KCNK10

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KCNK10 (Potassium Two Pore Domain Channel Subfamily K Member 10), also known as TREK-2, is a protein that in humans is encoded by the KCNK10 gene. This gene is a member of the potassium channel family, specifically the two-pore-domain potassium channels (K2P channels). These channels contribute to the passive conductance of potassium ions across the cell membrane, playing a key role in setting the resting membrane potential and contributing to the electrical excitability of cells.

Function[edit | edit source]

KCNK10/TREK-2 channels are leak potassium channels, which means they are responsible for the background potassium current that helps to maintain the resting potential of the cell. They are activated by various physical and chemical stimuli, including temperature, pH changes, mechanical stretch, and lipids. This makes them important for cellular responses to environmental changes and for the regulation of neuronal excitability, pain perception, and anesthetic mechanisms.

Structure[edit | edit source]

The structure of KCNK10, like other members of the K2P channel family, features four transmembrane domains with two pore-forming P domains between the second and third transmembrane segments. This configuration allows the channel to form a dimer in the cell membrane, with each dimer containing two pore domains necessary for potassium ion conduction.

Clinical Significance[edit | edit source]

Alterations in the expression or function of KCNK10 have been implicated in various neurological disorders and diseases. For example, dysregulation of TREK-2 channels has been associated with pain disorders, epilepsy, and depression. Understanding the mechanisms of KCNK10 function and regulation could lead to new therapeutic targets for these conditions.

Genetic Information[edit | edit source]

The KCNK10 gene is located on chromosome 8 in humans. Variants and mutations within this gene can affect the expression and function of the TREK-2 channel, potentially leading to or exacerbating disease states.

Research[edit | edit source]

Ongoing research is focused on elucidating the detailed mechanisms of KCNK10 channel regulation, its role in various physiological processes, and its involvement in disease. Studies are also exploring the potential of targeting KCNK10 channels with drugs to treat related diseases, highlighting the therapeutic potential of modulating potassium channel activity.


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Contributors: Prab R. Tumpati, MD