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J Pernberg

Publications and source records attributed to J Pernberg.

7 recordsLinked to original sources

Comparison of the selectivity of postsynaptic potentials and spike responses in cat visual cortex.

Intracellular recordings were made from neurons in the cat visual cortex (area 17) to compare the orientation and direction selectivities of the output of a cell with those of the input the cell receives. The input to a cell was estimated from the PSPs (postsynaptic potentials) evoked by visual stimulation, and the output estimated from the number of spikes generated during the same responses. For the whole sample, selectivity of the output of cells was significantly higher than selectivity of their input. Upon PSP to spike transformation, the selectivity index was, on average, doubled. However, the degree of the selectivity improvement in individual cells was very different, varying from cases in which highly selective output was created from a poorly selective input and thus selectivity was greatly improved, to little or no improvement in other neurons. The improvement of selectivity was not correlated with resting membrane potential, threshold for action potential generation, background discharge rate or amplitude of optimal PSP response. Further, no systematic difference was found between simple and complex cells in the input-output relations, indicating that the 'tip of the iceberg' effect on shaping the response selectivity was cell specific, but not cell type specific. This supports the notion that multiple mechanisms are responsible for generation of the response selectivity, and that the contribution of any particular mechanism may vary from one cell to the other. The heterogeneity of the input-output relations in visual cortical cells could indicate different functions of cells in the cortical network; some cells are creating selectivity de novo, the function of other neurons probably being repetition and amplification of the selected signal and arrangement of the output of a whole column.

Action Potentials↗

Structure and dynamics of receptive fields in the visual cortex of the cat (area 18) and the influence of GABAergic inhibition.

Receptive fields (RFs) in the visual cortex are characterized by spatiotemporal profiles that have been described in detail for area 17 simple cells. In this study, we analyse spatial and temporal RF properties of simple and complex cells in layer II/III of area 18 of the anaesthetized adult cat, using the reverse correlation method with brief 50 ms presentations of flashing bright and dark bars. Stimuli were presented with preferred orientation as previously determined by moving bars. Simple cell RFs were characterized by spatially and temporally separable ON and OFF subfields, while in complex cells ON and OFF subfields were superimposed. To discriminate possible contributions of GABAergic inhibition to RF structure and response dynamics in area 18, we have used three-barrelled micropipettes for single cell recordings and microiontophoresis, and have documented ON and OFF responses before, during and after application of bicuculline methiodide for blockade of GABAA receptors. During blockade of GABAergic inhibition, the stimulus-induced and resting discharge frequency increased, and in about 50% of the cells both ON and OFF subfields changed significantly in space and/or time in a reversible manner. In space, blockade of inhibition widened RF subfields, whereas in time, it shortened the duration of the excitatory cell response in simple and complex cells. ON and OFF subfields separated in space and time (simple cells), or time (complex cells) became less isolated or even superimposed. The results indicate substantial local inhibitory processing contributing to spatiotemporal RF properties in layers II/III of area 18 of the cat.

Animals↗

Fluorometric measurement of the intracellular free Ca(2+)-concentration in the ciliate Didinium nasutum using Fura-2.

We developed an experimental approach to measure somatic and ciliary Ca(2+)-signals in the ciliate Didinium under voltage clamp conditions using the dye Fura-2. Intracellular pressure injection of Fura-2 molecules did not alter electrophysiological membrane properties besides an expected buffering effect. The intracellular free Ca(2+)-concentration was determined at 2 x 10(-7) M. During membrane excitation, this resting value increased in the cilia; a quantification was not feasible. Within the cell soma, however, the Ca(2+)-level was unchanged within the physiological range of the membrane potential (-70 mV to 0 mV). Increasing the driving force for Ca(2+)-ions via strong hyperpolarization (potentials negative to -200 mV) a centripetal increase in the somatic Ca2+ concentration was found. Our results support the hypothesis that Ca2+ is the intracellular messenger in rapid electromotor coupling in ciliates.

Animals↗

Voltage-dependence of ciliary activity in the ciliate Didinium nasutum

In the gymnostome ciliate Didinium nasutum, swimming behaviour depends upon the cyclic activity of about 3000 cilia. The normal beating mode, resulting in forward swimming of the cell, is characterized by a posteriad effective beat (18 left of the longitudinal axis) at a frequency of approximately 15 Hz. Activation of depolarization-sensitive ciliary Ca2+ channels leads to an increase in intracellular Ca2+ concentration and a change in the beating mode. Following rapid reorientation, the effective stroke is anteriad (24 ° right of the longitudinal axis) and the beating frequency is about 26 Hz, resulting in fast backward swimming of the cell. In response to minor depolarizations, and hence small increases in cytoplasmic Ca2+ concentration, the cilia inactivate. Frequency increase and reversal in beat orientation share a single threshold level of membrane potential, since both changes of the beating mode occur simultaneously.

Journal Article↗

Ciliary beating in three dimensions: steps of a quantitative description.

We document a novel approach for quantitative assessment of ciliary activity, exemplified in rapid three-dimensional cyclic motion of the frontal cirri of Stylonychia. Cells held under voltage-clamp control are stimulated by step pulses to elicit reproducible hyperpolarization- or depolarization-induced ciliary motor responses. High-speed video recording at 200 fields per second is used for imaging ciliary organelles of the same cell in two perspectives: the axial view and, following cell rotation by 90 degrees, the lateral view. From video sequences of typically 1 s, the contours of the cirral images are determined and digitized. Computer programs are established to (1) reduce an observed image to a "ciliary axis", (2) sort series of axes by template to generate an averaged ciliary cycle in 2D-projection, and (3) to associate the generalized axial and lateral 2D-images for generation of a sequence of three-dimensional images, which quantitatively represent the cycle in space and time. The method allows us to produce predetermined perspectives of images selected from the ciliary cycle, and to generate stereo views for graphical representation of ciliary motion. The approach includes a potential for extraction of the complete microtubular sliding program of a cilium under reproducible electric stimulation of the ciliary membrane.

Animals↗

Changes in voltage-dependent calcium currents during the cell cycle of the ciliate Stylonychia.

Electrophysiological properties of the hypotrichous ciliate Stylonychia mytilus were studied at two stages of its cell cycle: within 30 min after cell division and several hours thereafter. The action potential wave form, and the relative amount of two voltage-dependent calcium inward currents are significantly different in 'young' daughter cells as compared with 'adult' cells. The ratio between total inward and outward current is also larger in 'young' cells. The results provide evidence that during its cell cycle Stylonychia undergoes qualitative developmental changes with respect to its ionic channels in the membrane. These changes may explain the different cell behaviour observed up to 1 h after cell division.

Action Potentials↗

Messenger role of calcium in ciliary electromotor coupling: a reassessment.

Electrophysiological and cell reactivation studies in Paramecium and other ciliates have established that depolarizing stimulation opens voltage-sensitive ciliary Ca2+ channels leading to an elevation in intraciliary Ca2+, a rapid 'reversal' in sliding-microtubule based ciliary activity and backward swimming. Regulation of cilia by hyperpolarization modulates the pitch and rate of forward locomotion. The control of this predominant behaviour has been a matter of controversy because ciliary conductances do not change with negative shifts from the resting potential. Recordings of ciliary responses during electrophysiological manipulation of the Ca driving force in the ciliates Stylonychia and Didinium now suggests that a crucial step in hyperpolarization-induced ciliary activation (HCA) is a reduction in intraciliary Ca2+ from a resting steady-state level. The data are discussed with respect to previous hypotheses for the regulation of HCA.

Animals↗