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10.1113/jphysiol.2010.201855

http://scihub22266oqcxt.onion/10.1113/jphysiol.2010.201855
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21135052!3099011!21135052
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suck abstract from ncbi

pmid21135052      J+Physiol 2011 ; 589 (Pt 7): 1515-25
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  • TRPM2: a multifunctional ion channel for calcium signalling #MMPMID21135052
  • Sumoza-Toledo A; Penner R
  • J Physiol 2011[Apr]; 589 (Pt 7): 1515-25 PMID21135052show ga
  • The transient potential receptor melastatin-2 (TRPM2) channel has emerged as an important Ca(2+) signalling mechanism in a variety of cells, contributing to cellular functions that include cytokine production, insulin release, cell motility and cell death. Its ability to respond to reactive oxygen species has made TRPM2 a potential therapeutic target for chronic inflammation, neurodegenerative diseases, and oxidative stress-related pathologies. TRPM2 is a non-selective, calcium (Ca(2+))-permeable cation channel of the melastatin-related transient receptor potential (TRPM) ion channel subfamily. It is activated by intracellular adenosine diphosphate ribose (ADPR) through a diphosphoribose hydrolase domain in its C-terminus and regulated through a variety of factors, including synergistic facilitation by [Ca(2+)](i), cyclic ADPR, H(2)O(2), NAADP, and negative feedback regulation by AMP and permeating protons (pH). In addition to its role mediating Ca(2+) influx into the cells, TRPM2 can also function as a lysosomal Ca(2+) release channel, contributing to cell death. The physiological and pathophysiological context of ROS-mediated events makes TRPM2 a promising target for the development of therapeutic tools of inflammatory and degenerative diseases.
  • |Alternative Splicing[MESH]
  • |Animals[MESH]
  • |Bipolar Disorder/physiopathology[MESH]
  • |Calcium Signaling/*physiology[MESH]
  • |Diabetes Mellitus, Type 2/physiopathology[MESH]
  • |Humans[MESH]
  • |Ion Channel Gating/physiology[MESH]
  • |Mice[MESH]
  • |Mice, Knockout[MESH]
  • |Models, Biological[MESH]
  • |Models, Molecular[MESH]


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