The Time Sequence of Gene Expression Changes after Spinal Cord Injury

Cells. 2022 Jul 18;11(14):2236. doi: 10.3390/cells11142236.

Abstract

Gene expression changes following spinal cord injury (SCI) are time-dependent, and an accurate understanding of these changes can be crucial in determining time-based treatment options in a clinical setting. We performed RNA sequencing of the contused spinal cord of rats at five different time points from the very acute to chronic stages (1 hour, 1 day, 1 week, 1 month, and 3 months) following SCI. We identified differentially expressed genes (DEGs) and Gene Ontology (GO) terms at each time point, and 14,257 genes were commonly expressed at all time points. The biological process of the inflammatory response was increased at 1 hour and 1 day, and the cellular component of the integral component of the synaptic membrane was increased at 1 day. DEGs associated with cell activation and the innate immune response were highly enriched at 1 week and 1 month, respectively. A total of 2841 DEGs were differentially expressed at any of the five time points, and 18 genes (17 upregulated and 1 downregulated) showed common expression differences at all time points. We found that interleukin signaling, neutrophil degranulation, eukaryotic translation, collagen degradation, LGI-ADAM interactions, GABA receptor, and L1CAM-ankyrin interactions were prominent after SCI depending on the time post injury. We also performed gene-drug network analysis and found several potential antagonists and agonists which can be used to treat SCI. We expect to discover effective treatments in the clinical field through further studies revealing the efficacy and safety of potential drugs.

Keywords: RNA sequencing; gene ontology; small molecules; spinal cord injury; time sequence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression
  • Gene Expression Profiling*
  • Gene Ontology
  • Gene Regulatory Networks
  • Rats
  • Spinal Cord Injuries* / genetics
  • Spinal Cord Injuries* / metabolism

Grants and funding

This study was supported by grants (2019R1A6A1A11034536, 2020R1A2C2004764) through the National Research Foundation (NRF) and Ministry of Science and ICT (MSIT) and a Korea Medical Device Development Fund grant (202017D01) funded by the Korean government (MSIT, the Ministry of Trade, Industry and Energy, the Ministry of Health & Welfare, and the Ministry of Food and Drug Safety).