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Fluorescence lifetime imaging reveals regulation of presynaptic Ca 2+ by glutamate uptake and mGluRs, but not somatic voltage in cortical neurons
Author(s) -
Tyurikova Olga,
Zheng Kaiyu,
Nicholson Elizabeth,
Timofeeva Yulia,
Semyanov Alexey,
Volynski Kirill E.,
Rusakov Dmitri A.
Publication year - 2021
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.15094
Subject(s) - glutamate receptor , neuroscience , metabotropic glutamate receptor , hyperpolarization (physics) , biophysics , biology , depolarization , calcium imaging , calcium , chemistry , receptor , biochemistry , organic chemistry , nuclear magnetic resonance spectroscopy
Brain function relies on vesicular release of neurotransmitters at chemical synapses. The release probability depends on action potential‐evoked presynaptic Ca 2+ entry, but also on the resting Ca 2+ level. Whether these basic aspects of presynaptic calcium homeostasis show any consistent trend along the axonal path, and how they are controlled by local network activity, remains poorly understood. Here, we take advantage of the recently advanced FLIM‐based method to monitor presynaptic Ca 2+ with nanomolar sensitivity. We find that, in cortical pyramidal neurons, action potential‐evoked calcium entry (range 10–300 nM), but not the resting Ca 2+ level (range 10–100 nM), tends to increase with higher order of axonal branches. Blocking astroglial glutamate uptake reduces evoked Ca 2+ entry but has little effect on resting Ca 2+ whereas both appear boosted by the constitutive activation of group 1/2 metabotropic glutamate receptors. We find no consistent effect of transient somatic depolarization or hyperpolarization on presynaptic Ca 2+ entry or its basal level. The results unveil some key aspects of presynaptic machinery in cortical circuits, shedding light on basic principles of synaptic connectivity in the brain.