4.7 Review

Metabolic Basis of Creatine in Health and Disease: A Bioinformatics-Assisted Review

Journal

NUTRIENTS
Volume 13, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/nu13041238

Keywords

creatine kinase; energy metabolism; cell survival; bioinformatics; systems biology; cellular allostasis; dynamic biosensor

Funding

  1. AlzChem Tostberg GmbH

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Creatine is a vital molecule synthesized mainly in the liver, kidneys, and pancreas, with its transportation and metabolism playing a crucial role in cellular bioenergetics. The CK/PCr system, essential for cell survival and growth, acts as a dynamic biosensor based on chemo-mechanical energy transduction, impacting various tissues and contributing to a wide range of diseases through dysregulation in Cr metabolism.
Creatine (Cr) is a ubiquitous molecule that is synthesized mainly in the liver, kidneys, and pancreas. Most of the Cr pool is found in tissues with high-energy demands. Cr enters target cells through a specific symporter called Na+/Cl--dependent Cr transporter (CRT). Once within cells, creatine kinase (CK) catalyzes the reversible transphosphorylation reaction between [Mg2+:ATP(4-)](2-) and Cr to produce phosphocreatine (PCr) and [Mg2+:ADP(3-)](-). We aimed to perform a comprehensive and bioinformatics-assisted review of the most recent research findings regarding Cr metabolism. Specifically, several public databases, repositories, and bioinformatics tools were utilized for this endeavor. Topics of biological complexity ranging from structural biology to cellular dynamics were addressed herein. In this sense, we sought to address certain pre-specified questions including: (i) What happens when creatine is transported into cells? (ii) How is the CK/PCr system involved in cellular bioenergetics? (iii) How is the CK/PCr system compartmentalized throughout the cell? (iv) What is the role of creatine amongst different tissues? and (v) What is the basis of creatine transport? Under the cellular allostasis paradigm, the CK/PCr system is physiologically essential for life (cell survival, growth, proliferation, differentiation, and migration/motility) by providing an evolutionary advantage for rapid, local, and temporal support of energy- and mechanical-dependent processes. Thus, we suggest the CK/PCr system acts as a dynamic biosensor based on chemo-mechanical energy transduction, which might explain why dysregulation in Cr metabolism contributes to a wide range of diseases besides the mitigating effect that Cr supplementation may have in some of these disease states.

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