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10.1007/s12975-020-00810-3

http://scihub22266oqcxt.onion/10.1007/s12975-020-00810-3
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32430797!ä!32430797

suck abstract from ncbi


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pmid32430797      Transl+Stroke+Res 2021 ; 12 (1): 164-184
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  • TRPM7 Mediates Neuronal Cell Death Upstream of Calcium/Calmodulin-Dependent Protein Kinase II and Calcineurin Mechanism in Neonatal Hypoxic-Ischemic Brain Injury #MMPMID32430797
  • Turlova E; Wong R; Xu B; Li F; Du L; Habbous S; Horgen FD; Fleig A; Feng ZP; Sun HS
  • Transl Stroke Res 2021[Feb]; 12 (1): 164-184 PMID32430797show ga
  • Transient receptor potential melastatin 7 (TRPM7), a calcium-permeable, ubiquitously expressed ion channel, is critical for axonal development, and mediates hypoxic and ischemic neuronal cell death in vitro and in vivo. However, the downstream mechanisms underlying the TRPM7-mediated processes in physiology and pathophysiology remain unclear. In this study, we employed a mouse model of hypoxic-ischemic brain cell death which mimics the pathophysiology of hypoxic-ischemic encephalopathy (HIE). HIE is a major public health issue and an important cause of neonatal deaths worldwide; however, the available treatments for HIE remain limited. Its survivors face life-long neurological challenges including mental retardation, cerebral palsy, epilepsy and seizure disorders, motor impairments, and visual and auditory impairments. Through a proteomic analysis, we identified calcium/calmodulin-dependent protein kinase II (CaMKII) and phosphatase calcineurin as potential mediators of cell death downstream from TRPM7 activation. Further analysis revealed that TRPM7 mediates cell death through CaMKII, calmodulin, calcineurin, p38, and cofilin cascade. In vivo, we found a significant reduction of brain injury and improvement of short- and long-term functional outcomes after HI after administration of specific TRPM7 blocker waixenicin A. Our data demonstrate a molecular mechanism of TRPM7-mediated cell death and identifies TRPM7 as a promising therapeutic and drug development target for HIE.
  • |Acetates/pharmacology[MESH]
  • |Animals[MESH]
  • |Animals, Newborn[MESH]
  • |Avoidance Learning/physiology[MESH]
  • |Calcineurin/*metabolism[MESH]
  • |Calcium-Calmodulin-Dependent Protein Kinase Type 2/*metabolism[MESH]
  • |Cell Death/drug effects/*physiology[MESH]
  • |Cells, Cultured[MESH]
  • |Diterpenes/pharmacology[MESH]
  • |Female[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Hypoxia-Ischemia, Brain/*metabolism/pathology[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Neurons/drug effects/*metabolism/pathology[MESH]


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