Evaluation of the Ca2+ Concentration in Purified Nerve Terminals: Relationship Between Ca2+ Homeostasis and Synaptosomal Preparation
- 1 December 1988
- journal article
- research article
- Published by Wiley in Journal of Neurochemistry
- Vol. 51 (6) , 1667-1674
- https://doi.org/10.1111/j.1471-4159.1988.tb01143.x
Abstract
The presynaptic Ca2+ concentration ([Ca]i) was evaluated by studying intracellular free Ca2+ with quin-2 and fura-2 in synaptosomal preparations. The synaptosomal preparations were purified with hyperosmotic (sucrose) and isoosmotic (Percoll) density gradient centrifugation. Synaptosomes are most viable in the heavier fractions of the density gradients. These synaptosomal fractions exhibit the lowest [Ca]i, [204 ± 2 nM for Percoll (C-band) synaptosomes, loaded at 30°C with the acetoxymethyl ester of fura-2 (fura-2-AM)], a high stability during prolonged incubations at 37°C, and a more potent response to membrane depolarization by elevated extracellular [K+]. [Ca]i measurement was critically dependent on dye loading, calibration, type of dye used, synaptosomal preparation, and incubation temperature (30° or 37°C). Loading quin-2 in synaptosomes inserts a considerable buffer component in the synaptosomal [Ca]i regulation, and consequently there is a quin-2 dependency of [Ca]i, independent of endogenous heavy metal ions. Use of fura-2 is preferable in synaptosomes, although above a critical fura2-AM/protein ratio during loading ester hydrolysis is not complete, giving rise to errors in [Ca]i determination. Ionomycin is a selective tool to detect the presence of partially hydrolyzed esters and saturate indicators in the cytosol with Ca2+ for calibration. Parallel studies on lactate dehydrogenase and fura-2 fluorescence indicate that synaptosomal viability is very sensitive to prolonged incubations at 37°C. This study shows the applicability of measuring steady-state [Ca]i and dynamic [Ca]i changes quantitatively in fura-2-loaded synaptosomes. The possible involvement of different synaptosomal pools to explain the divergence in [Ca]i between different preparations and the interpretation in physiological terms of [Ca]i measured in synaptosomes are discussed.Keywords
This publication has 30 references indexed in Scilit:
- Intractable Unphysiologically Low Adenylate Energy Charge Values in Synaptosome Fractions: An Explanatory Hypothesis Based on the Fraction's HeterogeneityJournal of Neurochemistry, 2006
- Dimethyl sulfoxide increases cytoplasmic Ca2+ concentration and inhibits parathyroid hormone release in normal bovine and pathological human parathyroid cellsBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1987
- The estimation of free calcium within synaptosomes and mitochondria with fura-2; comparison to quin-2Neurochemistry International, 1987
- Quantitative measurements of the cytosolic Ca2+ activity within isolated guinea pig nerve-endings using entrapped arsenazo III and quin2Biochimica et Biophysica Acta (BBA) - Biomembranes, 1986
- Intracellular Ca indicator Quin-2 inhibits Ca2+ inflow via Nai/Cao exchange in squid axonNature, 1985
- Rapid Preparation of Synaptosomes from Mammalian Brain Using Nontoxic Isoosmotic Gradient Material (Percoll)Journal of Neurochemistry, 1984
- Qualitative measurements of cytosolic calcium ion concentration within isolated Guinea pig nerve endings using entrapped arsenazo IIIBiochimica et Biophysica Acta (BBA) - Biomembranes, 1983
- Calcium homeostasis in intact lymphocytes: cytoplasmic free calcium monitored with a new, intracellularly trapped fluorescent indicator.The Journal of cell biology, 1982
- Intrasynaptosomal compartmentation of calcium during depolarization-induced calcium uptake across the plasma membraneBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976