Elevated serum magnesium lowers calcification propensity in Memo1-deficient mice

• Published in: PloS one Vol. 15; no. 7; p. e0236361
• Main Authors: Moor, Matthias B, Ramakrishnan, Suresh K, Legrand, Finola, Bachtler, Matthias, Koesters, Robert, Hynes, Nancy E, Pasch, Andreas, Bonny, Olivier, Friedman, Peter A
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 24.07.2020; Public Library of Science (PLoS)
• Subjects: Aging; Animal models; Biology and Life Sciences; Calcification; Channels; Diet; Epidermal growth factor; Experiments; Fibroblast growth factor 23; Gene expression; Genotype & phenotype; Growth factors; Health aspects; Homeostasis; Intestine; Kidneys; Klotho protein; Laboratories; Magnesium; Magnesium (Nutrient); Males; Medicine and Health Sciences; Metabolism; Methods; Mineral metabolism; Nephrology; Pathophysiology; Phenotypes; Phosphorus; Physical Sciences; Physiology; Proteins; Reabsorption; Research and Analysis Methods; Vitamin A; Vitamin D; Vitamin deficiency; Vitamin E; United States; Switzerland; Austria
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0236361

MEdiator of cell MOtility1 (MEMO1) is a ubiquitously expressed redox protein involved in extracellular ligand-induced cell signaling. We previously reported that inducible whole-body Memo1 KO (cKO) mice displayed a syndrome of premature aging and disturbed mineral metabolism partially recapitulating the phenotype observed in Klotho or Fgf23-deficient mouse models. Here, we aimed at delineating the contribution of systemic mineral load on the Memo1 cKO mouse phenotype. We attempted to rescue the Memo1 cKO phenotype by depleting phosphate or vitamin D from the diet, but did not observe any effect on survival. However, we noticed that, by contrast to Klotho or Fgf23-deficient mouse models, Memo1 cKO mice did not present any soft-tissue calcifications and displayed even a decreased serum calcification propensity. We identified higher serum magnesium levels as the main cause of protection against calcifications. Expression of genes encoding intestinal and renal magnesium channels and the regulator epidermal growth factor were increased in Memo1 cKO. In order to check whether magnesium reabsorption in the kidney alone was driving the higher magnesemia, we generated a kidney-specific Memo1 KO (kKO) mouse model. Memo1 kKO mice also displayed higher magnesemia and increased renal magnesium channel gene expression. Collectively, these data identify MEMO1 as a novel regulator of magnesium homeostasis and systemic calcification propensity, by regulating expression of the main magnesium channels.