191 research outputs found
Studies on conjugation of Spirogyra using monoclonal culture
We succeeded in inducing conjugation of Spirogyracastanacea by incubating algal filaments on agar plate. Conjugation could be induced using clone culture. The scalariform conjugation was generally observed, while lateral conjugation was rarely. When two filaments formed scalariform conjugation, all cells of one filament behaved as male and those of other filament did as female. Very rarely, however, zygospores were formed in both of pair filaments. The surface of conjugation tube was stained with fluorescently labeled-lectins, such as Bandeiraea (Griffonia) simplicifolia lectin (BSL-I) and jacalin. BSL-I strongly stained the conjugation tubes, while weakly did the cell surface of female gamete first and then that of male gamete. Jacalin stained mainly the conjugation tubes. Addition of jacalin inhibited the formation of papilla, suggesting some important role of jacalin-binding material at the initial step of formation of the conjugation tubes
Design for a Darwinian Brain: Part 1. Philosophy and Neuroscience
Physical symbol systems are needed for open-ended cognition. A good way to
understand physical symbol systems is by comparison of thought to chemistry.
Both have systematicity, productivity and compositionality. The state of the
art in cognitive architectures for open-ended cognition is critically assessed.
I conclude that a cognitive architecture that evolves symbol structures in the
brain is a promising candidate to explain open-ended cognition. Part 2 of the
paper presents such a cognitive architecture.Comment: Darwinian Neurodynamics. Submitted as a two part paper to Living
Machines 2013 Natural History Museum, Londo
Theory of Interaction of Memory Patterns in Layered Associative Networks
A synfire chain is a network that can generate repeated spike patterns with
millisecond precision. Although synfire chains with only one activity
propagation mode have been intensively analyzed with several neuron models,
those with several stable propagation modes have not been thoroughly
investigated. By using the leaky integrate-and-fire neuron model, we
constructed a layered associative network embedded with memory patterns. We
analyzed the network dynamics with the Fokker-Planck equation. First, we
addressed the stability of one memory pattern as a propagating spike volley. We
showed that memory patterns propagate as pulse packets. Second, we investigated
the activity when we activated two different memory patterns. Simultaneous
activation of two memory patterns with the same strength led the propagating
pattern to a mixed state. In contrast, when the activations had different
strengths, the pulse packet converged to a two-peak state. Finally, we studied
the effect of the preceding pulse packet on the following pulse packet. The
following pulse packet was modified from its original activated memory pattern,
and it converged to a two-peak state, mixed state or non-spike state depending
on the time interval
Sparse and Dense Encoding in Layered Associative Network of Spiking Neurons
A synfire chain is a simple neural network model which can propagate stable
synchronous spikes called a pulse packet and widely researched. However how
synfire chains coexist in one network remains to be elucidated. We have studied
the activity of a layered associative network of Leaky Integrate-and-Fire
neurons in which connection we embed memory patterns by the Hebbian Learning.
We analyzed their activity by the Fokker-Planck method. In our previous report,
when a half of neurons belongs to each memory pattern (memory pattern rate
), the temporal profiles of the network activity is split into
temporally clustered groups called sublattices under certain input conditions.
In this study, we show that when the network is sparsely connected (),
synchronous firings of the memory pattern are promoted. On the contrary, the
densely connected network () inhibit synchronous firings. The sparseness
and denseness also effect the basin of attraction and the storage capacity of
the embedded memory patterns. We show that the sparsely(densely) connected
networks enlarge(shrink) the basion of attraction and increase(decrease) the
storage capacity
Universal features of correlated bursty behaviour
Inhomogeneous temporal processes, like those appearing in human
communications, neuron spike trains, and seismic signals, consist of
high-activity bursty intervals alternating with long low-activity periods. In
recent studies such bursty behavior has been characterized by a fat-tailed
inter-event time distribution, while temporal correlations were measured by the
autocorrelation function. However, these characteristic functions are not
capable to fully characterize temporally correlated heterogenous behavior. Here
we show that the distribution of the number of events in a bursty period serves
as a good indicator of the dependencies, leading to the universal observation
of power-law distribution in a broad class of phenomena. We find that the
correlations in these quite different systems can be commonly interpreted by
memory effects and described by a simple phenomenological model, which displays
temporal behavior qualitatively similar to that in real systems
Statistical Significance of Precisely Repeated Intracellular Synaptic Patterns
Can neuronal networks produce patterns of activity with millisecond accuracy? It may seem unlikely, considering the probabilistic nature of synaptic transmission. However, some theories of brain function predict that such precision is feasible and can emerge from the non-linearity of the action potential generation in circuits of connected neurons. Several studies have presented evidence for and against this hypothesis. Our earlier work supported the precision hypothesis, based on results demonstrating that precise patterns of synaptic inputs could be found in intracellular recordings from neurons in brain slices and in vivo. To test this hypothesis, we devised a method for finding precise repeats of activity and compared repeats found in the data to those found in surrogate datasets made by shuffling the original data. Because more repeats were found in the original data than in the surrogate data sets, we argued that repeats were not due to chance occurrence. Mokeichev et al. (2007) challenged these conclusions, arguing that the generation of surrogate data was insufficiently rigorous. We have now reanalyzed our previous data with the methods introduced from Mokeichev et al. (2007). Our reanalysis reveals that repeats are statistically significant, thus supporting our earlier conclusions, while also supporting many conclusions that Mokeichev et al. (2007) drew from their recent in vivo recordings. Moreover, we also show that the conditions under which the membrane potential is recorded contributes significantly to the ability to detect repeats and may explain conflicting results. In conclusion, our reevaluation resolves the methodological contradictions between Ikegaya et al. (2004) and Mokeichev et al. (2007), but demonstrates the validity of our previous conclusion that spontaneous network activity is non-randomly organized
Of Mice and Men, and Chandeliers
How does the human neocortex reliably propagate information through neural circuits? One mechanism appears to involve relying on strong connections from pyramidal neurons to interneurons and a depolarizing action of cortical chandelier cells
Complex Events Initiated by Individual Spikes in the Human Cerebral Cortex
Synaptic interactions between neurons of the human cerebral cortex were not directly studied to date. We recorded the first dataset, to our knowledge, on the synaptic effect of identified human pyramidal cells on various types of postsynaptic neurons and reveal complex events triggered by individual action potentials in the human neocortical network. Brain slices were prepared from nonpathological samples of cortex that had to be removed for the surgical treatment of brain areas beneath association cortices of 58 patients aged 18 to 73 y. Simultaneous triple and quadruple whole-cell patch clamp recordings were performed testing mono- and polysynaptic potentials in target neurons following a single action potential fired by layer 2/3 pyramidal cells, and the temporal structure of events and underlying mechanisms were analyzed. In addition to monosynaptic postsynaptic potentials, individual action potentials in presynaptic pyramidal cells initiated long-lasting (37 ± 17 ms) sequences of events in the network lasting an order of magnitude longer than detected previously in other species. These event series were composed of specifically alternating glutamatergic and GABAergic postsynaptic potentials and required selective spike-to-spike coupling from pyramidal cells to GABAergic interneurons producing concomitant inhibitory as well as excitatory feed-forward action of GABA. Single action potentials of human neurons are sufficient to recruit Hebbian-like neuronal assemblies that are proposed to participate in cognitive processes
An Approach for Reliably Investigating Hippocampal Sharp Wave-Ripples In Vitro
Among the various hippocampal network patterns, sharp wave-ripples (SPW-R) are currently the mechanistically least understood. Although accurate information on synaptic interactions between the participating neurons is essential for comprehensive understanding of the network function during complex activities like SPW-R, such knowledge is currently notably scarce. counterpart. We show that slice storage in the interface chamber close to physiological temperature is the required condition to preserve network integrity that is necessary for the generation of SPW-R. Moreover, we demonstrate the utility of our method for studying synaptic and network properties of SPW-R, using electrophysiological and imaging methods that can only be applied in the submerged system.The approach presented here demonstrates a reliable and experimentally simple strategy for studying hippocampal sharp wave-ripples. Given its utility and easy application we expect our model to foster the generation of new insight into the network physiology underlying SPW-R
Specific In Vivo Staining of Astrocytes in the Whole Brain after Intravenous Injection of Sulforhodamine Dyes
Fluorescent staining of astrocytes without damaging or interfering with normal brain functions is essential for intravital microscopy studies. Current methods involved either transgenic mice or local intracerebral injection of sulforhodamine 101. Transgenic rat models rarely exist, and in mice, a backcross with GFAP transgenic mice may be difficult. Local injections of fluorescent dyes are invasive. Here, we propose a non-invasive, specific and ubiquitous method to stain astrocytes in vivo. This method is based on iv injection of sulforhodamine dyes and is applicable on rats and mice from postnatal age to adulthood. The astrocytes staining obtained after iv injection was maintained for nearly half a day and showed no adverse reaction on astrocytic calcium signals or electroencephalographic recordings in vivo. The high contrast of the staining facilitates the image processing and allows to quantify 3D morphological parameters of the astrocytes and to characterize their network. Our method may become a reference for in vivo staining of the whole astrocytes population in animal models of neurological disorders
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