Literature DB >> 31073743

Role of the chanzyme TRPM7 in the nervous system in health and disease.

Nashat Abumaria1,2, Wei Li3, Andrew N Clarkson4.   

Abstract

The channel kinase (chanzyme) transient receptor potential melastatin-like 7 (TRPM7) has a unique dual protein structure composed of an ion channel with an α-kinase domain on its C-terminus. In the nervous system, under physiological conditions, TRPM7 contributes to critical neurobiological processes ranging from synaptic transmission to cognitive functions. Following certain pathological triggers, TRPM7 mediates neurotoxicity, neuro-injuries, and neuronal death. Here, we summarize the current knowledge of TRPM7 functions in neuronal systems in health and disease. The molecular mechanisms by which this chanzyme might regulate synaptic and cognitive functions are discussed. We also discuss the lack of knowledge regarding the molecular mechanisms responsible for turning TRPM7 into "a vicious tool" that mediates neuronal death following certain pathological triggers. Some synthetic and natural pharmacological modulators of the TRPM7 channel and its α-kinase are reviewed. We suggest that based on current knowledge, we should reshape our thinking regarding the implications of TRPM7 in neurological and neurodegenerative disorders. Moreover, we propose a paradigm shift concerning the targeting of TRPM7 as a therapeutic approach for treating certain neurological diseases. We agree that TRPM7 overexpression or overactivation may mediate neurodegenerative processes following certain triggers. However, TRPM7 dysfunction and/or downregulation might also be among the pathological changes leading to neurodegeneration. Consequently, further investigations are required before we decide whether blocking or activating the chanzyme is the correct therapeutic approach to treat certain neurological and/or neurodegenerative diseases.

Entities:  

Keywords:  Alzheimer’s disease; Cofilin; Learning and memory; Neurodegeneration; Parkinson’s disease; Synapse density; Synaptic plasticity

Mesh:

Substances:

Year:  2019        PMID: 31073743     DOI: 10.1007/s00018-019-03124-2

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  74 in total

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Authors:  L W Runnels; L Yue; D E Clapham
Journal:  Science       Date:  2001-01-18       Impact factor: 47.728

4.  Separation and characterization of currents through store-operated CRAC channels and Mg2+-inhibited cation (MIC) channels.

Authors:  Murali Prakriya; Richard S Lewis
Journal:  J Gen Physiol       Date:  2002-05       Impact factor: 4.086

5.  Disturbances of magnesium concentrations in various brain areas in Alzheimer's disease.

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Journal:  Magnes Res       Date:  2000-09       Impact factor: 1.115

6.  LTRPC7 is a Mg.ATP-regulated divalent cation channel required for cell viability.

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Journal:  Nature       Date:  2001-05-31       Impact factor: 49.962

7.  Characterization of the protein kinase activity of TRPM7/ChaK1, a protein kinase fused to the transient receptor potential ion channel.

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Review 8.  Why did NMDA receptor antagonists fail clinical trials for stroke and traumatic brain injury?

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Journal:  Lancet Neurol       Date:  2002-10       Impact factor: 44.182

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Authors:  Mahealani K Monteilh-Zoller; Meredith C Hermosura; Monica J S Nadler; Andrew M Scharenberg; Reinhold Penner; Andrea Fleig
Journal:  J Gen Physiol       Date:  2003-01       Impact factor: 4.086

10.  Distinct properties of CRAC and MIC channels in RBL cells.

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Journal:  J Gen Physiol       Date:  2002-08       Impact factor: 4.086

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Review 2.  Potential Implications of Mammalian Transient Receptor Potential Melastatin 7 in the Pathophysiology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Review.

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4.  Neuroprotective Effects of TRPM7 Deletion in Parvalbumin GABAergic vs. Glutamatergic Neurons following Ischemia.

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6.  1-L Transcription in Alzheimer's Disease.

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Review 7.  Role of TRPM2 in brain tumours and potential as a drug target.

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