Literature DB >> 11243935

Calcium buffering and protection from excitotoxic cell death by exogenous calbindin-D28k in HEK 293 cells.

G L Rintoul1, L A Raymond, K G Baimbridge.   

Abstract

Calbindin-D28k (CaBP) is a calcium-binding protein found in specific neuronal populations in the mammalian brain that, as a result of its proposed calcium-buffering action, may protect neurons against potentially harmful increases in intracellular calcium. We have stably transfected HEK 293 cells with recombinant human CaBP in order to determine the influence of this protein upon transient increases in intracellular ionic calcium concentration ([Ca(2+)](i)) induced either by transient transfection of the NR1 and NR2A subunits of the N-methyl-D-aspartate (NMDA) receptor and brief exposure to glutamate, photolysis of the caged calcium compound NP-EGTA, or exposure to the Ca(2+)]-ionophore 4-Br-A23187. The presence of CaBP did not significantly reduce the peak [Ca(2+)](i)stimulated by glutamate activation of NMDA receptors but significantly prolonged the recovery to baseline values. Flash photolysis of NP-EGTA in control cells resulted in an almost instantaneous increase in [Ca(2+)](i)followed by a bi-exponential recovery to baseline values. In cells stably expressing CaBP, the peak [Ca(2+)](i)levels were not statistically different from the controls, however, there was a significant prolongation of the initial portion of the slow recovery phase. In cells exposed to 4-Br-A23187, the presence of CaBP significantly reduced the rate of rise of [Ca(2+)](i), reduced the peak response, slowed the rate of recovery, and reduced the depolarization of mitochondria. In studies of delayed, Ca(2+)]-dependent cell death, CaBP transfected cells exhibited enhanced survival 24h after a 1-h exposure to 200 microM NMDA. However, necrotic cell death observed after the first 6h was not prevented by the presence of CaBP. These results provide direct evidence for a Ca(2+)-buffering effect of CaBP which serves to limit Ca(2+)entry and the depolarization of mitochondria, thereby protecting cells from death mediated most likely by apoptosis. Copyright 2001 Harcourt Publishers Ltd.

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Year:  2001        PMID: 11243935     DOI: 10.1054/ceca.2000.0190

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  19 in total

1.  Intracellular calcium ion response to glucose in beta-cells of calbindin-D28k nullmutant mice and in betaHC13 cells overexpressing calbindin-D28k.

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2.  Climbing fibers induce microRNA transcription in cerebellar Purkinje cells.

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Journal:  Neuroscience       Date:  2010-09-25       Impact factor: 3.590

3.  In vivo AAV-mediated expression of calbindin-D₂₈k in rat basal forebrain cholinergic neurons.

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Journal:  J Neurosci Methods       Date:  2012-09-27       Impact factor: 2.390

4.  Characterisation of transverse slice culture preparations of postnatal rat spinal cord: preservation of defined neuronal populations.

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Journal:  Histochem Cell Biol       Date:  2005-05-12       Impact factor: 4.304

5.  Downregulation of calbindin 1, a calcium-binding protein, reduces the proliferation of osteosarcoma cells.

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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-09-26       Impact factor: 6.237

Review 7.  Mitochondrial calcium function and dysfunction in the central nervous system.

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Journal:  ACS Chem Neurosci       Date:  2012-11-21       Impact factor: 4.418

Review 9.  What can we learn about stroke from retinal ischemia models?

Authors:  Philippe M D'Onofrio; Paulo D Koeberle
Journal:  Acta Pharmacol Sin       Date:  2012-12-03       Impact factor: 6.150

10.  Loss of calbindin-D28K is associated with the full range of tangle pathology within basal forebrain cholinergic neurons in Alzheimer's disease.

Authors:  Saman S Ahmadian; Aras Rezvanian; Melanie Peterson; Sandra Weintraub; Eileen H Bigio; Marek-Marsel Mesulam; Changiz Geula
Journal:  Neurobiol Aging       Date:  2015-09-06       Impact factor: 4.673

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