Segregation of calcium signalling mechanisms in magnocellular neurones and terminals
Abstract
Every cell or neuronal type utilizes its own specific organization of its Ca(2+) homeostasis depending on its specific function and its physiological needs. The magnocellular neurones, with their somata situated in the supraoptic and paraventricular nuclei of the hypothalamus and their nerve terminals populating the posterior hypophysis (neural lobe) are a typical and classical example of a neuroendocrine system, and an important experimental model for attempting to understand the characteristics of the neuronal organization of Ca(2+) homeostasis. The magnocellular neurones synthesize, in a cell specific manner, two neurohormones: arginine-vasopressin (AVP) and oxytocin (OT), which can be released, in a strict Ca(2+)-dependent manner, both at the axonal terminals, in the neural lobe, and at the somatodendritic level. The two types of neurones show also distinct type of bioelectrical activity, associated with specific secretory patterns. In these neurones, the Ca(2+) homeostatic pathways such as the Na(+)/Ca(2+) exchanger (NCX), the endoplasmic reticulum (ER) Ca(2+) pump, the plasmalemmal Ca(2+) pump (PMCA) and the mitochondria are acting in a complementary fashion in clearing Ca(2+) loads that follow neuronal stimulation. The somatodendritic AVP and OT release closely correlates with intracellular Ca(2+) dynamics. More importantly, the ER Ca(2+) stores play a major role in Ca(2+) homeostatic mechanism in identified OT neurones. The balance between the Ca(2+) homeostatic systems that are in the supraoptic neurones differ from those active in the terminals, in which mainly Ca(2+) extrusion through the Ca(2+) pump in the plasma membrane and uptake by mitochondria are active. In both AVP and OT nerve terminals, no functional ER Ca(2+) stores can be evidenced experimentally. We conclude that the physiological significance of the complexity of Ca(2+) homeostatic mechanisms in the somatodendritic region of supraoptic neurones and their terminals can be multifaceted, attributable, in major part, to their specialized electrical activity and Ca(2+)-dependent neurohormone release.
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Magnocellular neurons have increased mitochondrial density.
“Previous reports indicate that magnocellular neurons have increased mitochondrial density (Dayanithi et al., 2012; van den Pol, 1982)”
From Parallel social information processing circuits are differentially impacted in autism (2020) · cites this paper as Dayanithi et al., 2012
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Neuropeptide Transmission in Brain Circuits
van den Pol, A. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.014 · Cited by 810 · see citing works
A secretagogin locus of the mammalian hypothalamus controls stress hormone release
Romanov, R. A., Alpár, A., Zhang, M., Zeisel, A., Calas, A., Landry, M., Fuszard, M., Shirran, S. L., Schnell, R., Dobolyi, Á., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201488977 · Cited by 85 · see citing works
Parallel social information processing circuits are differentially impacted in autism
Lewis, E. M., Stein-O’Brien, G. L., Patino, A. V., Nardou, R., Grossman, C. D., Brown, M., Bangamwabo, B., Ndiaye, N., Giovinazzo, D., Dardani, I., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.10.002 · Cited by 72 · see citing works
- Authors
- Dayanithi, G., Forostyak, O., Ueta, Y., Verkhratsky, A., & Toescu, E. C.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Czech Academy of Sciences (CZ)
- University of Occupational and Environmental Health Japan (JP)
- University of Birmingham (GB)
- Venue
- Cell Calcium
- Publisher
- Elsevier BV
- Published
- 2012-03
- Volume
- 51
- Issue
- 3-4
- Pages
- 293-299
- ISSN
- 0143-4160 (ISSN-L)
- OpenAlex
- W2066043959
- Cited by
- 38
- References
- 106
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 6 · 2019: 2 · 2018: 2 · 2017: 3 · 2016: 7 · 2015: 2 · 2014: 4 · 2013: 2 · 2012: 3
- FWCI
- 0.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell Calcium (publishedVersion)
- PubMed (publishedVersion)
- ASEP (submittedVersion, public-domain)
- Research Explorer (The University of Manchester) (submittedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Funders
- Grant Agency of the Czech Republic (GACR 303/11/0192)
- Centre National de la Recherche Scientifique
- Japanese Society for Promotion of Science Fellowship Programs
- Topics
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- calcium homeostasis, magnocellular neurons, supraoptic nucleus, paraventricular nucleus, neurohypophysis, vasopressin, oxytocin, neurohormone release, axonal terminals, Na+/Ca2+ exchanger, endoplasmic reticulum calcium stores, plasma membrane Ca2+ pump, mitochondrial calcium uptake
- MeSH terms
- Animals, Homeostasis, Humans, Nerve Endings, Neurosecretion, Oxytocin, Pituitary Gland, Vasopressins, Calcium Channels, Presynaptic Terminals, Calcium Signaling, Receptor Cross-Talk
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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