Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “GANGLION”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 883 records · Page 49Linked to original sources

Pattern formation in the retinal ganglion cell layer and visual brain centres.

Development of adult patterns of cell distribution in the retinal ganglion cell layer from an approximately even initial topography are described for frogs and mammals. An area centralis and visual streak form in the frog only after metamorphosis, probably by the greater addition of cells to the ciliary margin nasally and temporally than dorsally and ventrally. By contrast, in mammals all cells destined to occupy the ganglion cell layer are generated before the area centralis and visual streak are formed. Patterns of cell death seem unlikely to explain changing cells distributions within the ganglion cell population and we are currently documenting patterns of cell migration to address this issue. The formation of specific connections between retinal ganglion cells and their partner cells in the brains of lower vertebrates is also discussed. At stages before optic axon outgrowth the eye already contains positional information to determine formation of appropriate central connections. Optic nerve regeneration studies in frogs indicate that positional cues are available in visual centres. However, interactions between fibres can overwhelm any such cues, allowing an orderly shift in connections to accommodate changes in the relative numbers of ganglion cells and their partner cells in the brain. Thus in the frog, retinotopicity is maintained during the postmetamorphic increase in ganglion cell number associated with area centralis and visual streak formation, despite an absence of central cell division. Similarly, an entire visual field in time becomes represented in an orderly fashion within the remaining portion of a partially ablated mature visual centre. Interactions between fibres are also considered responsible for the formation of ocular dominance columns, such as those found in binocular regions of the mammalian visual cortex. The role of visual experience is usually to refine and maintain the precise patterns of connectivity established by ontogenetic mechanisms.

Animals↗

Ganglion cell death in glaucoma: pathology recapitulates ontogeny.

I review some improvements in our knowledge about the death of retinal ganglion cells in glaucoma during the last 20 years. These include the realisation that glaucoma damage precedes its detection by perimetry, the fact that the lamina cribrosa is a major site of axonal injury to ganglion cells, and the association between regional structure of optic nerve head connective tissue and the pattern of glaucoma damage. The selective susceptibility of larger retinal ganglion cells and its functional significance are described. Apoptosis is the mode of cell death in at least some ganglion cells in experimental glaucoma. This supports a theory that retrograde axonal transport failure leads to loss of trophic factor influence on ganglion cells, causing them to initiate their own suicide. As a consequence of this theory, two therapeutic avenues are suggested for prevention of glaucoma injury and cell death: delivery of trophic factors and manipulation of ganglion cell genetic expression of controlling influences over programmed cell death.

Apoptosis↗

Number, distribution and size of retinal ganglion cells in the jungle crow (Corvus macrorhynchos).

A retinal ganglion cell density map was generated using Nissl-stained retinal whole mounts from the jungle crow (Corvus macrorhynchos). The total number, distribution and size of these cells were determined in the area centralis, as well as in temporal, nasal, dorsal and ventral retinal regions. The mean total number of ganglion cells was estimated to be 3.6 x 10(6). The highest densities were found in the area centralis (25 600 /mm2) and the dorso-temporal part of the retina, suggesting the highest quality of vision. This density diminished nearly concentrically from the central area towards the retinal periphery. The number of ganglion cells was highest in the temporal retina followed, in order, by the nasal, dorsal and ventral retinal regions. Based on ganglion cell size, the retina seemed to consist of the following five regions: central, temporal, nasal, dorsal and ventral. Ganglion cell size ranged from 16 to 288 microm2, with smaller cells predominating in central regions above the optic disc and larger cells comprising more of the peripheral regions. The present study showed two highly populated areas of ganglion cells in the crow retina and it is expected that the crow retina provides well-developed monocular and binocular vision.

Animals↗

Long-term survival of retinal ganglion cells following optic nerve section in adult bcl-2 transgenic mice.

The bcl-2 gene codes for a protein that acts as a powerful inhibitor of active cell death. Since the transection of the optic nerve in adult mammalians starts a massive process of degeneration in retinal ganglion cells, we investigated whether the overexpression of bcl-2 in adult transgenic mice can protect the axotomized ganglion cells. We performed intracranial optic nerve transection on both wild type and transgenic adult mice, and we tested cell survival 2 or 3.5 months after axotomy. The percentage of surviving ganglion cells after optic nerve section was computed by combining the counts of the optic nerve fibres in intact nerves with the cell density measures of the ganglion cell layer of axotomized retinae. From these data we found that in transgenic mice approximately 65% of ganglion cells survived 3.5 months after axotomy. In contrast, 2 months after surgery, < 10% of ganglion cells were left in wild type retinae. We have also examined the morphology and fine structure of the proximal stump of the sectioned optic nerves by light and electron microscopy. In the transgenic mice a very large number of axons survived after surgery and they still exhibited fairly normal morphology and ultrastructure. On the other hand the wild type transected nerves had only a few visible axons that displayed clear signs of degeneration. We conclude that the overexpression of Bcl-2 protein in central neurons is a very effective strategy to ensure long-term survival in axotomized cells.

Animals↗

Age-dependent changes in the regulation mechanisms for intracellular calcium ions in ganglion cells of the mouse retina.

The purpose of this study was to investigate the role of intracellular calcium buffering in retinal ganglion cells. We performed a quantitative analysis of calcium homeostasis in ganglion cells of early postnatal and adult mice by simultaneous patch-clamp recordings in sliced tissue and microfluorometric calcium measurements with Fura-2. Endogenous calcium homeostasis was quantified by using the 'added buffer' approach which uses amplitudes and decay time constants of calcium transients to give a standard for intracellular calcium buffering. The recovery phase of depolarization-induced calcium transients was well approximated by a mono-exponential function with a decay time constant that showed a linear dependence on dye concentration. Endogenous calcium binding ratios were found to be 575 (n = 18 cells) in early postnatal and 121 (n = 18 cells) in adult retinal ganglion cells. With respect to ganglion cell degeneration at early postnatal stages, our measurements suggest that neuroprotection of a majority of developing ganglion cells partially results from a specialized calcium homeostasis based on high buffering capacities. Furthermore, the dramatic decrease of the intracellular calcium buffering capacity during ganglion cell development may enhance their vulnerability to neurodegeneration.

Aging↗

Axonal conduction velocities of functionally characterized retinal ganglion cells in goldfish.

1. Visual response properties and conduction velocities of retinal ganglion cells were studied by extracellular recordings in the intact goldfish eye. Visually responsive single units were confirmed as ganglion cells by collision testing, and their receptive fields were mapped. 2. From compound action potentials, we identified groups I-V in the optic nerve, with overall conduction velocities of 11.5 +/- 1.17, 7.1 +/- 0.79, 4.4 +/- 0.56, 3.1 +/- 0.31 and 2.3 +/- 0.18 m s-1 (mean +/- S.D.) at 23 degrees C. 3. Ganglion cells were classified by their receptive fields as off-, on-off- or on-centre. Nearly all confirmed ganglion cells had axonal conduction velocities in groups II, III and IV; none fell in the fastest group, I. 4. Off-centre ganglion cells had conduction velocities only in the fast group, II. On-off-centre cells fell mainly in group III, with some in group, II. On-centre cells fell in groups II-V, but mainly in groups III and IV. 5. Receptive field centre diameters were 5-30 deg measured with a photopic background. The mean diameters for off-, on-off- and on-centres were 24, 15 and 18 deg, respectively. The relatively larger diameter and higher rate of spontaneous firing of the off-centre cells were maintained under different adaptation conditions. 6. The off-centre cells can be identified with an anatomical class of large, alpha-like ganglion cells in the goldfish retina.

Action Potentials↗

The action of morphine on the superior cervical ganglion and on the nictitating membrane of the cat.

The intravenous injection of 0.05 to 2.5 mg. of morphine reduced the response of the nictitating membrane in the cat to pre- and post-ganglionic stimulation. This inhibitory action of morphine was due neither to inhibition of ganglionic transmission nor to a depressant action on the smooth muscle of the nictitating membrane. It is suggested that morphine inhibits the release of the sympathetic transmitter from the postganglionic nerve endings.Small amounts of morphine (5 to 20 mug.) injected intravenously reduced or abolished the contraction of the nictitating membrane due to the injection of histamine, pilocarpine and 5-HT into the arterial blood supply of the superior cervical ganglion. This inhibitory action of morphine was due to an action on the ganglion cells, since such small amounts of morphine did not reduce the response of the nictitating membrane to postganglionic stimulation. Similar amounts of morphine did not abolish the stimulation of the ganglion by nicotine, tetramethylammonium and potassium chloride.The results provide further evidence for the view that histamine, pilocarpine, and 5-hydroxytryptamine have no "nicotine-like" properties but act on receptors of the ganglion cells different from the acetylcholine receptors.

Animals↗

Action of some ganglion-stimulating substances on the secretion of saliva from the submandibular gland.

An attempt has been made to determine whether the ganglionic actions of pilocarpine and of 4-(m-chlorophenylcarbamoyloxy)-2-butynyltrimethylammonium chloride (McN-A-343) contribute to their effect on salivary secretion. Salivary flow was measured from the submandibular glands of spinal cats. Destruction of the superior cervical ganglion and adrenalectomy failed to reduce the stimulant effect of pilocarpine and McN-A-343. Substances known to interfere with the ganglionic actions of pilocarpine (cocaine, methadone and choline 2:6-xylyl ether bromide) likewise failed to modify the response. It is concluded that stimulation of autonomic ganglia and of the adrenal medulla does not contribute to the salivary secretion observed after intravenous injections of pilocarpine and of McN-A-343. Dimethylphenylpiperazinium, a nicotine-like ganglion-stimulating substance, causes salivary flow by stimulating the adrenal medulla as well as parasympathetic ganglion cells; stimulation of the superior cervical ganglion by this substance does not contribute to the salivary response.

(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethy↗

The release of acetylcholine by acetylcholine in the cat's superior cervical ganglion.

1. The experiments described in this paper tested the effect of acetylcholine (ACh), carbachol or preganglionic nerve stimulation on the release of ACh from the cat's perfused superior cervical ganglion; radioactive tracer methods were used.2. When the ganglion's transmitter store of ACh had been labelled, radioactive ACh was released by nerve stimulation (5 Hz for 2 min), but there was no release by ACh (0.15-15 mug) or by carbachol (1-10 mug) when these drugs were injected close to the ganglion. Perfusion with low or moderate concentrations of ACh (0.15-5 mug/ml) also failed to release ACh, but high concentrations (15-50 mug/ml) released a small amount of labelled material. There was no correlation between ganglion stimulation by ACh and release of radioactivity.3. Ganglion-blocking concentrations of ACh did not reduce the release of ACh during continuous nerve stimulation.4. When resting (unstimulated) ganglia were perfused with (3)H-choline and eserine, the extra ACh synthesized and stored by such ganglia (surplus ACh) was labelled. Preganglionic nerve stimulation (5 Hz for 2 min) did not release surplus ACh, but perfusion with ACh (0.5-15 mug/ml), or injection of carbachol (0.5-2.5 mug) did.5. Surplus ACh released by ACh or by carbachol did not contribute to the ganglion stimulating effect of either drug.6. It is concluded that the presynaptic effects of ACh are not of physiological importance.

Acetylcholine↗

Pharmacological studies on the hypogastric ganglion of the rat and guinea-pig.

1. Preparations were developed whereby the hypogastric ganglion of the rat or guinea-pig was perfused through its vasculature with saline solutions. Drugs were injected into the perfusion stream, and their effects were indicated by contractions of the vas deferens. The base of this organ could be ligated to prevent the drugs reaching the smooth muscle via the blood vessels. For comparison, experiments were also performed on fully isolated preparations of the rat and guinea-pig hypogastric nerve-vas deferens, where the vas deferens was held in an inner bath, so that drugs added to the outer bath could act only on the ganglion. Attempts were made to demonstrate non-nicotinic receptors in these preparations.2. It was shown that the perfused hypogastric ganglion of the guinea-pig would respond repeatedly to several nicotinic stimulants, though autodesensitization eventually occurred. The fully isolated preparation behaved similarly, but desensitized much more rapidly. In contrast, the rat ganglion, either perfused or fully isolated, was remarkably insensitive to nicotinic stimulant drugs.3. Neither species responded well to non-nicotinic stimulants; that from the guinea-pig gave small contractions to methacholine in about 33% of cases, but did not respond to (4-m-chlorophenyl-carbamoyloxy)-2-butynyl trimethylammonium chloride (McN-A-343). With the rat, the situation was opposite.4. The guinea-pig ganglion did not become more sensitive to non-nicotinic stimulants after some treatments known to sensitize the cat superior cervical ganglion. These include preganglionic tetanization, chronic decentralization, and removal of all potassium. Sensitization did occur, however, in the presence of physostigmine, after tachyphylaxis to dimethyl phenyl piperazinium iodide (DMPP) had developed, and when the preparation was perfused with a suspension of washed erythrocytes.5. It is concluded that the responses of sympathetic ganglia vary from one species to another, and according to whether the organs are perfused or fully isolated.

Animals↗

Evidence that the 5-HT3 receptors of the rat, mouse and guinea-pig superior cervical ganglion may be different.

1. Using grease-gap recordings from the isolated superior cervical ganglion of mouse, rat and guinea-pig, we have compared the depolarization evoked by 5-hydroxytryptamine (5-HT) with that evoked by the selective 5-HT3 receptor agonist 2-methyl-5-HT (2-Me-5-HT). 2. The maximum depolarization induced by 2-Me-5-HT was smaller than that induced by 5-HT in all three species, and particularly in the guinea-pig. 3. The 5-HT2 receptor antagonist ketanserin (1 microM) caused a clear rightward shift of the dose-response curve to 5-HT on the guinea-pig ganglion, but not on the mouse or rat ganglion. Spiperone (0.03 microM) had a quantitatively similar action to ketanserin (0.1 microM) on the 5-HT dose-response curve of the guinea-pig ganglion. Ketanserin had no significant effect on the dose-response curve to 2-Me-5-HT on any of these ganglia. 4. Using 2-Me-5-HT as the agonist, we determined the pA2 values for two 5-HT3 receptor antagonists. The potency of ICS 205-930 varied by approximately 100 fold between the species and that of (+)-tubocurarine varied by over 1000 fold. The differences in the pA2 values of these compounds varied independently among the species. 5. We conclude that 5-HT3 receptors are present on the superior cervical ganglion from the rat, mouse and guinea-pig, but these receptors may be pharmacologically distinct from each other. In addition, the depolarization of the guinea-pig superior cervical ganglion by low concentrations of 5-HT is largely mediated by ketanserin-sensitive receptors.

Animals↗

The effects of selective stellate ganglion manipulation on ventricular refractoriness and excitability.

The effects of selective stellate ganglion stimulation or stellectomy on ventricular excitability were studied in 30 open chest mongrel dogs anesthetized with alpha-chloralose. The effective refractory period (ERP) and strength interval curves (stimulus intensity [S2] = twice the diastolic threshold [ERP], and 2, 3, 5, 7, and 14 mA) were determined using bipolar epicardial electrodes placed in the mid-anterior wall of the right ventricle (RV) and the mid-posterolateral wall of the left ventricle (LV) during left stellate ganglion stimulation (LSGSt, n = 8) or right stellate ganglion stimulation (RSGSt, n = 8), or after left stellectomy (LSGEx, n = 7) or right stellectomy (RSGEx, n = 7). LSGEx prolonged ERP-LV (172 +/- 9 vs 167 +/- 8 msec, P < 0.05) and ERP-RV (163 +/- 10 vs 158 +/- 14 msec, P < 0.05). RSGEx prolonged ERP-LV (168 +/- 17 vs 162 +/- 15 msec, P < 0.01) and ERP-RV (166 +/- 14 vs 160 +/- 13 msec, P < 0.01), and the times of the strength interval curves obtained for each S2 intensity in both ventricles. LSGSt decreased ERP-LV (157 +/- 11 vs 163 +/- 12 msec, P < 0.01) and ERP-RV (147 +/- 18 vs 157 +/- 17 msec, P < 0.05), and the times of the strength interval curves obtained for each S2 intensity in both ventricles. RSGSt did not significantly decreased ERP-LV (152 +/- 11 vs 156 +/- 9 msec); however, it significantly shortened the times of the strength interval curves obtained for S2 intensities of 2 and 7 mA in the LV, and shortened ERP-RV (139 +/- 10 vs 145 +/- 7 msec, P < 0.01) and the times of the strength interval curve for S2 intensities of 2, 3, and 5 mA in the RV. A significant interaction (MANOVA test) was observed between the ventricle studied and the ganglion stimulated for S2 intensities of 2 and 3 mA, and between the effect of stimulation and the ganglion stimulated for S2 intensities of 3 and 14 mA. To conclude, selective stellectomy prolonged epicardial ventricular refractoriness in both the mid-anterior wall of the RV and the mid-posterolateral wall of the LV; the magnitude of the epicardial excitability variations in both areas was different during selective stellate ganglion stimulation.

Analysis of Variance↗

Strychnine blocks transient but not sustained inhibition in mudpuppy retinal ganglion cells.

Transient and sustained inhibitory synaptic inputs to on-centre, off-centre, and on-off ganglion cells in the mudpuppy retina were studied using intracellular recording in the superfused eye-cup preparation. When chemical transmission was blocked with 4 mM-Co2+, application of either glycine or gamma-aminobutyric acid (GABA) caused a hyperpolarization and conductance increase in all ganglion cells. For both amino acids, the responses were dose dependent in the range 0.05-10 mM, with a half-maximal response at about 0.7 mM. Glycine and GABA sensitivities were very similar in all three types of ganglion cells. The response to applied glycine was selectively antagonized by 10(-5) M-strychnine and the response to applied GABA was selectively antagonized by 10(-5) M-picrotoxin. In all ganglion cells, 10(-5) M-strychnine eliminated the transient inhibitory events which occur at the onset and termination of a light stimulus. The block of transient inhibition was associated with a relative depolarization of membrane potential and decrease in conductance at these times. Strychnine had no effect on membrane potential or conductance in darkness or during sustained inhibitory responses to light. Picrotoxin (10(-5) M) did not block transient inhibitory events in any ganglion cells, but did affect other components of their responses. The results suggest that in all three classes of ganglion cells transient inhibition, but not sustained inhibition, may be mediated by glycine or a closely related substance.

Animals↗

Glutamate receptors of ganglion cells in the rabbit retina: evidence for glutamate as a bipolar cell transmitter.

1. Intracellular and extracellular recordings were obtained from ganglion cells in the rabbit retina. The effects of glutamate analogues and antagonists were studied using a perfusion method for drug application. 2. Kainate (KA) excited all ganglion cells directly and caused a large increase in firing rate. N-Methyl-DL-aspartate (NMDLA) also excited ganglion cells but it was less potent and caused burst firing. 3. Quisqualate (QQ) and (RS)-2-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA) excited many ganglion cells and were approximately as potent as KA. Less frequently, QQ and AMPA had inhibitory effects possibly due to polysynaptic action. 4. General glutamate antagonists such as cis-2,3-piperidine dicarboxylic acid (PDA) and kynurenic acid blocked the light input to all ganglion cells. PDA and kynurenic acid blocked the effects of KA and NMDLA, but not carbachol, indicating that they act as glutamate antagonists in the rabbit retina. Kynurenic acid did not block the excitatory action of QQ, even though light responses were abolished. 5. Amacrine cells were depolarized by KA or QQ and less potently by NMDLA. Their light-evoked responses were blocked by PDA. 6. We conclude that the light input to ganglion cells in the rabbit retina is predominantly mediated by KA receptors. This is consistent with the idea that 'on' and 'off' bipolar cells are excitatory and release glutamate.

Action Potentials↗

Amplitude and phase of responses of macaque retinal ganglion cells to flickering stimuli.

1. We have measured responses of macaque retinal ganglion cells to a uniform flickering field, with variation in luminance, chromaticity or both (heterochromatic flicker). 2. With heterochromatic flicker, as the luminance ratio of the flicker components was varied, phasic ganglion cell activity went through a minimum and an abrupt phase change close to equal luminance. Tonic ganglion cell responses underwent a gradual phase change without any minimum close to equal luminance. For red on-centre cells, when wavelengths above 570 nm were altered with white, a progressive phase advance occurred as luminance ratio (L lambda/LW) was increased. With wavelengths below 570 nm a progressive phase lag occurred. For green on-centre cells, the opposite pattern was found. For all tonic cells, the higher the temporal frequency, the more rapidly did such phase changes occur. A simple model incorporating a centre-surround delay of 3-8 ms could quantitatively account for these changes. 3. With luminance flicker of different dominant wavelengths, amplitudes and phase of responses of phasic ganglion cells were independent of wavelength at all frequencies. The amplitude and phase of the responses of tonic ganglion cells was very dependent on wavelength, as well as on flicker frequency. Their characteristics hardly ever resembled results from phasic cells. 4. For achromatic flicker, response phase of tonic cells at or above 10 Hz was variable, probably due to the centre-surround delay. Such variability was not seen among phasic cells. 5. An interesting implication of these results is that the ability of tonic ganglion cells to unambiguously signal rapid chromatic or spatial change is limited.

Animals↗

Concomitant activation of two types of glutamate receptor mediates excitation of salamander retinal ganglion cells.

1. Cells in the ganglion cell layer of salamander retinal slices were voltage clamped using patch pipettes. Light elicited transient excitatory postsynaptic currents (EPSCs) in on-off ganglion cells and sustained EPSCs in on ganglion cells. Light-evoked inhibitory postsynaptic currents in these cells could be blocked by 100 microM-bicuculline methobromide and 500 nM-strychnine. 2. In the presence of external Cd2+, at a concentration that blocked light-evoked synaptic inputs, N-methyl-D-aspartate (NMDA) and the non-NMDA-receptor agonists, quisqualate and kainate, gated conductances in both on-off and on ganglion cells. The current-voltage (I-V) curve for the conductance elicited by NMDA had a negative slope between -40 and -70 mV and a reversal potential near 0 mV. The I-V curves for the non-NMDA-receptor-mediated conductances were nearly linear and also had reversal potentials near 0 mV. 3. I-V curves were measured at an early time point near the peak of transient EPSCs and at a later time point during the decay phase of the responses. The late I-V curve had a negative slope below -40 mV. The early I-V curve had a positive slope over the entire voltage range but the slope was greater at positive than at negative potentials. The evoked current reversed near 0 mV at both time points. 4. The region of negative slope of the late I-V curve was eliminated when Mg2+ was removed from the external saline. A slowly decaying component of transient EPSCs was eliminated in 20 microM-DL-2-amino-7-phosphonoheptanoate (AP7), an NMDA-receptor antagonist. 5. Application of 1 microM-6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), a non-NMDA-receptor antagonist at this concentration, blocked a fast component of transient EPSCs. 6. Our results demonstrate that the synaptic inputs to on-off ganglion cells have two components: a slower NMDA-receptor-mediated component having a time-to-peak of 110 +/- 45 ms and an e-fold decay time of 209 +/- 35 ms at -31 mV (mean +/- S.D., n = 5), and a faster non-NMDA-receptor-mediated component having a time-to-peak of 28 +/- 10 ms and an e-fold decay time of 43 +/- 20 ms at -31 mV (n = 8). 7. A similar analysis of sustained EPSCs of on ganglion cells showed that these currents resulted from sustained activation of both NMDA and non-NMDA receptors.

Ambystoma↗

Frequency map of the spiral ganglion in the cat.

A frequency map of the cat spiral ganglion has been determined on the basis of reconstructed cochleas in which individual spiral ganglion cells were labeled with horseradish peroxidase following determination of their characteristic frequency; the cochleas were the same as those used by Liberman and Oliver [J. Comp. Neurol. 223, 163-176 (1984)]. By matching this map to one previously described for the organ of Corti [M. C. Liberman, J. Acoust. Soc. Am. 72, 1441-1449 (1982)], an estimate of the afferent innervation density of the inner hair cells was derived. Counts of myelinated nerve fibers at the habenula perforata and inner hair cells were also performed and yielded similar results in all but the most basal 10%-15% of the cochlea. Between 0.1 and 20 kHz there is a gradual monotonic increase as a function of frequency in the number of spiral ganglion cells terminating on each inner hair cell, from about eight ganglion cells per inner hair cell to about 30 ganglion cells per inner hair cell. Above 20 kHz, it seems there is a decrease to about ten ganglion cells per inner hair cell. The greatest innervation density is at approximately the region of the basilar membrane with the greatest density of inner hair cells per millimeter.

Animals↗

Trigeminal ganglion infection by thymidine kinase-negative mutants of herpes simplex virus after in vivo complementation.

Infection of trigeminal ganglion by herpes simplex virus (HSV) thymidine kinase-negative (TK-) mutants was investigated in mixed infection studies in mice. Mice were corneally inoculated with TK- HSV alone or with mixtures of TK- HSV-TK+ HSV. When inoculated alone, an arabinosylthymine-selected HSV type 1 TK- mutant and a HSV type 2 TK- deletion mutant infected mouse ocular tissues but rarely infected ganglion tissues. However, both TK- mutants readily infected ganglion tissues when they were inoculated in mixtures with TK+ HSV. By means of mixed infection studies, it was demonstrated that TK- HSV could readily establish acute and latent ganglion infections. It was thought that the frequent infection of trigeminal ganglion tissue by both TK- mutants after mixed TK(-)-TK+ HSV infection was the result of in vivo complementation. After mixed TK(-)-TK+ HSV infection and subsequent cultivation of ganglion explants in arabinosylthymine, results supported the conclusion that when TK- was present in ganglia it was in the same neurons that contained TK+ HSV.

Animals↗