Literature DB >> 8606791

The use of fura-2 for estimating Ca buffers and Ca fluxes.

E Neher1.   

Abstract

The compound fura-2 (Grynkiewicz et al., J. Biol. Chem. 260, 3440-3450, 1985) is generally known as an indicator dye for measuring the concentration of free calcium ([Ca2+]) inside living cells. It should be appreciated, however, that this is not what it actually is. More accurately, it is a divalent metal ion chelator which changes its fluorescence properties upon complexation. Thus, [Ca2+] has to be inferred indirectly by means of the law of mass action. As a chelator, fura-2 may influence the quantity of interest, the Ca signal. On the other hand, the chelator action may be used for a number of other purposes, some of them more directly related to its molecular properties: as a chelator, competing with endogenous Ca buffers, it can be used to estimate endogenous buffers and their properties. When present at sufficiently high concentration, such that it outcompetes endogenous buffers, fura-2 reports total Ca changes and is a probe for Ca fluxes across the membrane. Here, theory and methodological considerations of such applications of fura-2 will be summarized and results on Ca buffer and Ca flux measurements derived from various methods will be compared.

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Year:  1995        PMID: 8606791     DOI: 10.1016/0028-3908(95)00144-u

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  142 in total

1.  On the characterisation of the mechanism underlying passive activation of the Ca2+ release-activated Ca2+ current ICRAC in rat basophilic leukaemia cells.

Authors:  L Fierro; A B Parekh
Journal:  J Physiol       Date:  1999-10-15       Impact factor: 5.182

2.  The probability of quantal secretion near a single calcium channel of an active zone.

Authors:  M R Bennett; L Farnell; W G Gibson
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

3.  Syntaxin modulation of calcium channels in cortical synaptosomes as revealed by botulinum toxin C1.

Authors:  J B Bergsman; R W Tsien
Journal:  J Neurosci       Date:  2000-06-15       Impact factor: 6.167

4.  Ca2+ influx via the L-type Ca2+ channel during tail current and above current reversal potential in ferret ventricular myocytes.

Authors:  Z Zhou; D M Bers
Journal:  J Physiol       Date:  2000-02-15       Impact factor: 5.182

5.  Apparent intracellular Mg2+ buffering in neurons of the leech Hirudo medicinalis.

Authors:  D Günzel; F Zimmermann; S Durry; W R Schlue
Journal:  Biophys J       Date:  2001-03       Impact factor: 4.033

6.  Effect of changes in action potential shape on calcium currents and transmitter release in a calyx-type synapse of the rat auditory brainstem.

Authors:  J G Borst; B Sakmann
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

7.  Cooperative Ca2+ removal from presynaptic terminals of the spiny lobster neuromuscular junction.

Authors:  K Ohnuma; T Kazawa; S Ogawa; N Suzuki; A Miwa; H Kijima
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

8.  Voltage-dependent conductance changes in the store-operated Ca2+ current ICRAC in rat basophilic leukaemia cells.

Authors:  D Bakowski; A B Parekh
Journal:  J Physiol       Date:  2000-12-01       Impact factor: 5.182

9.  The Lurcher mutation identifies delta 2 as an AMPA/kainate receptor-like channel that is potentiated by Ca(2+).

Authors:  L P Wollmuth; T Kuner; C Jatzke; P H Seeburg; N Heintz; J Zuo
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

10.  Regulation of Ca2+ release by InsP3 in single guinea pig hepatocytes and rat Purkinje neurons.

Authors:  D Ogden; T Capiod
Journal:  J Gen Physiol       Date:  1997-06       Impact factor: 4.086

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