4.4 Article

Up-regulation of protective neuronal MicroRNAs by FTY720 and novel FTY720-derivatives

期刊

NEUROSCIENCE LETTERS
卷 690, 期 -, 页码 178-180

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2018.10.040

关键词

Neuroprotection; Dopaminergic MN9D cells; miRNA upregulation

资金

  1. Texas Tech University Health Sciences Center El Paso Graduate School of Biomedical Sciences
  2. Fogarty International Center - U.S./Costa Rica Neuropsychiatric Genetics Research Training Program [NCOD-5D43TW008333]
  3. Hoy Family Research
  4. Perez Family Research
  5. Lizanell and Colbert Coldwell Foundation
  6. Ms. Anna Mae Doyle Gift Funds
  7. Multiple System Atrophy (MSA) Coalition
  8. El Paso Community Foundation

向作者/读者索取更多资源

In searching for Parkinson's disease (PD) pharmacotherapies we began studying FTY720, a food and drug administration (FDA) approved drug. We also created derivatives, FTY720-C2 and FTY720-Mitoxy, and began assessing them. Here we treated dopaminergic MN9D cells with FTY720s then measured microRNA (miRNA) levels by PCR arrays. We discovered that all three FTY720s increased miR376b-3p, while FTY720-C2 also increased miR-128-3p, miR-146b-5p, miR-7a-5p, and miR-9-5p, and FTY720-Mitoxy also increased miR-30d-5p. Investigations revealed that some miRNAs downregulate alpha-synuclein, while others reduce apoptosis, suggesting that FTY720s may act to reduce synucleinopathy and dopaminergic neuron loss in PD and related disorders.

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