Computational properties of peri-dendritic calcium fluctuations.
نویسندگان
چکیده
Using a model of the extracellular space, we show how external calcium fluctuations, engendered during normal neural activity, can act as a rapid information-bearing signal in nervous systems. We demonstrate that action potentials propagating along a dendrite can induce large peri-dendritic calcium fluctuations, lowering significantly the external calcium available to overlying presynaptic terminals. The geometrical distribution of active calcium sinks critically influences the time and spatial extent of fluctuations in external calcium. In particular, clusters of coactive dendrites can prolong and amplify an external calcium fluctuation. This latter effect provides a natural substrate for a computational mechanism that locates specific volumes of neural tissue on rapid time scales. Such an interpretation suggests that the detailed structure of the extracellular space, in combination with the three-dimensional distribution of active calcium sinks, may play a role in neural information processing.
منابع مشابه
Stochastic calcium mechanisms cause dendritic calcium spike variability.
Bursts of dendritic calcium spikes play an important role in excitability and synaptic plasticity in many types of neurons. In single Purkinje cells, spontaneous and synaptically evoked dendritic calcium bursts come in a variety of shapes with a variable number of spikes. The mechanisms causing this variability have never been investigated thoroughly. In this study, a detailed computational mod...
متن کاملDendritic spikes and their influence on extracellular calcium signaling.
Extracellular calcium is critical for many neural functions, including neurotransmission, cell adhesion, and neural plasticity. Experiments have shown that normal neural activity is associated with changes in extracellular calcium, which has motivated recent computational work that employs such fluctuations in an information-bearing role. This possibility suggests that a new style of computing ...
متن کاملElectrical Advantages of Dendritic Spines
Many neurons receive excitatory glutamatergic input almost exclusively onto dendritic spines. In the absence of spines, the amplitudes and kinetics of excitatory postsynaptic potentials (EPSPs) at the site of synaptic input are highly variable and depend on dendritic location. We hypothesized that dendritic spines standardize the local geometry at the site of synaptic input, thereby reducing lo...
متن کاملDendritic integration and its role in computing image velocity.
The mechanisms underlying visual motion detection can be studied simultaneously in different cell compartments in vivo by using calcium as a reporter of the spatiotemporal activity distribution in single motion-sensitive cells of the fly. As predicted by the Reichardt model, local dendritic calcium signals are found to indicate the direction and velocity of pattern motion but are corrupted by s...
متن کاملIn vivo, in vitro, and computational analysis of dendritic calcium currents in thalamic reticular neurons.
Thalamic reticular (RE) neurons are involved in the genesis of synchronized thalamocortical oscillations, which depend in part on their complex bursting properties. We have investigated the intrinsic properties of RE cells using computational models based on morphological and electrophysiological data. Simulations of a reconstructed RE cells were compared directly with recordings from the same ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The Journal of neuroscience : the official journal of the Society for Neuroscience
دوره 18 21 شماره
صفحات -
تاریخ انتشار 1998