Characteristics of cytokines in the sciatic nerve stumps and DRGs after rat sciatic nerve crush injury

• Published in: Military medical research 2020-11, Vol.7 (1), p.57-57, Article 57
• Main Authors: Zhang, Rui-Rui, Chen, Sai-Ling, Cheng, Zhang-Chun, Shen, Yin-Ying, Yi, Sheng, Xu, Hui
• Format: Article
• Language: English
• Subjects: Animals; Cytokines; Cytokines - pharmacology; Cytokines - therapeutic use; Disease Models, Animal; Genes; Inflammation; Injuries; Nerve Crush - methods; Nervous system; Neuralgia - drug therapy; Rats; Rats, Sprague-Dawley; Sciatic Nerve - drug effects; Statistical analysis; Surgery
• ISSN: 2054-9369; 2095-7467; 2054-9369
• DOI: 10.1186/s40779-020-00286-0

Cytokines are essential cellular modulators of various physiological and pathological activities, including peripheral nerve repair and regeneration. However, the molecular changes of these cellular mediators after peripheral nerve injury are still unclear. This study aimed to identify cytokines critical for the regenerative process of injured peripheral nerves. The sequencing data of the injured nerve stumps and the dorsal root ganglia (DRGs) of Sprague-Dawley (SD) rats subjected to sciatic nerve (SN) crush injury were analyzed to determine the expression patterns of genes coding for cytokines. PCR was used to validate the accuracy of the sequencing data. A total of 46, 52, and 54 upstream cytokines were differentially expressed in the SNs at 1 day, 4 days, and 7 days after nerve injury. A total of 25, 28, and 34 upstream cytokines were differentially expressed in the DRGs at these time points. The expression patterns of some essential upstream cytokines are displayed in a heatmap and were validated by PCR. Bioinformatic analysis of these differentially expressed upstream cytokines after nerve injury demonstrated that inflammatory and immune responses were significantly involved. In summary, these findings provide an overview of the dynamic changes in cytokines in the SNs and DRGs at different time points after nerve crush injury in rats, elucidate the biological processes of differentially expressed cytokines, especially the important roles in inflammatory and immune responses after peripheral nerve injury, and thus might contribute to the identification of potential treatments for peripheral nerve repair and regeneration.