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G M Shepherd

Publications and source records attributed to G M Shepherd.

At least 91 records · Page 5Linked to original sources
PubMed1991

Electrotonic structure of olfactory sensory neurons analyzed by intracellular and whole cell patch techniques.

1. Experimental studies employing whole cell patch recordings from freshly isolated olfactory sensory neurons of the salamander (Ambystoma tigrinum) yield much higher estimates of specific membrane resistance (Rm) than studies using conventional intracellular recordings from in situ neurons. Because Rm is critical for understanding information transfer in these cells, we have used computational methods to analyze the possible reasons for this difference. 2. Compartmental models were constructed for both the in situ and isolated neurons, using SABER, a general-purpose simulation program. For Rm in the in situ cell, we used a high value of 100,000 omega.cm2, as estimated in the whole cell recordings from isolated cells. A shunt across the cell membrane caused by the penetrating microelectrode was simulated by several types of shunt mechanisms, and its effects on lowering the apparent value of resting membrane potential (MP), input resistance (RN), and membrane time constant (tau m) and increasing the electrotonic length (L) were analyzed. 3. A good approximation of the electrotonic properties recorded intracellularly was obtained in the in situ model with high Rm combined with an electrode shunt consisting of Na and K conductances. A raised K conductance (1-5 nS) helps to maintain the resting MP while contributing to the increased conductance, which lowers RN and shortens the apparent tau m toward the experimental values. 4. Combined shunt resistances of 0.1-0.2 G omega (5-10 nS) gave the best fits with the experimental data. These shunts were two to three orders of magnitude smaller than the values reported from intracellular penetrations in muscle cells and motoneurons. This may be correlated with the smaller electrode tips used in the recordings from these small neurons. We thus confirm the prediction that even small values of electrode shunt have relatively large effects on the recorded electrotonic properties of small neurons, because of their high RN (2-5 G omega). 5. We have further explored the effects on electrotonic structure of a nonuniform Rm by giving higher Rm values to the distally located cilia compared with the proximal soma-dendritic region, as indicated by recent experiments. For the same RN, large increases in ciliary Rm above 100,000 omega.cm2 can be balanced by relatively small decreases below that value in soma-dendritic Rm. A high ciliary Rm appears to be a specialization for transduction of the sensory input, as reported also in photoreceptors and hair cells.

Ambystoma↗
PubMed1991

Single odor-sensitive channels in olfactory receptor neurons are also gated by cyclic nucleotides.

Olfactory transduction is thought to occur by processes that are mainly restricted to the specialized cilia emanating from the distal end of the receptor neuron's single dendrite. The involvement of a cAMP-based second messenger system seems likely, and a cyclic nucleotide-sensitive current has been recorded in patches of membrane from the cilia. However, the small diameter of the cilia and the high density of channels within the membrane limit the application of the patch recording technique in the cilia. We have found that the cAMP-sensitive channels also exist at a much lower density within the far more accessible dendritic membrane. Recording from on-cell patches, we have observed single-channel activity in response to extracellularly applied odor substances. The channels have a single-channel conductance of 40 pS and a reversal potential near 0 mV. These same channels are activated by treatments that elevate intracellular cyclic nucleotide concentrations. The results provide a direct demonstration that the cyclic nucleotide-gated channel is the conductance pathway for the odor-elicited current.

1-Methyl-3-isobutylxanthine↗
PubMed1991

Analysis of single cyclic nucleotide-gated channels in olfactory receptor cells.

In the accompanying article (Firestein et al., 1991b), we have demonstrated that odor- and cyclic nucleotide-sensitive channels exist at a low density in the dendritic membranes of isolated salamander olfactory receptor neurons. Here, we analyze the cyclic nucleotide sensitivity of these channels using the inside-out patch recording technique. Both cAMP and cGMP, at micromolar concentrations, are capable of inducing channel openings. The biophysical parameters of channel activity are nearly the same in response to either ligand. The unitary conductance is about 45 pS, the reversal potential of single-channel currents is +5 mV, and the I/V relation is linear over the range -80 to +80 mV. The channel activity shows no obvious voltage dependence in divalent cation-free symmetrical solutions. The channel shows no desensitization, even to agonist exposures lasting 15 sec. Mean open time is about 1.5 msec; the closed time distribution is best fit by two exponentials with a fast time constant in the submillisecond range (ca. 0.15 msec) and a slower time constant in the millisecond range (ca. 1.5 msec). The only clear difference in the activity of the two ligands is in their affinity constants. The K1/2 for cAMP is 20 microM; that for cGMP is 4 microM. In both cases, the Hill coefficient is greater than 2, suggesting that channel opening requires the cooperative action of three ligand molecules.

Animals↗
PubMed1991

Local information processing in dendritic trees: subsets of spines in granule cells of the mammalian olfactory bulb.

The anaxonic granule cell of the olfactory bulb is believed to inhibit mitral and tufted cells through reciprocal dendrodendritic synapses. However, little is known about the detailed input-output properties of the granule cell. This study explores the functional properties of granule cells by using detailed reconstructions of Golgi-impregnated granule cells as the basis for computational models. Three Golgi-impregnated granule cells from the olfactory bulbs of C57BL/6j mice were selected for detailed analysis. Measurements were made of the diameter and length of all spine heads, spine necks, and dendritic branches. These measurements formed the basis of a compartmental model of each cell in which simulations of the spread of synaptic potentials within the dendritic tree were performed with SABER (Analogy, Inc.), a circuit analysis program. The results show that the degree of spread of synaptic potentials can define functionally related subsets of spines within the dendritic tree. The size of these subsets varies with the anatomical location of the input spine, the magnitude of the input, the time course of the input, the size of the spine neck resistance, and the activity of other spines. The data indicate that the functional organization of granule cell dendritic arbors is more complex than previously thought: between the level of the individual spine and the entire dendritic tree are several levels of subsets of spines that can mediate discrete localized inhibition onto subsets of mitral or tufted cell secondary dendrites within the external plexiform layer of the olfactory bulb.

Animals↗
PubMed1990

Neuron simulations with SABER.

Computational models can provide critical tests of hypotheses of neuronal function. These models are essential for dealing with the complications of time- and voltage-dependent (active) ionic conductances. Commercial circuit analysis programs have been useful tools for this work. We report our experience modelling biophysically realistic membrane properties with SABER (Analogy, Inc.), a new general purpose simulator. SABER allows construction of models with arbitrary membrane properties. This is a major advantage over similar programs (e.g. SPICE), which are limited to a predefined library of electronic components. The empirically determined equations that describe rate constants, ionic conductances, currents, and concentration shifts can be translated directly into model elements ('templates') written in C-like code. We describe the development of SABER models that simulate a synapse and an action potential.

Action Potentials↗
PubMed1990

Actin cores of hair-cell stereocilia support myosin motility.

The actin cores of hair-cell stereocilia were tested as a substrate for the movement of myosin-coated beads in an in vitro assay. Large numbers of stereocilia from bullfrog sacculi and semicircular canals were isolated by blotting onto coverglasses and were demembranated to expose the polar actin tracks of their cytoskeletal cores. Silica or polystyrene beads, coated with thick filaments of chicken skeletal muscle myosin, were added to this core preparation in the presence of ATP. Myosin-coated beads could reach some of the cores by diffusion alone, but the efficiency and precision of the assay were improved considerably by the use of "optical tweezers" (a gradient-force optical trap) to deposit the beads directly on the cores. Beads applied in this fashion bound and moved unidirectionally at 1-2 microns/s, escaping the retarding force of the trap. Actin filaments within the stereocilia are cross-linked by fimbrin, but this did not appear to interfere with the motility of myosin. Beads coated with optic-lobe kinesin were also tested for movement; these bound and moved unidirectionally at 0.1-0.2 microns/s when applied to microtubule-based kinociliary cores, but not when applied to actin-based stereociliary cores. Our results are consistent with, and lend support to, a model for hair cell adaptation in which a molecular motor such as myosin maintains tension on the mechanically gated transduction channels. Optical tweezers and video-enhanced differential interference contrast optics provide high efficiency and improved optical resolution for the in vitro analysis of myosin motility.

Actins↗
PubMed1990

Time course of the membrane current underlying sensory transduction in salamander olfactory receptor neurones.

1. Odour elicited currents in freshly isolated olfactory receptor neurones were analysed using the whole-cell patch-clamp technique. Brief pulses (35-50 ms) and steps (100 ms-5 s) of odour solution were delivered by pressure ejection from a nearby micropipette. 2. Pulses of odour solution directed at the cell induced an inward depolarizing current of 50-750 pA leading to the generation of action potentials. The I-V relation for this current was linear over the range -60-(+)20 mV and showed a reversal potential of +5 mV. The magnitude of the current increased with stimulus strength, for a given pulse duration, over approximately one decade of concentration change. 3. Pulses of odour solution focally delivered to the cilia elicited a large response, but those directed toward the soma did not. Conversely pulses of K+ solution at the cilia failed to evoke any response while those directed at the dendrite and soma elicited an inward clamp current. This provides direct evidence that odour sensitivity is localized mainly to the cilia and possibly the distal dendrite. 4. The odour elicited current activated with a long latency of 150-600 ms after the odour solution arrived at the cell. This latency, as well as the time-to-peak and the rise half-time, were relatively independent of stimulus concentration, changing less than 25% over the entire concentration range of stimulus sensitivity. These observations are consistent with the participation of a second messenger system in olfactory transduction. 5. For brief stimulus pulses less than 100 ms, the stimulus diffused away before the odour response current reached its peak value, so that the peak and decay of the odour response occurred in the absence of significant odour stimulus. The time course of the current decay was fitted by a single exponential with a time constant that was concentration dependent, varying from 0.8 to 1.3 s. 6. For longer steps of stimulus presentation, up to 1 s, the magnitude of the response current became a function of the duration of the pulse as well as the stimulus concentration, indicating that the transduction process involved an integrating step. This is consistent with the idea that the odour elicited current is the result of the summation of many smaller unitary events. From responses to weak stimulation an integration period of 700-1000 ms was calculated. 7. During prolonged steps of maintained stimulus presentation (greater than 5 s) the odour elicited current was transient.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗
PubMed1990

T cell receptor variable gene expression: analysis in ragweed-sensitive patients during allergen exposure.

Four monoclonal antibodies (MAb) to V region determinants of the alpha/beta-chain of the T cell antigen receptor (TCR) were used, by cytofluorography, to detect discrete populations of peripheral blood T cells (PBT). Together they identify 10-15% of circulating CD3+ T cells. Each MAb is known to detect specific V regions of the beta-chain. Thus V beta 5 gene products are recognized by MAb C37, V beta 6 by OT145, V beta 8 by Ti3a, and V beta 12 by MAb S511. In previous studies, we found that the percentages of PBT detected by these MAb show little variation over time in normal individuals. In order to determine if there is a change in TCR V gene usage during an immune response to an environmental antigen, 12 atopic patients with known ragweed sensitivity by history and skin test were followed for a 6-month period encompassing the ragweed season. No shifts in V gene usage that could be correlated with the ragweed season were consistently observed. The patients could be arbitrarily divided into two groups: in group I little variation over time was observed in the T cell populations identified by the MAb used, while group II was characterized by marked variation of the same T cell populations over time. In group II individuals, the population of Ti3a+ T cells showed the most variation over time. Failure to observe shifts in PBT subpopulations, identified by expression of different TCR V regions, during exposure to an allergen to which an IgE response has been made may mean that such shifts do not occur or that they occur primarily at the tissue site of antigen exposure and not in the peripheral circulation or that they occur in T cell subpopulations not identified by the reagents used.

Adult↗
PubMed1989

"Bundle blot" purification and initial protein characterization of hair cell stereocilia.

Stereocilia were isolated from bullfrog (Rana catesbeiana) saccular hair cells by nitrocellulose adhesion. The high purity and high yield of the preparation were demonstrated by microscopy. SDS/PAGE of stereociliary proteins resolved 12-15 major bands. Actin, previously identified as a component of the stereociliary core, was identified in purified stereocilia as a band comigrating with authentic actin and by phalloidin labeling of intact isolated stereocilia. Fimbrin was identified in immunoblots of purified stereocilia. The most abundant other proteins migrated at 11, 14, 16-19, 27, and 36 kDa. Demembranated stereociliary cores consisted primarily of protein bands corresponding to actin and fimbrin and several proteins ranging from 43 to 63 kDa. Because the adaptation mechanism in hair cells is calcium-sensitive and seems localized to stereocilia, we sought evidence for calcium-binding proteins in stereocilia. Calmodulin and calbindin antibodies labeled stereocilia in intact cells. A protein band in purified stereocilia exhibited a Ca2+-dependent shift in electrophoretic mobility identical to that of authentic calmodulin, and the 27-kDa band may represent calbindin. These biochemical data demonstrate that stereocilia consist of a relatively small set of proteins. Most of these, including those involved in transduction and adaptation, are as yet uncharacterized. The availability of purified stereocilia should prove useful in further studies of structure-function relationships in these mechanically sensitive organelles.

Actins↗
PubMed1989

Hypersensitivity pneumonitis in an orchid grower associated with sensitivity to the fungus Cryptostroma corticale.

Hypersensitivity pneumonitis resulting from sensitivity to the fungus Cryptostroma corticale was last reported 20 years ago in association with the occupation of stripping bark from maple logs. A case of hypersensitivity pneumonitis is presented which was associated with exposure to Cryptostroma corticale from non-maple bark chips used to grow orchids. The exposure history and evidence of immune reactivity to the fungus strongly support its causal role in this case.

Alveolitis, Extrinsic Allergic↗
PubMed1987

Logic operations are properties of computer-simulated interactions between excitable dendritic spines.

Neurons in the central nervous system of mammals and many other species receive most of their synaptic inputs in their dendritic branches and spines, but the precise manner in which this information is processed in the dendrites is not understood. In order to gain insight into these mechanisms, simulations of interactions between distal dendritic spines with an excitable membrane have been carried out, using an electrical circuit analysis program for the compartmental representation of a dendrite and several spines. Interactions between responses to single and paired excitatory and inhibitory synaptic inputs have been analyzed. Basic logic operations, including AND gates, OR gates and AND-NOT gates, arise from these interactions. The results suggest the computational power and precision of excitable spines in distal branches of neuronal dendrites, especially those of pyramidal neurons in the cerebral cortex. The applicability to information processing in distal dendrites is discussed.

Computer Simulation↗
PubMed1987

A molecular vocabulary for olfaction.

Olfactory research is entering a new phase, in which molecular mechanisms are being revealed that go considerably beyond traditional concepts. New ways of characterizing these mechanisms are needed, and some suggestions toward that goal have been made in this review. These suggestions recognize that, whereas formerly our terms and concepts regarding olfactory stimulus-response characteristics came mainly from organic chemists and psychophysicists, the main impetus at present comes from molecular biology. A desirable terminology, therefore, is one that is familiar to molecular biologists and can facilitate comparisons with other systems--immune, endocrine, nervous--where similar methods and terms are in use. The suggestions made here for the olfactory system could also be adapted for the taste system. Taste stimulation could be characterized, for example, in terms of gustagens interacting with G-cell receptors, stimulation being determined by the gustatope of a particular ion or molecule. It should be emphasized that such terms and mechanisms may not need to be invoked in studies at behavioral or psychophysical levels. However, the need for them at the receptor level may well be an accurate reflection of our progress in applying methods of molecular biology to these systems.

Odorants↗
PubMed1987

Excitable properties of olfactory receptor neurons.

Action potential-generating properties of olfactory receptor neurons in the olfactory epithelium of the salamander, Ambystoma tigrinum, were studied in control animals, and 2 and 4 weeks after olfactory nerve transection. The threshold for impulse generation in response to injected current was extremely low (74 +/- 46 pA). In addition, the discharge frequencies of the receptor neurons were exquisitely sensitive to small increments of injected current. These high sensitivities may be characteristic of small neurons and stand in contrast to the much lower sensitivities reported for large neurons. The high sensitivity has important implications for the input-output functions of this cell. After nerve transection, both the threshold and the frequency sensitivity decreased. These changes appear to be associated with increased potassium conductance, suggested by prominent membrane rectification and reduced amplitudes of later membrane action potentials in the spike trains. The olfactory receptor neuron appears to be a favorable model for exploring these properties.

Action Potentials↗
PubMed1986

Mapping of an olfactory receptor population that projects to a specific region in the rat olfactory bulb.

An anatomically distinct group of glomeruli, termed the modified glomerular complex (MGC), is present in the posterior dorsomedial portion of the main olfactory bulb. This region has been strongly implicated as part of the pathway that processes odor cues for suckling in neonatal rat pups. We studied the distribution pattern of olfactory receptor neurons that project to the MGC region after ionophoretic injections of WGA-HRP into the olfactory bulbs of 12-day-old rat pups. HRP label was confined to an identifiable localized region in the MGC of the main olfactory bulb. Label extended over 2-7% of the glomerular sheet of the main olfactory bulb, including the MGC. Olfactory receptor neurons within the olfactory epithelium of the nasal cavity were labeled with HRP ipsilateral to the injected side. Maps constructed of the olfactory epithelium revealed that the labeled neurons occurred within topographically defined regions. Anteriorly, labeled olfactory neurons were confined to a narrow strip medial to the dorsal recess, and, more posteriorly, this strip widened medially along the septal wall and laterally onto a limited area on the nasal turbinates. Only a portion of the receptor population within a region was labeled. The boundaries between labeled and unlabeled regions were sharp. These findings support the concept that the olfactory epithelium is an anatomical mosaic in which receptors with different glomerular projections sites are intermingled. In conjunction with previous evidence on the functional specificity of the MGC, and staining of receptor neuron subgroups with monoclonal antibodies, these findings further suggest that olfactory receptor neurons form a functional mosaic within the olfactory epithelium.

Animals↗
PubMed1985

High-resolution 2-deoxyglucose autoradiography in quick-frozen slabs of neonatal rat olfactory bulb.

We have used rapid freezing and freeze-substitution fixation to permit electron microscopic study of [3H]2-deoxyglucose autoradiographs. The techniques minimize diffusion of label into processing fluids and, by inference, migration of label within tissue. Slabs of olfactory bulbs from 12-day-old rats were quick-frozen after one hour of exposure to physiological olfactory stimuli. In light microscopic autoradiographs at low magnification, the neuropil of individual olfactory glomeruli appeared uniformly labeled with different levels of labeling in different glomeruli. At higher magnification, glomerular neuropil labeling consisted of small unlabeled regions surrounded by label clusters, suggesting greater deoxyglucose uptake by olfactory nerve terminals as compared with their postsynaptic dendrites. Periglomerular neurons were labeled differentially. Some microglia and glia precursor cells were heavily labeled in all bulbar laminae. The ultrastructure of cells and neuropil in all bulbar laminae was well-preserved. Cell processes and organelles could be identified in both stained sections and unstained electron microscopic autoradiographs. These experiments demonstrate the feasibility of combining quick-freezing with freeze substitution, in order to extend the resolution of studies using diffusable tracers such as 2-deoxyglucose. The results suggest that this is a promising method for assessing several controversies concerning deoxyglucose incorporation and neuronal and glial metabolism.

Animals↗