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Control of Ca2+ and metabolic homeostasis by the Na+/Ca2+ exchangers (NCXs) in health and disease

期刊

BIOCHEMICAL PHARMACOLOGY
卷 203, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2022.115163

关键词

Calcium; Glutamate; Metabolism; Mitochondria; NCX; Sodium

资金

  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [FAPESP 2018/25747-5]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [CNPq 312020/2019-8]
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [001]
  4. Ministero dell'Istruzione, dell'Universit'a e della Ricerca (MIUR) [2017YH3SXK]
  5. Ricerca Scientifica di Ateneo (RSA) from the University Politecnica delle Marche
  6. FFABR grant (2017) from MIUR

向作者/读者索取更多资源

Spatial and temporal control of calcium levels is crucial for cell activities. Na+/Ca2+ exchangers (NCXs) play a role in maintaining calcium homeostasis and supporting cellular metabolism. Preserving a timed and balanced NCX activity has therapeutic potential for various diseases.
Spatial and temporal control of calcium (Ca2+) levels is essential for the background rhythms and responses of living cells to environmental stimuli. Whatever other regulators a given cellular activity may have, localized and wider scale Ca2+ events (sparks, transients, and waves) are hierarchical determinants of fundamental processes such as cell contraction, excitability, growth, metabolism and survival. Different cell types express specific channels, pumps and exchangers to efficiently generate and adapt Ca2+ patterns to cell requirements. The Na+/Ca2+ exchangers (NCXs) in particular contribute to Ca2+ homeostasis by buffering intracellular Ca2+ loads ac-cording to the electrochemical gradients of substrate ions - i.e., Ca2+ and sodium (Na+) - and under a dynamic control of redundant regulatory processes. An interesting feature of NCX emerges from the strict relationship that connects transporter activity with cell metabolism: on the one hand NCX operates under constant control of ATP -dependent regulatory processes, on the other hand the ion fluxes generated through NCX provide mechanistic support for the Na+-driven uptake of glutamate and Ca2+ influx to fuel mitochondrial respiration. Proof of concept evidence highlights therapeutic potential of preserving a timed and balanced NCX activity in a growing rate of diseases (including excitability, neurodegenerative, and proliferative disorders) because of an improved ability of stressed cells to safely maintain ion gradients and mitochondrial bioenergetics. Here, we will summarize and review recent works that have focused on the pathophysiological roles of NCXs in balancing the two-way relationship between Ca2+ signals and metabolism.

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