Investigation of detector properties of neurons in the visual system of the rabbit

Responses of neurons in the superior colliculi and visual cortex of rabbits to a black and white boundary moving in different directions were investigated. Neurons responding clearly to presentation of the black and white boundary moving in one direction (movement in the opposite direction led to inhibition of spontaneous activity) and neurons giving well-defined maximal responses to movement of this boundary in 2 or 3 directions were found in the superior colliculi. Neurons with a marked maximal response to the stimulus moving in 1 or 2 directions were found in the visual cortex. Nembutal has a powerful effect on the quantitative detector properties of visual cortical neurons and sometimes may completely inhibit unit activity.V. Kapsukas Vilnius State University. Translated from Neirofiziologiya, Vol. 4, No. 1, pp. 61–67, January–February, 1972.     

Plasma membrane calcium pump activity is affected by the membrane protein concentration: evidence for the involvement of the actin cytoskeleton

Plasma membrane calcium pumps (PMCAs) are integral membrane proteins that actively expel Ca(2+) from the cell. Specific Ca(2+)-ATPase activity of erythrocyte membranes increased steeply up to 1.5-5 times when the membrane protein concentration decreased from 50 microg/ml to 1 microg/ml. The activation by dilution was also observed for ATP-dependent Ca(2+) uptake into vesicles from Sf9 cells over-expressing the PMCA 4b isoform, confirming that it is a property of the PMCA. Dilution of the protein did not modify the activation by ATP, Ca(2+) or Ca(2+)-calmodulin. Treatment with non-ionic detergents did not abolish the dilution effect, suggesting that it was not due to resealing of the membrane vesicles. Pre-incubation of erythrocyte membranes with Cytochalasin D under conditions that promote actin polymerization abolished the dilution effect. Highly-purified, micellar PMCA showed no dilution effect and was not affected by Cytochalasin D. Taken together, these results suggest that the concentration-dependent behavior of the PMCA activity was due to interactions with cytoskeletal proteins. The dilution effect was also observed with different PMCA isoforms, indicating that this is a general phenomenon for all PMCAs.     

Heterogeneity of neuron populations with complex receptive fields in the cat visual cortex

The selectivity of striate neurons with complex receptive fields to the orientation, direction, and velocity of movement of various stimuli was investigated in unanesthetized and uncurarized cats. On the basis of all characteristics obtained by the study of single-unit responses to a stationary flickering slit, a moving spot of light, and a moving oriented stimulus, four groups of complex neurons were distinguished. The characteristics of group I neurons indicate a mechanism of orientation selectivity in the organization of their receptive fields, group IV neurons have a mechanism of directional selectivity, and neurons of groups II and III possess both mechanisms. The existence of separate neuronal systems coding the orientation and direction of stimulus movement is suggested.V. Kapsukas State University, Vilnius. Translated from Neirofiziologiya, Vol. 11, No. 2, pp. 109–116, March–April, 1979.     

Differential Effects of G- and F-Actin on the Plasma Membrane Calcium Pump Activity

We have previously shown that plasma membrane calcium ATPase (PMCA) pump activity is affected by the membrane protein concentration (Vanagas et al., Biochim Biophys Acta 1768:1641–1644, 2007). The results of this study provided evidence for the involvement of the actin cytoskeleton. In this study, we explored the relationship between the polymerization state of actin and its effects on purified PMCA activity. Our results show that PMCA associates with the actin cytoskeleton and this interaction causes a modulation of the catalytic activity involving the phosphorylated intermediate of the pump. The state of actin polymerization determines whether it acts as an activator or an inhibitor of the pump: G-actin and/or short oligomers activate the pump, while F-actin inhibits it. The effects of actin on PMCA are the consequence of direct interaction as demonstrated by immunoblotting and cosedimentation experiments. Taken together, these findings suggest that interactions with actin play a dynamic role in the regulation of PMCA-mediated Ca²⁺ extrusion through the membrane. Our results provide further evidence of the activation–inhibition phenomenon as a property of many cytoskeleton-associated membrane proteins where the cytoskeleton is no longer restricted to a mechanical function but is dynamically involved in modulating the activity of integral proteins with which it interacts.     

Plasma membrane calcium pump activity is affected by the membrane protein concentration: Evidence for the involvement of the actin cytoskeleton

Plasma membrane calcium pumps (PMCAs) are integral membrane proteins that actively expel Ca²⁺ from the cell. Specific Ca²⁺-ATPase activity of erythrocyte membranes increased steeply up to 1.5-5 times when the membrane protein concentration decreased from 50 μg/ml to 1 μg/ml. The activation by dilution was also observed for ATP-dependent Ca²⁺ uptake into vesicles from Sf9 cells over-expressing the PMCA 4b isoform, confirming that it is a property of the PMCA. Dilution of the protein did not modify the activation by ATP, Ca²⁺ or Ca²⁺-calmodulin. Treatment with non-ionic detergents did not abolish the dilution effect, suggesting that it was not due to resealing of the membrane vesicles. Pre-incubation of erythrocyte membranes with Cytochalasin D under conditions that promote actin polymerization abolished the dilution effect. Highly-purified, micellar PMCA showed no dilution effect and was not affected by Cytochalasin D. Taken together, these results suggest that the concentration-dependent behavior of the PMCA activity was due to interactions with cytoskeletal proteins. The dilution effect was also observed with different PMCA isoforms, indicating that this is a general phenomenon for all PMCAs.     

Effects of itaconic acid on neuronal viability and brain mitochondrial functions

Recent studies have identified that under stimulation by bacterial lipopolysaccharide mammalian macrophages produce itaconic acid. Yet, it is unknown whether itaconate has any effect on viability of brain cells. Here we used extracellularly added itaconate to investigate its effects on viability of cerebellar granule cells (CGC) in cultures and respiratory functions of these cells and isolated brain mitochondria. We found that 3–5 mM itaconate had no effect on the viability of neurons, but 10 mM itaconate was toxic and induced neuronal apoptosis. Removal of itaconate after 24 h incubation resulted in further decrease in viability and number of neurons. Respiration of intact neurons was not affected by itaconate, but permeabilized cells as well as isolated brain mitochondria demonstrated decreased rates of respiration in the presence of itaconate. Using isolated adult rat brain mitochondria we found that itaconate decreased mitochondrial phosphorylating respiration, mitochondrial calcium retention capacity, production of reactive oxygen species with Complex I and Complex II substrates as well as inhibition of Complex I, Complex IV and ATP synthase. In conclusion, the results suggest that itaconic acid at millimolar concentrations affects mitochondrial functions and viability of neurons.

     

Bursting activity in visual neurons of the cat cortex during pattern detection

The time course of neuronal response to presentation of a static flashing slit at different angles and both light spots and light strips moving in different directions was investigated in the Clare-Bishop area of the cat cortex. It was found that orientational and directional tuning patterns were mainly determined by the bursting constituent of the response and could be measured according to the number of spikes per burst or the actual number of bursts. A closed-loop model for pattern detection is introduced to shed light on bursting activity.V. Kapsuko State University, Vil'nius. Translated from Neirofiziologiya, Vol. 19, No. 3, pp. 335–343, May–June, 1987.