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      The newest TRP channelopathy: Gain of function TRPM3 mutations cause epilepsy and intellectual disability

      review-article
      ,
      Channels
      Taylor & Francis
      TRPM3, Channelopathy, Epilepsy, TRP channel

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          ABSTRACT

          Transient Receptor Potential Melastatin 3 (TRPM3) is a Ca 2+ permeable nonselective cation channel, activated by heat and chemical agonists, such as the endogenous neuro-steroid Pregnenolone Sulfate (PregS) and the chemical compound CIM0216. TRPM3 is expressed in peripheral sensory neurons of the dorsal root ganglia (DRG), and its role in noxious heat sensation in mice is well established. TRPM3 is also expressed in a number of other tissues, including the brain, but its role there has been largely unexplored. Recent reports showed that two mutations in TRPM3 are associated with a developmental and epileptic encephalopathy, pointing to an important role of TRPM3 in the human brain. Subsequent reports found that the two disease-associated mutations increased basal channel activity, and sensitivity of the channel to activation by heat and chemical agonists. This review will discuss these mutations in the context of human diseases caused by mutations in other TRP channels, and in the context of the biophysical properties and physiological functions of TRPM3.

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          Most cited references84

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          An introduction to TRP channels.

          The aim of this review is to provide a basic framework for understanding the function of mammalian transient receptor potential (TRP) channels, particularly as they have been elucidated in heterologous expression systems. Mammalian TRP channel proteins form six-transmembrane (6-TM) cation-permeable channels that may be grouped into six subfamilies on the basis of amino acid sequence homology (TRPC, TRPV, TRPM, TRPA, TRPP, and TRPML). Selected functional properties of TRP channels from each subfamily are summarized in this review. Although a single defining characteristic of TRP channel function has not yet emerged, TRP channels may be generally described as calcium-permeable cation channels with polymodal activation properties. By integrating multiple concomitant stimuli and coupling their activity to downstream cellular signal amplification via calcium permeation and membrane depolarization, TRP channels appear well adapted to function in cellular sensation. Our review of recent literature implicating TRP channels in neuronal growth cone steering suggests that TRPs may function more widely in cellular guidance and chemotaxis. The TRP channel gene family and its nomenclature, the encoded proteins and alternatively spliced variants, and the rapidly expanding pharmacology of TRP channels are summarized in online supplemental material.
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            A TRP channel trio mediates acute noxious heat sensing

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              Adult epilepsy.

              The epilepsies are one of the most common serious brain disorders, can occur at all ages, and have many possible presentations and causes. Although incidence in childhood has fallen over the past three decades in developed countries, this reduction is matched by an increase in elderly people. Monogenic Mendelian epilepsies are rare. A clinical syndrome often has multiple possible genetic causes, and conversely, different mutations in one gene can lead to various epileptic syndromes. Most common epilepsies, however, are probably complex traits with environmental effects acting on inherited susceptibility, mediated by common variation in particular genes. Diagnosis of epilepsy remains clinical, and neurophysiological investigations assist with diagnosis of the syndrome. Brain imaging is making great progress in identifying the structural and functional causes and consequences of the epilepsies. Current antiepileptic drugs suppress seizures without influencing the underlying tendency to generate seizures, and are effective in 60-70% of individuals. Pharmacogenetic studies hold the promise of being able to better individualise treatment for each patient, with maximum possibility of benefit and minimum risk of adverse effects. For people with refractory focal epilepsy, neurosurgical resection offers the possibility of a life-changing cure. Potential new treatments include precise prediction of seizures and focal therapy with drug delivery, neural stimulation, and biological grafts.
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                Author and article information

                Journal
                Channels (Austin)
                Channels (Austin)
                Channels
                Taylor & Francis
                1933-6950
                1933-6969
                14 April 2021
                2021
                14 April 2021
                : 15
                : 1
                : 386-397
                Affiliations
                [0001]Department of Pharmacology, Physiology and Neuroscience, Rutgers, New Jersey Medical School; , Newark, NJ, USA
                Author notes
                CONTACT Tibor Rohacs tibor.rohacs@ 123456rutgers.edu Department of Pharmacology, Physiology and Neuroscience, Rutgers, New Jersey Medical School; , 185 South Orange Avenue, Newark, NJ07103, USA
                Author information
                https://orcid.org/0000-0003-3580-2575
                Article
                1908781
                10.1080/19336950.2021.1908781
                8057083
                33853504
                9feadc38-4fe0-4328-9a15-8bc9463269af
                © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Figures: 2, Tables: 1, References: 84, Pages: 12
                Categories
                Review
                Review

                Molecular biology
                trpm3,channelopathy,epilepsy,trp channel
                Molecular biology
                trpm3, channelopathy, epilepsy, trp channel

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