MiR-139-5p inhibits HGTD-P and regulates neuronal apoptosis induced by hypoxia-ischemia in neonatal rats

Neurobiol Dis. 2014 Mar:63:184-93. doi: 10.1016/j.nbd.2013.11.023. Epub 2013 Dec 10.

Abstract

Human growth transformation dependent protein (HGTD-P) is a newly identified protein that promotes neuronal apoptosis in hypoxia-ischemia brain damage (HIBD) in neonatal rats. However, the mechanisms regulating HGTD-P expression are not clear. Here we describe microRNAs targeted to HGTD-P and examine their effects on regulating neuronal apoptosis in HIBD. We use samples from cultured neurons after oxygen-glucose deprivation (OGD) and postnatal day 10 rat brains after hypoxia-ischemia (HI). RT-PCR, Western blotting, and immunostaining are used to detect the expression of HGTD-P and cleaved caspase 3, as well as real-time PCR detects microRNA expression. MicroRNA agomir is used to inhibit the expression of HGTD-P, and DAPI, TUNEL, and TTC staining are employed to detect cell apoptosis and brain damage. Moreover, in vitro processing assay is used to examine the mechanism by which HI down-regulates miR-139-5p expression. We found that miR-139-5p is down-regulated in neurons and rat brains after HI treatment. The expression pattern of miR-139-5p correlates inversely with that of HGTD-P. Furthermore, miR-139-5p agomir inhibits neuronal apoptosis and attenuates HIBD, which is concurrent with down-regulation of HGTD-P. Moreover, pre-miR-139 processing activity decreases in extracts from OGD neurons, and OGD neuronal extracts attenuates the processing of pre-miR-139 by Dicer. In conclusion, HI induces inhibitors which block the processing step of pre-miR-139, resulting in the down-regulation of mature miR-139-5p. The down-regulation of miR-139-5p plays a critical role in the up-regulation of HGTD-P expression. MiR-139-5p agomir attenuates brain damage when used 12h after HI, providing a longer therapeutic window than anti-apoptosis compounds currently available.

Keywords: 3′-untranslated regions; 3′UTR; AI; AIF; Apoptosis; Brain; CC3; CCA; HGTD-P; HI; HIBD; Hypoxia–ischemia; MicroRNA; OGD; RISC; RNA-induced silencing complex; TTC; apoptosis inducible factor; apoptotic index; cleaved caspase 3; common carotid artery; human growth transformation dependent protein; hypoxia–ischemia; hypoxia–ischemia brain damage; oxygen–glucose deprivation; tPA; tissue plasminogen activator; triphenyltetrazolium chloride.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis / drug effects
  • Apoptosis / radiation effects*
  • Brain Infarction / etiology
  • Brain Infarction / pathology
  • Cells, Cultured
  • Disease Models, Animal
  • Embryo, Mammalian
  • Gene Expression Regulation / genetics
  • Gene Expression Regulation / physiology*
  • Glucose / deficiency
  • Humans
  • Hypoxia / metabolism
  • Hypoxia-Ischemia, Brain / pathology*
  • Membrane Proteins / metabolism*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Mitochondrial Proteins / metabolism*
  • Morpholinos / pharmacology
  • Neurons / cytology
  • Neurons / metabolism*
  • Phosphopyruvate Hydratase / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors

Substances

  • FAM162A protein, human
  • MIRN139 microRNA, human
  • Membrane Proteins
  • MicroRNAs
  • Mitochondrial Proteins
  • Morpholinos
  • Phosphopyruvate Hydratase
  • Glucose