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10.1002/jcb.29381

http://scihub22266oqcxt.onion/10.1002/jcb.29381
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31512791!ä!31512791

suck abstract from ncbi


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pmid31512791      J+Cell+Biochem 2020 ; 121 (2): 1452-1462
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  • Magnesium protects mouse hippocampal HT22 cells against hypoxia-induced injury by upregulation of miR-221 #MMPMID31512791
  • Mi F; Liu F; Zhang C
  • J Cell Biochem 2020[Feb]; 121 (2): 1452-1462 PMID31512791show ga
  • Magnesium (Mg(2+) ) has been shown to exert neuroprotective effects against hypoxia. However, it still remains elusive whether Mg(2+) protected mouse hippocampal HT22 cells against hypoxia-evoked damages. Therefore, we aimed to investigate the function of Mg(2+) and mechanisms associated with microRNA-221 (miR-221). HT22 cells were exposed to 3% O(2) for 24 hours to induce hypoxic damages with 21% as a normoxic culture condition. The damages were monitored by viability, migration, and apoptosis of HT22 cells with or without Mg(2+) pretreatment. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was applied to examine the alteration of miR-221, miR-210, and miR-17-5p. Transduction was carried out to artificially alter the expression of miR-221 and nerve growth factor (NGF), which was confirmed by qRT-PCR or Western blot assays. To blunt phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) and nuclear factor kappaB (NF-kappaB), LY294002 (10 microM) and BAY 11-7082 (10 microM) were used. We observed Mg(2+) protected HT22 cells against hypoxia-induced damages by upregulating miR-221. Further, miR-221 positively regulated NGF expression. Overexpression of NGF alleviated cell injury, while suppression of NGF aggravated cell injury. Moreover, miR-221 elevated NGF by inducing phosphorylation of regulators in PI3K/AKT and NF-kappaB transduction cascades and then alleviated cell injury. In conclusion, Mg(2+) protected HT22 cells against hypoxia-induced damages by upregulation of miR-221 and NGF. These findings provided insights into the development of improved strategies for clinical application.
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