Swelling of the Transverse Tubular System in Frog Sartorius

Electron microscopy shows that the transverse tubular system of frog sartorius swells in Ringer fluid in which NaCl is partially replaced by sucrose (sucrose isotonic solutions). At constant tonicity, the degree of swelling is roughly proportional to the decrease in ionic strength and to the sucrose concentration of the bathing solution. Swelling is time-dependent and reversible within 2 hr. The late after potential which follows a train of impulses is prolonged with swelling, but not to the extent expected from the model of Adrian and Freygang. This discrepancy remains unexplained, as does the mechanism of swelling of the transverse tubular system, although some suggestions are offered. One is that the transverse tubular system contains fixed charges and swells like a fixed charge gel.     

Observations on “Detubulated” Muscle Fibres

GLYCEROL treatment of striated muscle^1–3 has been widely assumed to be a means of disconnecting the transverse tubular system from the surface membrane. Exposure of a sartorius muscle to Ringer plus 400 mM glycerol followed by a return to Ringer, reduces the membrane capacity of superficial fibres and the muscle is mechanically inactive even though the fibres can transmit action potentials; both these effects might be expected if the transverse tubular system was destroyed or disconnected from the extracellular fluid. We have studied this mechanical decoupling on isolated muscle fibres from the semitendinosus, examining the effects of glycerol concentration. Our results suggest that decoupling may be a complex process and in particular they show that under some circumstances both the depolarization and the loss of the twitch can be reversed by re-exposure to glycerol.     

Mass Transfer in the Cornea: II. Ion Transport and Electrical Properties of a Series Membrane Tissue

The electrical and active transport properties of isolated rabbit cornea are investigated by computer experimentation. The tissue is modeled as a series membrane system and the passive ion fluxes through it are described by the frictional formulation of irreversible thermodynamics. From short-circuit current (SCC) data, it is found that the epithelial sodium pump rate (P) is not appreciably changed when much of the sodium in the solution bathing the anterior corneal surface (concentration = c₁₁) is replaced by choline, with choline-free medium posteriorly. Simulations of open-circuited corneas, using the mean P computed from the SCC data, yield corneal and stromal potentials in agreement with experiment. The stromal fluid is calculated to become more hypotonic as c₁₁ is diminished, a result consistent with posttest measurements of the sodium content of experimental stromata. The apparent decrease in “bound sodium” which accompanies the reduction of c₁₁ is a result of the associated changes in steady stromal hydration; the epithelial sodium pump does not contribute to corneal deturgescence. The inclusion of a simple epithelial structure in the computations changes the value of P but affects neither its constancy nor the calculated behavior of the cornea under open-circuit conditions. A general algebraic relation among pump rates and ion fluxes in short-circuited series membrane systems bathed in complex media is derived and used to construct a relation between P and SCC for the cornea. This equation yields pump rates in good agreement with the computer results and is used to show that (a) P is independent of c₁₁ if d(SCC)/dc₁₁ is a constant related to the over-all corneal permeability to sodium, and (b) a Lineweaver-Burke plot of 1/SCC vs. 1/c₁₁ can appear to be linear at constant P.     

REVIVAL OF MAMMALIAN SPERM AFTER IMMERSION IN LIQUID NITROGEN

1. A wide variety of procedures was used to test the motility of mammalian sperm after plunging them into liquid nitrogen at –195°C. and later rapidly warming them to 35°C. by plunging them into a suitable balanced and isotonic medium. 2. Using seminal fluid sperm from the same human donor, maximal numbers of motile sperm survived vitrification when the samples were (a) very fresh, (b) untreated with plasmolysing solutions, (c) plunged into the refrigerant in the form of a foam. The maximum yield of motile human sperm recoverable from the liquid nitrogen was 50 per cent. Since in this sample only 75 per cent of the sperm were alive before immersion, 67 per cent of the living sperm survived vitrification. 3. Experiments with sperm from 31 rabbits were made with a variety of conditions of pretreatment to obtain maximal yields of recoverable, motile sperm after vitrification by liquid nitrogen. (a) A consistent recoverable yield of about 0.5 per cent was obtained when the untreated suspension of sperm was smeared on cellophane and partially dried in air before immersing in liquid nitrogen. (b) On a few out of many occasions plasmolysis for several minutes with hypertonic Ringer solution gave a recoverable yield of 0.1 per cent as did (c) pretreatment with hypertonic Ringer and butyric acid.     

Effect of charge changes in ligand-triggered membrane cooperative transitions

An analysis is given for the influence of surface charge changes due to ligand-receptor interactions in the membrane cooperative transitions. The simple case of two allosteric states accessible each to one ligand is considered using affinity constant earlier described in terms of surface properties. It is found that if indeed there are membrane cooperative effects, some decrease in charge facilitates the appearance of very “sharp” first-order transitions, even supposing that cooperativity parameter values are far above the normally critical value Λ_c = e^?4. When the charge is increased, however, phase transitions are delayed and only assume a threshold response if Λ < e^?4. It is concluded that such contact-dependent effects might be implicated in membrane control action for cell proliferation.     

Isolation and some properties of extracellular d-glucosyltransferases and d-fructosyltransferases from Streptococcus mutans serotypes c, e, and f

Extracellular d-glucosyltransferases (GTase) and d-fructosyltransferases (FTase) were isolated from Streptococcus mutans IB (serotype c), B14 (e), and OMZ175 (f) by chromatofocusing, followed by hydroxyapatite column chromatography. The GTases isolated from serotypes c, e, and f are basic proteins (pI 7.4). The serotype c and e enzymes have two protein components having M_r 173 000 and 158 000 and the enzyme of the serotype f one component having M_r 156 000. The GTases of all the serotypes showed a K_m value for sucrose of 10–14mm and an optimum pH 5.5–6.0 for enzyme activity, and their activities were enhanced by the presence of primer Dextran T10. The α-d-glucans synthesized by the purified GTases are water soluble and primarily consist of (1→6)-α-d-glucosidic linkage (41–66 mol/100 mol) and α-d-(1→3,6)-branch linkage (6–20 mol/100 mol), but significant proportions of α-d-(1→3), α-d-(1→4), and α-d-(1→3,4) linkages (11, 6, and 14 mol/100 mol, respectively) were detected in the serotype c α-d-glucan. The isolated FTases of the serotypes c, e, and f are acidic enzymes (pI 4.6) and consist of two components having M_r 84 000 and 76 000 for the serotype c enzyme, and 106 000 and 84 000 for the serotypes e and f enzymes, respectively. The K_m value for sucrose was 6, 10, and 17mm for the serotypes c, e, and f enzymes, respectively, and the optimum pH of enzymic activity 5.5–6.0. Reactivity with Concanavalin A, susceptibility to acid hydrolysis, and paper chromatography of the hydrolyzates suggested that the water-soluble β-d-fructans synthesized by the purified FTases were of the inulin-type and had chemical structures somewhat different among the serotypes.     

Kinetic analysis of bacterial reaction centers reconstituted in lipid bilayers

(1) Reaction center-lipid complexes were extracted into octane solutions. Different methods for generating an assymetric membrane distribution of reaction centers are discussed, which allow the measurement of electrical signals upon illumination. (2) The dichroism of the chromophoric groups in the reaction centers was investigated in planar lipid bilayers and the angle β between each transition moment and the normal to the membrane could be determined to be β(757 nm) = 29.5 ± 1.2, β(801 nm) = 34 ± 1.0 and β(860 nm) = 41.3 ± 0.9°. (3) The kinetics of the reaction centers from Rhodopseudomonas sphaeroides were analysed by electrical measurements and the relevant rate constants could be determined. In addition, the interaction between reaction centers and the intramembrane, ubiquinone-containing pool was investigated and described in a kinetic model. (4) The interaction between the electron-donating ferrocytochromes exhibited two distinguishable sources, a fast accessible, membrane-bound pool, which is limited by diffusion, and a pool consisting of an aqueous solution of ferrocytochrome c, which is accessible with a slower rate constant.     

Large Scale Global Structural Changes of the Purple Membrane during the Photocycle

Both the solution and the oriented film absorption and circular dichroic spectra of the bacteriorhodopsin (bR₅₆₈) and M₄₁₂ intermediate of the purple membrane photocycle were compared over the wavelength region 800-183 nm to assess structural changes during this photocycle. The main findings are (a) loss of the excitonic interaction among the chromophoric retinal transitions indicating disordering of the retinal orientations in the membrane and distortions of the membrane hexagonal crystal lattice, (b) structural change of the chromophoric retinal, (c) changes in the key interactions between the retinal and specific groups in the local environment of the apoprotein, (d) significant changes of the tertiary structure of the bR with negligible secondary structure involvement, and (e) a net tilting of the rodlike segments of the bR polypeptides away from the membrane normal. These findings are in accord with large scale global structural changes of the membrane during the photocycle and with structural metastability of the bR molecules. An important implication of these changes is the possibility of transmembrane retinal-regulated pulsating channels during the photocycle. The significance of this possibility in respect to models for the proton translocation function of this membrane is discussed.     

Water Transfer and Cell Structure in Isolated Crayfish Muscle Fibers

Changes in volume of crayfish single muscle fibers in response to changes in ionic or electrical conditions have been studied in conjunction with electrophysiological measurements and electron microscopic examinations. The occurrence of at least three mechanisms of water movements is revealed, two being processes which are superimposed on the normal osmotic water movement that results from a change in the concentration of solute in the medium. Differences between the time courses of the changes in volume and potential on changing K_i/K_o indicate that water may be distributed unequally for a time within compartments of the fiber. Electron micrographs reveal a selective accumulation of water at the periphery of the fiber under certain conditions. A correlation of H₂O transfer with a change in membrane potential is apparent in crayfish muscle fibers and is probably due to electroosmotic effects. Electrokinetic water movements are produced whenever the membrane potential is changed to a considerable degree by changing the level of K and/or Cl in the medium, or by applying currents with an intracellular microelectrode. Depolarizations cause shrinkage. Hyperpolarizations or repolarizations cause swelling. The volume changes are independent of the occurrence or absence of swelling in the anion-permselective transverse tubular system. They indicate that the fiber membrane along the surface is heterogeneous, not only with respect to the signs of its fixed charge sites, but also with respect to the sizes and relative permselectivities of these charged channels.     

Localization and concentration of hydroxylamine oxidoreductase and cytochromes c-552, c-554, cm-553, cm-552 and a in Nitrosomonas europaea

Two membrane-associated cytochromes, cytochrome c_m-553 and cytochrome c_m-552, were derived from Nitrosomonas europaea. The major c-type cytochrome, cytochrome c_m-553, accounted for 92% of the c heme found in the membrane. It had absorption maxima at 410 nm in the oxidized form and at 417, 523 and 553 nm in the dithionite reduced form. Cytochrome c_m-552 possessed absorption maxima at 409 nm in the oxidized form, at 421, 522 and 552 in the dithionite reduced form, and at 418 in the dithionite reduced plus CO form. The concentration and cellular distribution of the two c-type membrane cytochromes, hydroxylamine oxidoreductase and cytochromes c-552, c-554, and a were determined. Over 95% of the soluble cytochromes (hydroxylamine oxidoreductase cytochromes and c-552 and c-554) were periplasmic, whereas cytochrome c_m-553, cytochrome c_m-552 and cytochrome a were associated with the cell membrane. The outer membrane and cytoplasm were devoid of cytochromes. The extracytoplasmic location of the proton-yielding hydroxylamine oxidizing system (NH₂OH ™ HNO + 2H⁺ + 2e⁻) may contribute to an energy-linked proton gradient. The heme concentrations of hydroxylamine oxidoreductase and cytochromes c-552, c-554, c_m-553, c_m-552 and a were approx. 2.4, 1.2, 0.3, 1.3, 0.1 and 1.1 nmol/mg cell protein, respectively. The corresponding molar ratios of heme were 22:11:2.9:12:1.0:10. The enzyme or cytochrome concentrations for hydroxylamine oxidoreductase and cytochromes c-552, c-554, c_m-553, c_m-552 and a were approx. 0.13, 1.05, 0.09, 0.63, 0.055 and 0.56 nmol/mg cell protein, respectively. The corresponding molar ratios were 0.24:2.2:0.16:1.2:0.1:1.0.     

On the Inhibition of Muscle Contraction Caused by Exposure to Hypertonic Solutions

The evidence supporting a site of inhibition of excitation contraction (E-C) coupling near the plasma membrane (the "glycerol effect," the K⁺-potentiating effect) for muscle in hypertonic solution was reinvestigated. It was found, using whole frog sartorii, that there was a rehydration of muscle soaked in glycerol Ringer after 30 min and a large swelling (to 140% after 1 hr soaking) upon return of the muscle to normal Ringer, suggesting that significant amounts of glycerol enter the fibers during this time. While contrary to the original report of the glycerol effect, this finding was consistent with other studies involving the use of single fibers. Also reexamined was the potentiating effect of K⁺ on the hypertonic inhibition of muscle contraction. It was found that muscles exposed to this KCl pretreatment swell so that they are less dehydrated in hypertonic solutions, thus accounting for the observed potentiation. After being treated instead with a K₂-tartrate Ringer solution, muscles did not swell and, as determined with twitch recordings, did not display any potentiation in hypertonic solutions—even though the [K₊] was higher than an osmotically equivalent KCl solution. The evidence was thus consistent with alternative hypotheses in which inhibition of contraction occurs at a later stage in E-C coupling or involves the contractile process itself.     

The Potential Distribution and the Short-Circuiting Factor in the Sucrose Gap

The sucrose gap technique, though widely employed in many tissues, could not be used for quantitative measurements of the membrane potential, because the value of the short-circuiting factor and the influence of junction potential on the recorded potential difference were unknown. The formula that relates the recorded potential to the true resting membrane potential was found by application of the cable equations to a core conductor placed in a system with three different media, e.g. Ringer, sucrose, and KCl. The formula shows that the potential difference recorded over the sucrose insulator depends on the extracellular and the intracellular longitudinal resistances, the membrane resistance and the membrane potentials in each region, and on the junction potentials between the different media. The true membrane potential in the Ringer region can be calculated from the potential difference recorded after complete depolarization by KCl on one side of the preparation, if the longitudinal resistances, the membrane resistances, the extracellular potential in the sucrose, and the junction potential between Ringer and sucrose are determined by separate measurements.     

Changes in the Membrane Permeability of Frog's Sartorius Muscle Fibers in Ca-Free EDTA Solution

The changes in the membrane permeability to sodium, potassium, and chloride ions as well as the changes in the intracellular concentration of these ions were studied on frog sartorius muscles in Ca-free EDTA solution. It was found that the rate constants for potassium and chloride efflux became almost constant within 10 minutes in the absence of external calcium ions, that for potassium increasing to 1.5 to 2 times normal and that for chloride decreasing about one-half. The sodium influx in Ca-free EDTA solution, between 30 and 40 minutes, was about 4 times that in Ringer's solution. The intracellular sodium and potassium contents did not change appreciably but the intracellular chloride content had increased to about 4 times normal after 40 minutes. By applying the constant field theory to these results, it was concluded that (a) P_Cl did not change appreciably whereas P_K decreased to a level that, in the interval between 10 and 40 minutes, was about one-half normal, (b) P_Na increased until between 30 and 40 minutes it was about 8 times normal. The low value of the membrane potential between 30 and 40 minutes was explained in terms of the changes in the membrane permeability and the intracellular ion concentrations. The mechanism for membrane depolarization in this solution was briefly discussed.     

Pressure-volume relationship of the Fundulus egg in sea water and in sucrose

Upon activation, an internal hydrostatic pressure develops within the Fundulus egg, and compresses the egg proper to a reduced volume. When the perivitelline pressure is abolished by a highly hypertonic sucrose solution, the egg volume increases. As sucrose penetrates the chorion, the volume again decreases. The relation between P and V in these conditions is inverse, and approximates a rectangular hyperbola. The limiting factor causing most of the deviation is shown to be the incompressible fraction. It is concluded that the volume of the egg proper is controlled by the perivitelline pressure, and that the effect of hypertonic sucrose solution is exerted by lowering the pressure and thereby increasing membrane permeability non-specifically. It is also shown that some permanent alterations occur within the plasma membrane during activation that reduce the permeance, and thereby, increase the incompressible fraction.     

Effective population sizes in cattle,sheep, horses,pigs and goats estimated from census and herdbook data

Accurate measures of effective population sizes (N_e) in livestock require good quality data and specialized skills for their computation and analysis. N_e can be estimated by Wright’s equation N_e=4MF/(M+ F) (M, F being sires and dams, respectively), but this requires assumptions which are often not met. Total census sizes N_c of livestock breeds are collated globally. This paper investigates whether estimates of N_e can be made from N_c; this would facilitate conservation monitoring. Some N_e methodologies avoid the assumptions of Wright’s equation and permit measurement, rather than estimation, of N_e. Those considered here employ, respectively, linkage disequilibrium (LD) of single-nucleotide polymorphisms (yielding N_e(LD)), and genealogical analysis (rate of increase of inbreeding, DF), yielding N_e(DF). Considering breeds of cattle, sheep, horses, pigs and goats for which N_c and either N_e(LD) or N_e(DF) are known (totals of 203 breeds and 321 breeds, respectively), proportionality has been investigated between N_c and these measures of N_e. N_e(LD) was found to increase with N_c, significantly in sheep and horses, less so in cattle, but not at all in pigs. N_e(DF) was correlated with log₁₀(N_c) in cattle, sheep and horses (53, 56, 43 breeds, respectively). N_e(LD) was correlated in cattle (73 breeds) and pigs (31 breeds) with the log₁₀ transformation of N_e as calculated by Wright’s equation. Further verification and refinement are needed, particularly of census data, but credible predictions of N_e are obtainable by applying the following multipliers to log₁₀(N_c): cattle 17.61, sheep 97.72, horse 70.78. For cattle and pigs, multiplying log₁₀(N_e(Wright)) by, respectively, 40.69 and 60.09, also gives credible predictions. Such census-based estimates of N_e could in principle be generated by non-specialists and are likely to be suited to audits of conservation activity when financial resources or availability of data are limiting. The ratio N_e/N_c varied among species with an overall median value of 0.03, less than a tenth of that typically observed in wild mammals. Characteristics were also investigated of a distinct herdbook-based methodology, namely the development of Wright’s equation to take into account variances of progeny numbers to yield what has been termed here N_e (Hill). Comparison of these values with N_e (Wright) could help to identify breeds with breeding structures conducive or inimical to genetic conservation. However, N_e(Hill) requires breed-specific values for these variances, and this restricts its applicability.     

Changing electrical constants of the Fundulus egg plasma membrane

Electrical constants of the plasma membrane of the Fundulus egg have been measured with microelectrodes by the transient method. No consistent and significant membrane potential was measured. Membrane capacity averages 0.63 µF/cm.² for both unactivated and activated eggs. Membrane resistance averages 3450 ohm-cm.² in the unactivated eggs, but increases 2 to 7 times to an average of 13,290 ohm-cm.² in the fully activated state. In a hypertonic sucrose solution, the swelling of the egg proper is accompanied by a rapid fall of membrane resistance towards that in the unactivated state. The changes of the membrane resistance are interpreted as probably caused by alterations in the effective pore size in the plasma membrane.     

Electrogenicity, pH-Dependence, and Stoichiometry of the Proton-Sucrose Symport

The electrogenicity, pH-dependence, and stoichiometry of the proton-sucrose symport were examined in plasma membrane vesicles isolated from sugar beet (Beta vulgaris L. cv Great Western) leaves. Symport mediated sucrose transport was electrogenic as demonstrated by the effect of membrane potential on ΔpH-dependent flux. In the absence of significant charge compensation, a low rate of sucrose transport was observed. When membrane potential was clamped at zero with symmetric potassium concentrations and valinomycin, the rate of sucrose flux was stimulated fourfold. In the presence of a negative membrane potential, transport increased six-fold. These results are consistent with electrogenic sucrose transport which results in a net flux of positive charge into the vesicles. The effect of membrane potential on the kinetics of sucrose transport was on V_max only with no apparent change in K_m. Sucrose transport rates driven by membrane potential only, i.e. in the absence of ΔpH, were comparable to ΔpH-driven flux. Both membrane potential and ΔpH-driven sucrose transport were used to examine proton binding to the symport and the apparent K_m for H⁺ was 0.7 micromolar. The kinetics of sucrose transport as a function of proton concentration exhibited a simple hyperbolic relationship. This observation is consistent with kinetic models of ion-cotransport systems when the stoichiometry of the system, ion:substrate, is 1:1. Quantitative measurements of proton and sucrose fluxes through the symport support a 1:1 stoichiometry. The biochemical details of protoncoupled sucrose transport reported here provide further evidence in support of the chemiosmotic hypothesis of nutrient transport across the plant cell plasma membrane.     

The Relation Between the Late After-Potential and the Size of the Transverse Tubular System of Frog Muscle

This is an investigation of the effects on the late after-potential of immersing frog sartorius muscles in three kinds of modified Ringer's fluid; hypertonic, low chloride, and potassium-free. The late after-potential has been attributed to the depolarizing effect of an accumulation of potassium, during a preceding train of impulses, in the intermediary space of the model of a muscle fiber proposed by Adrian and Freygang. Both the hypertonic and low chloride solutions prolonged the late after-potential reversibly and the potassium-free solution shortened it. The effect of the low potassium solution fitted those data calculated from the model, but the effect of the hypertonic and low chloride solutions required an increase in size of the intermediary space of the model in order to fit the calculated data. An electron microscopic study of the muscles showed that the size of the transverse tubular system changed reversibly in the hypertonic and low chloride solutions in almost the amount necessary to fit the experimental data to the calculated data. This agreement between the change in size of the transverse tubular system and that of the intermediary space indicates that the intermediary space may be the transverse tubular system.     

Alterations of ultrastructure and physiology of chemoreceptor dendrites in blowfly taste hairs treated with vinblastine and colchicine

Vinblastine (10^?3 M) and colchicine (10^?2 M) dissolved in fly Ringer solution were applied to chemoreceptor dendrites in individual tarsal taste hairs of blowflies (Phaenicia serricata Meigen), and the resultant changes in the morphology and physiological responsiveness of the receptors were examined. While Ringer solution alone did not have any morphological or physiological effects, treatment with drugs dissolved in Ringer solution increased the latency of responses to sucrose and NaCl and decreased spike amplitude and frequency. The drugs also disrupted microtubules and caused the destruction of the distal end of the dendrites. The observations provide evidence that the microtubules have a role in maintaining the structural integrity of the dendrites. Anodal current applied along with a chemical stimulus (NaCl or sucrose) increased the action potential frequency of treated and untreated receptors, and the electrical current elicited spikes only from those receptors which were activated by the chemical stimulus alone. When drug treatment resulted in a complete cessation of response to chemical stimuli, the receptors were also unresponsive to electrical stimulation. The results of this study are discussed in relation to hypotheses of transduction in chemoreception.     

Metabolism of excised rat skin in hypertonic media

The rate of oxygen consumption by rat skin is inhibited similarly by hypertonic solutions of NaCl, KCl, and sucrose. The rate of anaerobic glycolysis is inhibited by hypertonic NaCl. The inhibition of QO₂ by NaCl concentrations above about 2 osmols per liter is not reversible.