4.4 Article

Altered long noncoding RNA expressions in dorsal root ganglion after rat sciatic nerve injury

Journal

NEUROSCIENCE LETTERS
Volume 534, Issue -, Pages 117-122

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2012.12.014

Keywords

Long noncoding RNA; Dorsal root ganglion; Nerve regeneration

Categories

Funding

  1. 863 Program [2012AA020502]
  2. National Natural Science Foundation of China [81130080, 81171180]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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Dorsal root ganglia (DRG) neurons spontaneously undergo robust neurite growth after axotomy. Long noncoding RNAs (lncRNAs) are an important class of pervasive genes involved in a variety of biological functions. However, the functions of lncRNAs in the regulation of responses of DRG neurons to injury stimuli remain untested. Here, lncRNA microarray analysis was performed to profile the lncRNAs in L4-L6 DRGs following rat sciatic nerve resection. The 105 lncRNAs were identified to be differentially expressed at 0, 1, 4, 7 d post injury. A coexpression network of 24 down-regulated lncRNAs and coding genes was constructed, and 115 targets of these 24 lncRNAs were found to be mainly involved in cell phenotype modulation, including glial cell migration, purinergic nucleotide receptor signaling pathway, vasodilation, regulation of multi-organism process, and neuropeptide signaling pathway, and also to be potentially associated with several key regeneration signaling pathways, including MAPK signaling pathway, and neuroactive ligand-receptor interaction. LncRNA BC089918 was selected from 24 down-regulated lncRNAs for validation by quantitative real-time polymerase chain reaction and in situ hybridization. And silencing of BC089918 with small interfering RNAs indicted that the lncRNA had a particular promoting effect on neurite outgrowth. Our data demonstrated a distinct involvement of lncRNAs in DRGs after nerve injury, thus contributing to illustration of molecular mechanisms responsible for nerve regeneration. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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