse, cat and baboon), was performed to verify these observations. In the vestibular ganglion, only a few neurons were faintly immunoreactive in the fishes and the frog, while the staining was more intense but still not present in all neurons of the chicken, the mouse and the cat. All the neurons were immunoreactive in the baboon. No immunoreactivity was observed in the sensory epithelia of the fishes. All hair cells were strongly immunoreactive in the frog. In the other species, most of the hair cells in the cristae were immunostained except those situated in the peripheral areas. In the maculae, the hair cells of the striola were either the only ones stained or were more intensely stained or were more intensely stained than the others. The localization of calbindin in specific cellular types and its increasing abundance from the fishes to the mammals suggest that calbindin is associated with the capacity of sensory and nerve cells to analyze precise mechanical or biochemical stimulations.

Animals↗
PubMed1988

Secretory function of the vestibular nerve calyx suggested by presence of vesicles, synapsin I, and synaptophysin.

Type I sensory hair cells of the vestibular epithelium are nearly completely ensheathed by an afferent nerve ending, the vestibular nerve calyx. We have recently reported that the nerve calyx, and, in particular, its apical portions surrounding the neck of the hair cell, are immunoreactive for synapsin I (Favre et al., 1986), a major membrane component of small synaptic vesicles of axonal endings. We have now found, by electron microscopy, that the same region of the calyx is densely populated by microvesicles morphologically similar to typical presynaptic small synaptic vesicles. Furthermore, we have established by light microscopy immunocytochemistry that this region of the calyx also contains a high concentration of synaptophysin, another well-characterized major component of small synaptic vesicle membranes. These results suggest that the upper portion of the calyx is equipped with the machinery that in presynaptic terminals is involved in the release of neurotransmitters and raise the possibility that the calyx, via secretion of neurotransmitterlike substances, might modulate the function of type I hair cells.

Animals↗
PubMed1987

Immuno-electronmicroscopic localization of 'vitamin D-dependent' calcium-binding protein (CaBP-28k) in the vestibular hair cells of the cat.

The PAP immunohistochemical method was used to carry out a light- and electronmicroscopic study of the distribution of the vitamin D-dependent calcium-binding protein (CaBP-28k, calbindin, cholecalcin) in the vestibule of the young cat. It was found that the two types of hair cells, types I and II, were stained differently. Type II cells were intensely immunoreactive and their staining did not vary with the location of the cells within the crista ampullaris. Type I cells at the top of the cristae were lightly stained, or unstained, while the type I cells laterally or basally were frequently intensely stained. The nerve fibers arriving at the top of the cristae are highly immunoreactive while the fibers of the base are not stained. Immunostaining for CaBP was correlated with differences in the innervation of hair cells at the top and base of the cristae. This differential CaBP-immunostaining may reflect differences in the physiological activity of the cells. The electronmicroscopic study showed that CaBP is present throughout the cytoplasm of the hair cells but that its concentration was particularly high in the cuticular plate and stereocilia. This specific intracellular distribution of CaBP is discussed with the possible role of Ca2+ in the physiology of the vestibular hair cells.

Animals↗
PubMed1987

Afferent nerve ending development and synaptogenesis in the vestibular epithelium of human fetuses.

Synaptogenesis has been investigated in the vestibular epithelium of human fetuses aged from 7 to 14 weeks of gestation. The arrival of afferent nerve endings in the epithelium preceded hair cell differentiation. Synaptogenesis involved the proliferation of synaptic bodies. It was concomitant with the formation of contacts between microtubules and the presynaptic membrane, and the presence of numerous coated vesicles within the presynaptic area.

Cell Differentiation↗
PubMed1987

Immunohistochemical identification of neuron-specific enolase and calbindin in the vestibular receptors of human fetuses.

Immunohistochemical techniques were used to identify neuron-specific enolase (NSE) and calbindin in the vestibular receptors and ganglia of human fetuses at 10 weeks of gestation. NSE was found in vestibular ganglion cells and in a few sensory cells. The pattern of immunoreactivity in the sensory epithelia was characteristic of the appearance of NSE in these structures. Calbindin was found in vestibular ganglion cells and sensory cells which displayed a strong immunoreactivity. These findings are discussed with regard to synaptogenesis and they indicate that the vestibular receptors show biochemical signs of maturation consistent with the possibility of synaptic activity.

Calbindins↗
PubMed1987

Lactate dehydrogenase activity and its isoenzymes in concentric layers of adult bovine and calf lenses.

The activity of lactate dehydrogenase (LDH) and its isoenzyme pattern were studied in four concentric layers of adult bovine and calf lenses. In both groups the specific activity of the total LDH diminished progressively toward the internal nuclear layer; the decrease was greater in the adult lenses. The enzyme activities in the cortical layers of the calf lens were lower than in the adult lens, but in the inner nuclear layers, the opposite was found. All of the 5 LDH isoenzymes were found in each layer. In both groups of animals the LDH1 isoenzyme prevailed, followed by LDH2. No differences were found in the percentage of each isoenzyme in the different lens layers. The differences in the activitie(s) of LDH found may be due to post-translational or post-synthetic modifications which may occur during the aging process.

Aging↗
PubMed1987

[8 cases of diphtheria observed in Guadeloupe from 1979 to 1984].

From 1979 to 1984, 8 cases of diphtheria were diagnosed in Basse-Terre, in children aged 11 months to 6 years. All of them were badly or not vaccinated at all. They showed the common clinical features; two patients had only pharyngitis. Corynebacterium diphtheriae was isolated from the throat in 6 patients. All children were successfully treated by early administration of antitoxin and antibiotics.

Child↗
PubMed1986

Differentiation and maturation of the sensory hair bundles in the fetal and postnatal vestibular receptors of the mouse: a scanning electron microscopy study.

By means of scanning electron microscopy, the differentiation and maturation of sensory hair bundles have been studied in the ampullar cristae of the mouse during development from gestational day 13 (GD13) to postnatal day 10 (PD10). Two gradients of ciliary differentiation were demonstrated, one from the apex to the base and the other from the center to the periphery. The different hair bundles that appeared on the crista during the fetal period originated in an initial ciliary stage found in regions undergoing differentiation, differentiation, which was visible at the apex of the crista starting on GD14. This stage of ciliary development is gradually followed by a juvenile one at GD15. Starting on GD18, the maturation of hair bundles in the central apical area differed from that in the peripheral areas and prefigured the regional specialization of the crista found in the adult stage. In the discussion, we suggest that when the vestibular epithelial cells begin to exhibit ciliary differentiation, they are simultaneously contacted by nerve fibers.

Animals↗