Magnesium transporter

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cora mag
mgta-b mag
MGTE
MRS2 LPE10 topology
XNTA topology

Magnesium Transporter refers to a class of proteins and molecular mechanisms responsible for the movement of magnesium ions (Mg2+) across cellular membranes. Magnesium is a crucial element for numerous biological processes, including DNA synthesis, RNA transcription, protein synthesis, and as a cofactor for many enzymes. Due to its importance, the regulation of magnesium levels within cells and across the body is tightly controlled by various magnesium transporters.

Types of Magnesium Transporters

Magnesium transporters can be broadly classified into several families based on their structure and mechanism of action. These include:

  • TRPM6 and TRPM7 Channels - Members of the transient receptor potential melastatin subfamily, these channels are involved in magnesium uptake in cells and are essential for magnesium homeostasis.
  • MagT1 and TUSC3 - These are transporter proteins that play roles in magnesium uptake, especially in cells of the immune system.
  • SLC41 Family - This family of solute carriers facilitates magnesium transport across the cell membrane.
  • CNNM Family - Cyclin and CBS domain divalent metal cation transport mediators, involved in the efflux and influx of magnesium ions.
  • MRS2 - Located in the mitochondrial membrane, it is crucial for magnesium homeostasis within mitochondria, affecting energy production and metabolism.

Function and Regulation

Magnesium transporters are vital for maintaining intracellular and extracellular magnesium levels. They are involved in processes such as:

The regulation of magnesium transporters is complex and involves various factors, including dietary magnesium intake, hormones such as estrogen and parathyroid hormone, and the magnesium status of the body.

Clinical Significance

Abnormalities in magnesium transport can lead to various health issues, including:

  • Hypomagnesemia - A condition characterized by low levels of magnesium in the blood, which can cause muscle spasms, seizures, and cardiovascular problems.
  • Hypermagnesemia - Elevated magnesium levels, which can lead to muscle weakness, low blood pressure, and cardiac arrest in severe cases.
  • Genetic disorders affecting magnesium transporters, such as mutations in the TRPM6 gene, can lead to familial hypomagnesemia with secondary hypocalcemia.

Understanding the mechanisms of magnesium transporters has implications for the treatment of these conditions and for enhancing overall health through better management of magnesium levels in the body.

Research Directions

Research in the field of magnesium transport continues to explore the detailed mechanisms of action of various magnesium transporters, their regulation, and their roles in health and disease. This includes studying the impact of genetic variations on transporter function and the potential for targeting magnesium transporters in therapeutic interventions for conditions related to magnesium imbalance.

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Contributors: Prab R. Tumpati, MD