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The Role of Inositol Hexakisphosphate Kinase in the Central Nervous System

Overview
Journal Biomolecules
Publisher MDPI
Date 2023 Sep 28
PMID 37759717
Authors
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Abstract

Inositol is a unique biological small molecule that can be phosphorylated or even further pyrophosphorylated on each of its six hydroxyl groups. These numerous phosphorylation states of inositol along with the kinases and phosphatases that interconvert them comprise the inositol phosphate signaling pathway. Inositol hexakisphosphate kinases, or IP6Ks, convert the fully mono-phosphorylated inositol to the pyrophosphate 5-IP7 (also denoted IP7). There are three isoforms of IP6K: IP6K1, 2, and 3. Decades of work have established a central role for IP6Ks in cell signaling. Genetic and pharmacologic manipulation of IP6Ks in vivo and in vitro has shown their importance in metabolic disease, chronic kidney disease, insulin signaling, phosphate homeostasis, and numerous other cellular and physiologic processes. In addition to these peripheral processes, a growing body of literature has shown the role of IP6Ks in the central nervous system (CNS). IP6Ks have a key role in synaptic vesicle regulation, Akt/GSK3 signaling, neuronal migration, cell death, autophagy, nuclear translocation, and phosphate homeostasis. IP6Ks' regulation of these cellular processes has functional implications in vivo in behavior and CNS anatomy.

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References
1.
Clayton E, Sue N, Smillie K, OLeary T, Bache N, Cheung G . Dynamin I phosphorylation by GSK3 controls activity-dependent bulk endocytosis of synaptic vesicles. Nat Neurosci. 2010; 13(7):845-51. PMC: 2894011. DOI: 10.1038/nn.2571. View

2.
Moritoh Y, Abe S, Akiyama H, Kobayashi A, Koyama R, Hara R . The enzymatic activity of inositol hexakisphosphate kinase controls circulating phosphate in mammals. Nat Commun. 2021; 12(1):4847. PMC: 8358040. DOI: 10.1038/s41467-021-24934-8. View

3.
Boregowda S, Ghoshal S, Booker C, Krishnappa V, Chakraborty A, Phinney D . IP6K1 Reduces Mesenchymal Stem/Stromal Cell Fitness and Potentiates High Fat Diet-Induced Skeletal Involution. Stem Cells. 2017; 35(8):1973-1983. PMC: 5533188. DOI: 10.1002/stem.2645. View

4.
Li X, Gu C, Hostachy S, Sahu S, Wittwer C, Jessen H . Control of XPR1-dependent cellular phosphate efflux by InsP is an exemplar for functionally-exclusive inositol pyrophosphate signaling. Proc Natl Acad Sci U S A. 2020; 117(7):3568-3574. PMC: 7035621. DOI: 10.1073/pnas.1908830117. View

5.
Qi J, Cheng W, Gao Z, Chen Y, Shipton M, Furkert D . Itraconazole inhibits endothelial cell migration by disrupting inositol pyrophosphate-dependent focal adhesion dynamics and cytoskeletal remodeling. Biomed Pharmacother. 2023; 161:114449. PMC: 7614367. DOI: 10.1016/j.biopha.2023.114449. View