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      Multiple Modes of Calcium-Induced Calcium Release in Sympathetic Neurons II : A [Ca 2+] i- and Location-Dependent Transition from Endoplasmic Reticulum Ca Accumulation to Net Ca Release

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          Abstract

          CICR from an intracellular store, here directly characterized as the ER, usually refers to net Ca 2+ release that amplifies evoked elevations in cytosolic free calcium ([Ca 2+] i). However, the companion paper (Albrecht, M.A., S.L. Colegrove, J. Hongpaisan, N.B. Pivovarova, S.B. Andrews, and D.D. Friel. 2001. J. Gen. Physiol. 118:83–100) shows that in sympathetic neurons, small [Ca 2+] i elevations evoked by weak depolarization stimulate ER Ca accumulation, but at a rate attenuated by activation of a ryanodine-sensitive CICR pathway. Here, we have measured depolarization-evoked changes in total ER Ca concentration ([Ca] ER) as a function of [Ca 2+] i, and found that progressively larger [Ca 2+] i elevations cause a graded transition from ER Ca accumulation to net release, consistent with the expression of multiple modes of CICR. [Ca] ER is relatively high at rest (12.8 ± 0.9 mmol/kg dry weight, mean ± SEM) and is reduced by thapsigargin or ryanodine (5.5 ± 0.7 and 4.7 ± 1.1 mmol/kg, respectively). [Ca] ER rises during weak depolarization (to 17.0 ± 1.6 mmol/kg over 120s, [Ca 2+] i less than ∼350 nM), changes little in response to stronger depolarization (12.1 ± 1.1 mmol/kg, [Ca 2+] i ∼700 nM), and declines (to 6.5 ± 1.0 mmol/kg) with larger [Ca 2+] i elevations (>1 μM) evoked by the same depolarization when mitochondrial Ca 2+ uptake is inhibited (FCCP). Thus, net ER Ca 2+ transport exhibits a biphasic dependence on [Ca 2+] i. With mitochondrial Ca 2+ uptake enabled, [Ca] ER rises after repolarization (to 16.6 ± 1.8 mmol/kg at 15 min) as [Ca 2+] i falls within the permissive range for ER Ca accumulation over a period lengthened by mitochondrial Ca 2+ release. Finally, although spatially averaged [Ca] ER is unchanged during strong depolarization, net ER Ca 2+ release still occurs, but only in the outermost ∼5-μm cytoplasmic shell where [Ca 2+] i should reach its highest levels. Since mitochondrial Ca accumulation occurs preferentially in peripheral cytoplasm, as demonstrated here by electron energy loss Ca maps, the Ca content of ER and mitochondria exhibit reciprocal dependencies on proximity to sites of Ca 2+ entry, possibly reflecting indirect mitochondrial regulation of ER Ca 2+ transport.

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          CREB phosphorylation and dephosphorylation: a Ca(2+)- and stimulus duration-dependent switch for hippocampal gene expression.

          While changes in gene expression are critical for many brain functions, including long-term memory, little is known about the cellular processes that mediate stimulus-transcription coupling at central synapses. In studying the signaling pathways by which synaptic inputs control the phosphorylation state of cyclic AMP-responsive element binding protein (CREB) and determine expression of CRE-regulated genes, we found two important Ca2+/calmodulin (CaM)-regulated mechanisms in hippocampal neurons: a CaM kinase cascade involving nuclear CaMKIV and a calcineurin-dependent regulation of nuclear protein phosphatase 1 activity. Prolongation of the synaptic input on the time scale of minutes, in part by an activity-induced inactivation of calcineurin, greatly extends the period over which phospho-CREB levels are elevated, thus affecting induction of downstream genes.
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            Molecular and cellular physiology of intracellular calcium stores.

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              Glutamate-induced neuron death requires mitochondrial calcium uptake.

              We have investigated the role of mitochondrial calcium buffering in excitotoxic cell death. Glutamate acts at NMDA receptors in cultured rat forebrain neurons to increase the intracellular free calcium concentration. Although concurrent inhibition of mitochondrial calcium uptake substantially enhanced this cytoplasmic calcium increase, it significantly reduced glutamate-stimulated neuronal cell death. Mitochondrial inhibition did not affect nitric oxide production or MAP kinase phosphorylation, which have been proposed to mediate excitotoxicity. These results indicate that very high levels of cytoplasmic calcium are not necessarily toxic to forebrain neurons, and that potential-driven uptake of calcium into mitochondria is required to trigger NMDA-receptor-stimulated neuronal death.
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                Author and article information

                Contributors
                Journal
                J Gen Physiol
                The Journal of General Physiology
                The Rockefeller University Press
                0022-1295
                1540-7748
                1 July 2001
                : 118
                : 1
                : 101-112
                Affiliations
                [a ]Laboratory of Neurobiology, National Institute of Neurological Disorders and Stroke
                [b ]Bioengineering and Physical Science Program, Office of the Director, National Institutes of Health, Bethesda, MD 20892
                [c ]Department of Neuroscience, Case Western Reserve University, Cleveland, OH 44106
                Article
                8322
                2233743
                11429447
                152aa124-6898-4a2e-a1fe-66d5d767b5c7
                © 2001 The Rockefeller University Press
                History
                : 6 October 2000
                : 15 May 2001
                : 17 May 2001
                Categories
                Original Article

                Anatomy & Physiology
                ryanodine,calcium signaling,electron energy loss spectrum imaging,electron probe x-ray microanalysis,mitochondria

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