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10.1007/s12031-016-0828-2

http://scihub22266oqcxt.onion/10.1007/s12031-016-0828-2
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suck abstract from ncbi


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pmid27631550      J+Mol+Neurosci 2016 ; 60 (4): 445-452
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  • Neuroprotective Role of MicroRNA-22 in a 6-Hydroxydopamine-Induced Cell Model of Parkinson s Disease via Regulation of Its Target Gene TRPM7 #MMPMID27631550
  • Yang CP; Zhang ZH; Zhang LH; Rui HC
  • J Mol Neurosci 2016[Dec]; 60 (4): 445-452 PMID27631550show ga
  • Parkinson's disease (PD), the second most prevalent neurodegenerative disorder with only symptomatic treatment available, is characterized by a progressive loss of dopaminergic neurons in the midbrain. Ample evidence indicated that microRNAs (miRs) could regulate post-transcriptional gene expression and neuronal disease. In the present study, we have evaluated the effects and mechanism of miR-22 in PC12 pheochromocytoma cells treated with 6-hydroxydopamine (6-OHDA) to mimic PD. RT-PCR results showed that the expression of miR-22 is downregulated in 6-OHDA-treated PC12 cells, and the overexpression of miR-22 significantly promoted the survival and proliferation of 6-OHDA-induced PC12 cells, whereas miR-22 inhibitor reversed these effects. In addition, PC12 cells were treated with miR-22 mimics or inhibitor following 6-OHDA administration, which medicated ROS production and upregulation or downregulation of caspase-3 activity, respectively. A luciferase reporter assay revealed that transient receptor potential melastatin 7 (TRPM7) is a direct target gene of miR-22, and miR-22 overexpression markedly downregulated the level of TRPM7. Strikingly, further analysis showed that miR-22 mediated 6-OHDA-induced PC12 cell survival and proliferation by targeting TRPM7. Taken together, the present study showed that miR-22 overexpression exhibited neuroprotective and reversal effects on the 6-OHDA-induced PC12 cell growth and apoptosis by targeting TRPM7.
  • |Animals[MESH]
  • |Apoptosis[MESH]
  • |Cell Proliferation[MESH]
  • |Cell Survival[MESH]
  • |Down-Regulation[MESH]
  • |Humans[MESH]
  • |MicroRNAs/*genetics/metabolism[MESH]
  • |Neurons/drug effects/metabolism[MESH]
  • |Oxidopamine/toxicity[MESH]
  • |PC12 Cells[MESH]
  • |Parkinson Disease/*metabolism[MESH]
  • |Protein Serine-Threonine Kinases/genetics/*metabolism[MESH]
  • |Rats[MESH]


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