Journal
NEURAL REGENERATION RESEARCH
Volume 17, Issue 1, Pages 144-+Publisher
WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.314114
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Funding
- National Natural Science Foundation of China [81771346, 82071383]
- Taishan Scholar Program of Shandong Province of China [tsqn201812156]
- Spring City Leader Talent Support Plan [201984]
- Rongxiang Regenerative Medicine Foundation of Shandong University [2019SDRX-23]
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This study identified differentially expressed circRNAs and miRNAs in a mouse model of spinal cord injury, and found that circPrkcsh regulates the expression of miR-488 and the inflammation-related gene Ccl2. CircRNAs may play a role in the inflammatory response after spinal cord injury and could potentially be used as therapeutic targets for SCI.
Circular RNAs (circRNAs) are a class of conserved, endogenous non-coding RNAs that are involved in transcriptional and post-transcriptional gene regulation and are highly enriched in the nervous system. They participate in the survival and differentiation of multiple nerve cells, and may even promote the recovery of neurological function after stroke. However, their role in the inflammatory response after spinal cord injury remains unclear. In the present study, we established a mouse model of T9 spinal cord injury using the modified Allen's impact method, and identified 16,013 circRNAs and 960 miRNAs that were differentially expressed after spinal cord injury. Of these, the expression levels of circPrkcsh were significantly different between injured and sham-treated mice. We then treated astrocytes with tumor necrosis factor-alpha in vitro to simulate the inflammatory response after spinal cord injury. Our results revealed an elevated expression of circPrkcsh with a concurrent decrease in miR-488 expression in injured cells. We also found that circPrkcsh regulated the expression of the inflammation-related gene Ccl2. Furthermore, in tumor necrosis factor-alpha-treated astrocytes, circPrkcsh knockdown decreased the expression of Ccl2 by upregulating miR-488 expression, and reduced the secretion of inflammatory cytokines in vitro. These findings suggest that differentially expressed circRNAs participate in the inflammatory response after spinal cord injury and act as the regulators of certain microRNAs. Furthermore, circPrkcsh may be used as an miR-488 sponge to regulate Ccl2 expression, which might provide a new potential therapy for SCI. The study was approved by the Animal Ethics Committee of Shandong University of China (approval No. KYLL-20170303) on March 3, 2017.
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