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D C Spray

Publications and source records attributed to D C Spray.

At least 181 records · Page 10Linked to original sources
PubMed1984

Developmental uncoupling between blastoderm and yolk cell in the embryo of the teleost Fundulus.

During cleavage and blastula stages of embryos of the teleost Fundulus heteroclitus all of the cells are both electotonically coupled and dye coupled to one another, as determined by microelectrode impalements and spread of Lucifer Yellow. At about the time that gastrulation begins we observed a specific loss of junctional coupling between the yolk cell and cells of the blastoderm. Passage of Lucifer Yellow between the yolk cell and blastoderm was reduced at stage 12 (late blastula), and not detected at stage 13 and thereafter, although cells of the blastoderm remain dye coupled to one another through gastrula stages. Also, junctional electrical coupling between the yolk cell and blastoderm became substantially reduced at stage 13 and thereafter. The loss of coupling at this specific cell apposition and time and the large size of the yolk cell may prove useful in analyzing the underlying cellular mechanisms.

Animals↗
PubMed1984

Gating of gap junction channels.

Gap junctional conductance ( gj ) in various species is gated by voltage and intracellular pH (pHi). In amphibian embryos, gj is reduced to half by a 14 mV transjunctional voltage ( Vj ), a change that in fish embryo requires approximately 28 mV. Crayfish septate axon and pairs of dissociated rat myocytes show no voltage dependence of gj over a range of Vj greater than +/- 50 mV. In fish and amphibian blastomeres , gj is steeply decreased by decrease in pHi (n, Hill coefficient: 4.5) and the apparent pKH (7.3) is in the physiological range. In crayfish septate axon the pKH is lower (6.7) and the curve is less steep (n = 2.7). Rises in cytoplasmic Ca can also decrease gj but much higher concentrations are required (greater than 0.1 mM in fish blastomeres). Voltage and pH gates on gap junctions in amphibian embryos appear independent. In squid blastomeres pH gates exhibit some sensitivity to potential, both transjunctional and between inside and outside. A pharmacology of gap junctions is being developed: certain agents block gj directly (aldehydes, alcohols, NEM in crayfish); others block by decreasing pHi (esters that are hydrolyzed by intrinsic esterases, NEM in vertebrates, and, as in the experiments demonstrating the effect of pHi, weak acids). Certain agents block pH sensitivity without affecting voltage dependence (retinoic acid, glutaraldehyde, EEDQ), further indicating separateness of pH and voltage gates. These studies demonstrate a dynamics of gap junctional conductance and variability in gating in a series of possibly homologous membrane channels.

Amphibians↗
PubMed1984

Determination of synaptic phenotype: insulin and cAMP independently initiate development of electrotonic coupling between cultured sympathetic neurons.

Electrotonic coupling between pairs of sympathetic neurons dissociated from superior cervical ganglia of neonatal rats is rare when cells are cultured for 2 weeks in a nutrient medium plus serum and is common when cells are cultured for the same period in serum-free defined medium. This defined medium is the same nutrient medium with five added factors (progesterone, transferrin, putrescine, insulin, and selenium). When added singly to serum-containing medium, insulin and, to a lesser extent, selenium promote the development of electrotonic and dye coupling. The insulin effect is obtained with doses as low as 0.01 microgram/ml and is maximal after exposures from 3 to 5 days. The incidence of electrotonic coupling is also enhanced by exposure of cells to dibutyryl cAMP. This effect is obtained with doses as low as 0.1 mM, is faster (being maximal at approximately equal to 12 hr exposure), and is prolonged in the presence of the phosphodiesterase inhibitor caffeine. Butyrate itself promotes coupling to a small extent, but cAMP involvement is confirmed by similar effects of other membrane permeant analogues. Endogenous levels of cAMP are significantly elevated in cultures grown in the defined medium but not in those in serum-containing medium to which insulin or selenium are added. We conclude that the promotion of coupling by cAMP and by insulin or selenium are independent. The development of coupling in the defined medium thus seems to be a consequence of the addition of promoting substances (insulin, selenium) and the removal of an inhibitory effect of serum on cAMP levels.

Animals↗
PubMed1984

Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification.

Conductance of gap junctions in many preparations has been shown to be sensitive to cytoplasmic pH, decreasing as pH decreases below 7.5 in fish and amphibian embryos and below 7.1 in crayfish septate axon. We have found a new class of compounds, benzyl acetate derivatives, that reversibly decrease junctional conductance, gj, when applied in low concentration (approximately 1 mM). Simultaneous intracellular pH (pHi) measurements show that the ester effects are attributable to reduction in pHi. The sensitivity of gj to these compounds and the relative lack of side effects make these agents attractive for studies of the role played by gap junctions in normal tissue function. In addition, the finding of cytoplasmic acidification in response to cell exposure to esters suggests caution in interpretation of results obtained using esterified compounds for intracellular loading.

Animals↗
PubMed1983

Gap junctions and septate-like junctions between neurons of the opisthobranch mollusc Navanax inermis.

The buccal ganglia of Navanax inermis were studied by thin section, lanthanum infiltration and freeze fracture. Freeze fracture clearly demonstrates small gap junctions between neuronal processes in the neuropil, many of which are known to be electrotonically coupled. Junctional particles cleave with the P-face. In thin section, gap junctions appeared as small blurred contacts, presumably because of the small size of the junctions. Lanthanum infiltration was poor and failed to aid in identifying gap junctions. However, it did reveal septate-like junctions whose septa were not osmiophilic. Corresponding E-face grooves and ridges were seen in freeze fracture, sometimes adjacent to gap junctions. The septate-like junctions have parallel membranes and may have been mistaken for gap junctions in several other thin section studies of invertebrate neurons.

Animals↗
PubMed1983

Control of intercellular communication by voltage dependence of gap junctional conductance.

The junctional conductance between coupled amphibian blastomeres exhibits a high degree of voltage dependence, as previously described in voltage clamp studies (Spray, D.C., A.L. Harris, and M.V.L. Bennett (1981) J. Gen. Physiol. 77: 77-95; Harris, A.L., D.C. Spray, and M.V.L. Bennett (1981) J. Gen. Physiol. 77: 95-117). The present study examines the properties which this voltage dependence confers on electrotonic coupling between cells. The effects of applied pulses and ramps of current are studied experimentally and are modeled by calculation. During sufficiently large current pulses applied to one cell of a pair, the cells uncouple and then recouple after termination of the pulses. Ramps of current applied to one of the cells can give voltage-current (V-I) relations with a region of hysteresis within which the cells are stably coupled or stably uncoupled depending on previous history. Intrinsically generated currents are able to cause bistability of coupling in the absence of externally applied current. Calculations from the parameters of junctional conductance defined under voltage clamp fully account for these findings and illustrate how junctional and nonjunctional conductances affect the V-I relations in the region of bistability. Recordings from several cells within a small group show that boundaries of intercellular communication can be altered by applied current, a finding that also can be accounted for by voltage dependence of junctional conductance. The "Appendix" examines quantitatively the criteria required for bistability of coupling and the relevance of bistability for intercellular signaling. The plasticity of coupling which the voltage dependence of junctional conductance confers on cells offers an intriguing mechanism by which patterns of intercellular communication could be determined and changed in developing tissues.

Ambystoma↗
PubMed1982

Gap junctional conductance: comparison of sensitivities to H and Ca ions.

One cytoplasmic aspect of the junctional membrane between coupled pairs of Fundulus blastomeres was perfused with solutions of known H and Ca ion concentrations. Conductance of junctional membrane was decreased by either ion. The sensitivity to H ions was about 10,000 times greater than that to Ca ions. The results suggest that junctional conductance can be modulated by changes in H ion concentration near physiological pH, but that unphysiologically high concentrations of Ca ion, such as would be reached only on cell death, are required for comparable changes in junctional conductance.

Animals↗
PubMed1981

Gap junctional conductance is a simple and sensitive function of intracellular pH.

The pH of the cytoplasm (pHt) measured with pH-sensitive microelectrodes in cleavage-stage blastomeres of amphibian (Ambystoma) and teleost (Fundulus) embryos is about 7.7. In electrotonically coupled cell pairs, junctional conductance is rapidly and reversibly reduced by acidification of the cytoplasm. The relation between junctional conductance and pHi is the same for increasing and decreasing pH and is independent of the rate of change over a wide range. The relation is well fitted by a Hill curve with K = 50 nM (pK = 7.3) and n = 4 to 5. The closure of gap junction channels at low pHi appears to be a cooperative process involving several charged sites. The absence of hysteresis and identity of effects for fast and slow pHi changes implies that protons act directly on the channel macromolecules and not through an intermediate in the cytoplasm.

Ambystoma↗
PubMed1981

Equilibrium properties of a voltage-dependent junctional conductance.

The conductance of junctions between amphibian blastomeres is strongly voltage dependent. Isolated pairs of blastomeres from embryos of Ambystoma mexicanum, Xenopus laevis, and Rana pipiens were voltage clamped, and junctional current was measured during transjunctional voltage steps. The steady-state junctional conductance decreases as a steep function of transjunctional voltage of either polarity. A voltage-insensitive conductance less than 5% of the maximum remains at large transjunctional voltages. Equal transjunctional voltages of opposite polarities produce equal conductance changes. The conductance is half maximal at a transjunctional voltage of approximately 15 mV. The junctional conductance is insensitive to the potential between the inside and outside of the cells. The changes in steady-state junctional conductance may be accurately modeled for voltages of each polarity as arising from a reversible two-state system in which voltage linearly affects the energy difference between states. The voltage sensitivity can be accounted for by the movement of about six electron charges through the transjunctional voltage. The changes in junctional conductance are not consistent with a current-controlled or ionic accumulation mechanism. We propose that the intramembrane particles that comprise gap junctions in early amphibian embryos are voltage-sensitive channels.

Ambystoma mexicanum↗
PubMed1981

Kinetic properties of a voltage-dependent junctional conductance.

We have proposed that the gap junctions between amphibian blastomeres are comprised of voltage-sensitive channels. The kinetic properties of the junctional conductance are here studied under voltage clamp. When the transjunctional voltage is stepped to a new voltage of the same polarity, the junctional conductance changes as a single exponential to a steady-state level. The time constant of the conductance change is determined by the existing transjunctional voltage and is independent of the previous voltage. For each voltage polarity, the relations between voltage, time constant, and steady-state conductance are well modeled by a reversible two-state reaction scheme in which the calculated rate constants for the transitions between the states are exponential functions of voltage. The calculated rate constant for the transition to the low-conductance state is approximately twice as voltage dependent as that for the transition to the high-conductance state. When the transjunctional voltage polarity is reversed, the junctional conductance undergoes a transient recovery. The polarity reversal data are well modeled by a reaction scheme in which the junctional channel has two gates, each with opposite voltage sensitivity, and in which an open gate may close only if the gate in series with it is open. A simple explanation for this contingent gating is a mechanism in which each gate senses only the local voltage drop within the channel.

Ambystoma mexicanum↗
PubMed1980

Synaptic organization of expansion motoneurons of Navanax inermis.

The opisthobranch mollusc, Navanax, feeds by rapid pharyngeal expansion that sucks in prey followed by peristaltic swallowing that moves prey into the esophagus. Several identifiable neurons on the ventral surface of the buccal ganglia control radial musculature within the pharyngeal wall, contraction of which leads to pharyngeal expansion. These are considered expansion motoneurons because their axons run into the muscle and twitches and EMGs occur one for one with action potentials. The motoneurons are electrotonically coupled. Electrotonic PSPs, the components of spread associated with impulses, can summate with subthreshold DC depolarizations to yield synchronous impulses in coupled cells. During a train of responses the later electrotonic PSPs can be facilitated because of increase in amplitude and duration of the presynaptic impulses. Expansion motoneurons are synaptically connected by two apparently interneuronal pathways: a low threshold pathway activated by subthreshold depolarization of the two largest expansion motoneurons (the G-cells) that inhibits the entire population, and a high threshold pathway that is activated by a train of G-cell impulses and produces largely excitatory PSPs in the smaller expansion motoneurons and an EPSP--IPSP sequence in the G-cells. Coupling among expansion motoneurons can be abolished by chemical inhibitory synaptic inputs that are activated by electrical stimulation of the pharyngeal nerve or tactile stimulation of the pharyngeal wall. This uncoupling phenomenon can be explained by a simple equivalent circuit in which inhibitory synapses along the coupling pathway short circuit electrotonic spread. Uncoupling can outlast the evoking stimulus by several seconds. During uncoupling the smaller expansion motoneurones can fire independently while the G-cell is inhibited, and impulses still propagate from somata to the periphery. The expansion motoneuron population receives excitatory input from the mechanoreceptors in protractor muscles. Mechanical stimulation of the pharyngeal wall activates primary sensory neurons in the buccal ganglia that fire during excitation and during inhibition and uncoupling of expansion motoneurons.

Animals↗
PubMed1980

Peripheral fields and branching patterns of buccal mechanosensory neurons in the opisthobranch mollusc, Navanax inermis.

A population of about 75 primary sensory cells were identified on the dorsal surface of each buccal ganglion of Navanax. Each sensory cell possesses at least one mechanosensitive field in the pharyngeal wall or lips that correlates somatotopically with its position in the buccal ganglia. Many cells had additional fields that could be widely separated, requiring that their afferent processes branch. Cells were found with processes in more than one buccal nerve and with multiple processes in the same nerve. Hyperpolarization of the soma or repetitive electrical or physiological stimulation could cause failure of centripetal propagation of impulses. Impulses initiated in different branches could fail at different distances from the soma. Axon spikes that fail to invade the soma may or may not invade other branches. Axon spikes in separate branches that fail to invade the soma can summate to initiate an invading impulse. These findings suggest that integration of information from different branches may occur in a single sensory neuron.

Animals↗
PubMed1980

Synaptic connections of buccal mechanosensory neurons in the opisthobranch mollusc, Navanax inermis.

Mechanical stimulation of various areas of the pharyngeal wall and lips can produce EPSPs and IPSPs, as well as abruptly rising impulses, in primary sensory cells. IPSP fields are generally larger than EPSP fields and these fields are distributed without obvious order around fields from which afferent spikes are evoked. Apparently monosynaptic excitatory and inhibitory contacts are formed between primary sensory neurons. These synapses are blocked by high Mg2+ indicating chemical transmission. IPSPs are inverted by Cl- injection. Excitatory inputs can be electrically far from the soma. Sensory cells form apparently monosynsptic excitatory or inhibitory contacts on motoneurons mediating pharyngeal expansion. Brief sensory excitation can initiate sustained firing within this neuronal population and sustained synaptic activity in motoneurons. Interactions of sensory neurons may be important in information processing and in generating motor paterns. These neurons serve both primary sensory and interneuronal functions.

Animals↗
PubMed1980

Gap junctions in early amphibian embryos.

Cell pairs from late cleavage and early blastula Ambystoma mexicanum embryos were found to be electrotonically coupled. Thin-section electron microscopy revealed typical gap junctions between the cells. Freeze-fracture electron microscopy showed the gap junctions to be comprised of aggregations of 8.5-nm P-face particles and corresponding E-face pits. The conductance of the amphibian embryonic gap junction is known to be voltage-dependent, but no obvious gating structure was resolved by these morphological techniques.

Ambystoma mexicanum↗
PubMed1979

Voltage dependence of junctional conductance in early amphibian embryos.

Isolated pairs of blastomeres from early amphibian embryos (Ambystoma, Rana, Xenopus) are electrontonically coupled. Junctional conductance and permeability to the dye Lucifer Yellow are markeldy and reversibly decreased by moderate transjunctional polarization in either direction. The relationship between junctional conductance and transjunctional voltage is sufficiently steep that a physiological role in regulation of intercellular communication is plausible.

Ambystoma↗
PubMed1976

Electrotonic coupling: effective sign reversal by inhibitory neurons.

Neurons in the buccal ganglia of Navanax inermis which control circumferential muscles of the pharynx showed typical electrotonic coupling when there was little synaptic activity in them. When there was much inhibitory activity, the effective sign of coupling was reversed; that is, hyperpolarization and depolarization of one cell caused depolarization and hyperpolarization of the others. A neural circuit explaining these results involes inhibitory neurons electronically coupled to and also inhibitory to the circumferential neurons that are themselves coupled. This circuit offers considerable flexibility for mediation of different activity patterns in this simple neuronal system.

Action Potentials↗