1. Inorganic polyphosphate regulates functions of thymocytes via activation of P2X purinoreceptors.
- Author
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Nebesnaya KS, Makhmudov AR, Rustamov KR, Rakhmatullina NSH, Rustamova SI, Mirkhodjaev UZ, Charishnikova OS, Sabirov RZ, and Baev AY
- Subjects
- Animals, Molecular Docking Simulation, Thymocytes metabolism, Signal Transduction, Mammals metabolism, Calcium metabolism, Polyphosphates pharmacology
- Abstract
Inorganic polyphosphate (polyP) is an ancient polymer, which was proven to be a signalling molecule in the mammalian brain, mediating the communication between astrocytes via activation of P2Y
1 purinoreceptors and modulating the activity of neurons. There is very limited information regarding the ability of polyP to transmit the information as an agonist of purinoreceptors in other cells and tissues. Here, we show that application of polyP to the suspension of primary thymocytes increases the concentration of intracellular calcium. PolyP evoked calcium signal was dependent on the presence of P2X inhibitors but not P2Y1 inhibitor. PolyP dependent increase in intracellular calcium concentration caused mild mitochondrial depolarization, which was dependent on inhibitors of purinoreceptors, extracellular calcium and inhibitor of mitochondrial calcium uniporter but wasn't dependent on cyclosporin A. Application of polyP modulated cell volume regulation machinery of thymocytes in calcium dependent manner. Molecular docking experiments revealed that polyP can potentially bind to several types of P2X receptors with binding energy similar to ATP - natural agonist of P2X purinoreceptors. Further molecular dynamics simulations with P2X4 showed that binding of one molecule of polyP dramatically increases permeability of this receptor-channel for water molecules. Thus, in this research we for the first time showed that polyP can interact with P2X receptors in thymocytes and modulate physiological processes., Competing Interests: Declaration of Competing Interest The authors declare that there are no competing interests associated with the manuscript., (Copyright © 2023. Published by Elsevier B.V.)- Published
- 2024
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