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Functional Compatibility Between Purkinje Cell Axon Branches and Their Target Neurons in the Cerebellum

Overview
Journal Oncotarget
Specialty Oncology
Date 2017 Oct 27
PMID 29069799
Citations 10
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Abstract

A neuron sprouts an axon, and its branches to innervate many target neurons that are divergent in their functions. In order to efficiently regulate the diversified cells, the axon branches should differentiate functionally to be compatible with their target neurons, i.e., a function compatibility between presynaptic and postsynaptic partners. We have examined this hypothesis by using electrophysiological method in the cerebellum, in which the main axon of Purkinje cell projected to deep nucleus cells and the recurrent axons innervated the adjacent Purkinje cells. The fidelity of spike propagation is superior in the recurrent branches than the main axon. The capabilities of encoding spikes and processing GABAergic inputs are advanced in Purkinje cells versus deep nucleus cells. The functional differences among Purkinje's axonal branches and their postsynaptic neurons are preset by the variable dynamics of their voltage-gated sodium channels. In addition, activity strengths between presynaptic and postsynaptic partners are proportionally correlated, i.e., active axonal branches innervate active target neurons, or vice versa. The physiological impact of the functional compatibility is to make the neurons in their circuits to be activated appropriately. In conclusion, each cerebellar Purkinje cell sprouts the differentiated axon branches to be compatible with the diversified target cells in their functions, in order to construct the homeostatic and efficient units for their coordinated activity in neural circuits.

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References
1.
Zhu Z, Wang G, Ma K, Cui S, Wang J . GABAergic neurons in nucleus accumbens are correlated to resilience and vulnerability to chronic stress for major depression. Oncotarget. 2017; 8(22):35933-35945. PMC: 5482628. DOI: 10.18632/oncotarget.16411. View

2.
Monsivais P, Clark B, Roth A, Hausser M . Determinants of action potential propagation in cerebellar Purkinje cell axons. J Neurosci. 2005; 25(2):464-72. PMC: 6725482. DOI: 10.1523/JNEUROSCI.3871-04.2005. View

3.
Stuart G, Hausser M . Initiation and spread of sodium action potentials in cerebellar Purkinje cells. Neuron. 1994; 13(3):703-12. DOI: 10.1016/0896-6273(94)90037-x. View

4.
Hockberger P, Tseng H, Connor J . Development of rat cerebellar Purkinje cells: electrophysiological properties following acute isolation and in long-term culture. J Neurosci. 1989; 9(7):2258-71. PMC: 6569754. View

5.
Ma K, Xu A, Cui S, Sun M, Xue Y, Wang J . Impaired GABA synthesis, uptake and release are associated with depression-like behaviors induced by chronic mild stress. Transl Psychiatry. 2016; 6(10):e910. PMC: 5315548. DOI: 10.1038/tp.2016.181. View