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

被引:29
|
作者
Abumaria, Nashat [1 ,2 ,3 ]
Li, Wei [1 ,2 ]
Clarkson, Andrew N. [4 ,5 ]
机构
[1] Fudan Univ, Inst Brain Sci, State Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[2] Fudan Univ, MOE Frontiers Ctr Brain Sci, Inst Brain Sci, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Lab Anim Sci, Shanghai 200032, Peoples R China
[4] Brain Hlth Res Ctr, Dept Anat, POB 913, Dunedin 9054, New Zealand
[5] Brain Res New Zealand, POB 913, Dunedin 9054, New Zealand
关键词
Alzheimer's disease; Cofilin; Learning and memory; Neurodegeneration; Parkinson's disease; Synapse density; Synaptic plasticity; ION-CHANNEL; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; BRAIN; MAGNESIUM; KINASE; NEURONS; PROTEIN; ACTIVATION; INHIBITOR;
D O I
10.1007/s00018-019-03124-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The channel kinase (chanzyme) transient receptor potential melastatin-like 7 (TRPM7) has a unique dual protein structure composed of an ion channel with an alpha-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 alpha-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.
引用
收藏
页码:3301 / 3310
页数:10
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